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Subject to completion, as filed with the Securities and Exchange Commission on January 9, 2019.

Registration No. 333-

UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549

FORM S-1
REGISTRATION STATEMENT
UNDER
THE SECURITIES ACT OF 1933

AQUAMED TECHNOLOGIES, INC.

(Exact name of Registrant as Specified in its Charter)

	Delaware			3841			26-4042544
	(State or other jurisdiction of incorporation or organization)			(Primary Standard Industrial Classification Code Number)			(I.R.S. Employer Identification Number)

2150 Cabot Boulevard, West
Suite B
Langhorne, Pennsylvania 19067
(215) 702-8550
(Address, including zip code, and telephone number, including
area code, of Registrant’s principal executive offices)

David Johnson
Chief Executive Officer
AquaMed Technologies, Inc.
2150 Cabot Boulevard, West
Suite B
Langhorne, Pennsylvania 19067
(215) 702-8550
(Name, address, including zip code, and telephone number, including area code, of agent for service)

With copies to:

Rick A. Werner, Esq.
Haynes & Boone, LLP
30 Rockefeller Plaza, 26th Floor
New York, NY 10112
(212) 659-7300

Neil M. Kaufman
Kaufman & Associates, LLC
190 Motor Parkway, Suite 202
Hauppauge, NY 11788
(631) 972-0042

Approximate date of commencement of proposed sale to the public:
As soon as practicable after this Registration Statement becomes effective and the satisfaction of all other conditions to the completion of the transactions described in the enclosed document have been satisfied or waived.

If any of the securities being registered on this Form are to be offered on a delayed or continuous basis pursuant to Rule 415 under the Securities Act of 1933, check the following box. ☐

If this Form is filed to register additional securities for an offering pursuant to Rule 462(b) under the Securities Act, check the following box and list the Securities Act registration statement number of the earlier effective registration statement for the same offering. ☐

If this Form is a post-effective amendment filed pursuant to Rule 462(c) under the Securities Act, check the following box and list the Securities Act registration statement number of the earlier effective registration statement for the same offering. ☐

If this Form is a post-effective amendment filed pursuant to Rule 462(d) under the Securities Act, check the following box and list the Securities Act registration statement number of the earlier effective registration statement for the same offering. ☐

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, smaller reporting company or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company” and “emerging growth company” in Rule 12b-2 of the Exchange Act. (Check one):

	Large accelerated filer ☐			Accelerated filer ☐			Non-accelerated filer ☒			Smaller reporting company ☒
										Emerging growth company ☒

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 7(a)(2)(B) of the Securities Act. ☐

CALCULATION OF REGISTRATION FEE

Title of Each Class of Securities to be Registered

Amount to be
Registered(1)

Proposed Maximum
Offering Price
Per Share(1)

Proposed Maximum
Aggregate
Offering Price(2)

Amount of
Registration Fee(3)

Common Stock, par value $0.001 per share

1,750,000

N/A

539,000

65.33

(1)

This Registration Statement relates to shares of common stock, par value $0.001 per share, of AquaMed Technologies, Inc., which we refer to as AquaMed or the Company, which will be distributed pursuant to a spin-off transaction to a third-party distribution agent for the benefit of holders of shares of common stock, par value $0.001 per share, of Alliqua BioMedical, Inc., which we refer to as Alliqua. The amount of AquaMed common stock to be registered represents the maximum number of shares of AquaMed common stock that will be distributed to the third-party distribution agent for the benefit of holders of Alliqua common stock upon consummation of the spin-off.

(2)

Estimated solely for purposes of calculating the registration fee pursuant to Rule 457(f)(2) of the Securities Act, based on the book value (computed as of September 30, 2018, the most recent date for which such information is available) of the common stock of AquaMed.

(3)

Computed in accordance with Rule 457(f) and Section 6(b) under the Securities Act of 1933 by multiplying (A) the proposed maximum aggregate offering price for all securities to be registered by (B) 0.0001212.

The Registrant hereby amends this Registration Statement on such date or dates as may be necessary to delay its effective date until the Registrant shall file a further amendment which specifically states that this Registration Statement shall thereafter become effective in accordance with Section 8(a) of the Securities Act of 1933, or until the Registration Statement shall become effective on such date as the Securities and Exchange Commission, acting pursuant to said Section 8(a), may determine.

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The information in this prospectus is not complete and may be changed. We may not issue these securities until the registration statement filed with the Securities and Exchange Commission is effective. This prospectus is not an offer to sell these securities and is not soliciting an offer to buy these securities in any state where the offer or sale is not permitted.

Subject to Completion, dated January 9, 2019

PRELIMINARY PROSPECTUS

1,750,000 shares

AquaMed Technologies, Inc.

Common Stock

(par value $0.001 per share)

This prospectus is being furnished in connection with the planned distribution by Alliqua BioMedical, Inc. (“Alliqua”), on a pro rata basis to the holders of its common stock of all of the outstanding shares of its wholly-owned subsidiary AquaMed Technologies, Inc (“AquaMed” or “we,” “our” and “us”). We refer to the distribution as the “Distribution.” We expect that, immediately following the Distribution, pursuant to the Agreement and Plan of Merger dated as of November 27, 2018, as amended by Amendment No. 1 to Agreement and Plan of Merger, dated as of January 8, 2019 (the “Merger Agreement”), by and among AquaMed, AQ TOP, LLC (“Merger Sub”) and TO Pharmaceuticals LLC (“TOP”), TOP will merge with and into Merger Sub with TOP as the surviving entity (the “Merger”), and following the Merger, will become a wholly owned subsidiary of AquaMed, subject to the terms and conditions in the Merger Agreement.

Each share of Alliqua common stock outstanding as of 5:00 p.m., New York City time, on the record date for the Distribution, which we refer to as the “Record Date,” will entitle its holder to receive its pro rata portion of the AquaMed common stock. The distribution of shares will be made to a third-party distribution agent in book-entry form for the benefit of the holders of Alliqua common stock. Immediately following the Distribution, as consideration for the Merger, the current members of TOP and other third-party investors in AquaMed will receive approximately 90% of the total number of shares of AquaMed common stock outstanding immediately after the Merger and the Private Placement (as defined below) (on a fully diluted basis), before giving effect to any fees payable in equity to financial advisors or other intermediaries.

If you are a record holder of Alliqua common stock as of the close of business on which is the record date for the Distribution, you will be entitled to receive shares of AquaMed common stock for every one share of Alliqua common stock you hold on that date. Alliqua will distribute the shares of AquaMed common stock in book-entry form, which means that we will not issue physical stock certificates. As discussed under “The Transactions — When and How You Will Receive AquaMed Shares,” if you sell your Alliqua common stock in the “regular-way” market after the record date and before the Distribution, you also will be selling your right to receive shares of AquaMed common stock in connection with the Distribution. Immediately following the Distribution, AquaMed and TOP will consummate the Merger.

The Distribution will be effective by 11:59 p.m., New York City time, on , 2019. Immediately after the Distribution, AquaMed will be an independent company.

Alliqua’s stockholders are not required to vote on or take any other action in connection with the spin-off. We are not asking you for a proxy, and request that you do not send us a proxy. Alliqua stockholders will not be required to pay or otherwise provide any consideration for the shares of AquaMed common stock they receive in the spin-off, and they will not be required to surrender or exchange their shares of Alliqua common stock or take any other action in connection with the spin-off.

Alliqua currently owns all of the outstanding shares of AquaMed common stock. Accordingly, no trading market for AquaMed common stock currently exists. We expect trading of AquaMed common stock will begin on the first trading day after the Distribution Date. We intend to list AquaMed common stock on The Nasdaq Capital Market under the symbol “TOPP.”

In reviewing this prospectus, you should carefully consider the matters described in the section titled “Risk Factors” beginning on page 25 of this prospectus for a discussion of certain factors that should be considered by recipients of AquaMed common stock.

Neither the Securities and Exchange Commission nor any state securities commission has approved or disapproved of these securities or determined that this prospectus is truthful or complete. Any representation to the contrary is a criminal offense.

This prospectus does not constitute an offer to sell or the solicitation of an offer to buy any securities.

The date of this prospectus is , 2019.

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INDUSTRY AND MARKET DATA

Unless otherwise indicated, information contained in this prospectus concerning our industry and the markets in which we operate is based on information from independent industry and research organizations, other third-party sources and management estimates. Management estimates are derived from publicly available information released by independent industry analysts and third-party sources, as well as data from our internal research, and are based on assumptions made by us upon reviewing such data and our knowledge of such industry and markets, which we believe to be reasonable. Such data involve uncertainties and risk and are subject to change due to a variety of factors, including those described under “Risk Factors.”

BASIS OF PRESENTATION

For the presented periods through July 13, 2018, T.O. Global LLC, a New York limited liability company (“TOG”), was the beneficial owner of all of the outstanding membership interests of TOP. All financial statements and financial information and all information with respect to the business and operations of TOP and its respective subsidiaries for periods prior to the consummation of the Merger, including under “Summary Historical Consolidated Financial Data of TOP,” “Selected Historical Consolidated Financial Data for TOP,” “Business of TOP” and “Management’s Discussion and Analysis of Financial Condition and Plan of Operation of TOP” are presented on a consolidated basis for TOP and its respective subsidiaries, on a stand-alone basis from TOG. All references to “TOP” are to TO Pharmaceuticals LLC and its subsidiaries on a consolidated basis.

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INTRODUCTION

On November 28, 2018, Alliqua BioMedical, Inc. (“Alliqua”) announced plans to separate its custom hydrogel and contract manufacturing business from Alliqua and to combine such business with TO Pharmaceuticals LLC (“TOP”) and its subsidiaries pursuant to the Agreement and Plan of Merger (the “Merger Agreement”) dated as of November 27, 2018. Prior to the Merger, Alliqua will distribute all of the shares of AquaMed common stock on a pro rata basis to the record holders of Alliqua common stock (the “Distribution”). Prior to the Distribution, Alliqua is undertaking a series of internal transactions, following which AquaMed will own all of the assets and liabilities of the custom hydrogel and contract manufacturing business. We refer to this series of internal transactions as the “Internal Reorganization,” which is described in more detail under “The Asset Contribution and Separation Agreement and Ancillary Agreements.” We refer to the Internal Reorganization and the Distribution collectively as the “Spin-Off.”

In this prospectus, unless otherwise noted or the context otherwise requires:

•

“Alliqua” refers to Alliqua BioMedical, Inc. and its consolidated subsidiaries other than, for all periods following the Spin-Off, AquaMed and its consolidated subsidiaries;

•

“AquaMed”, “we”, “our” and “us” refers to AquaMed Technologies, Inc. and its consolidated subsidiaries, including, with respect to periods following the consummation of the Spin-Off and the Merger, TOP and its consolidated subsidiaries;

•

“Merger Sub” refers to AQ TOP, LLC, a wholly owned subsidiary of AquaMed; and

•

“TOP” refers to TO Pharmaceuticals LLC and its subsidiaries.

The Merger Agreement provides that, at closing, the following transactions will occur (in each case subject to the terms and conditions in the Merger Agreement): Merger Sub will merge with and into TOP (the “Merger”), with TOP surviving the Merger and becoming a wholly-owned subsidiary of AquaMed. Pursuant to and subject to the conditions in the Merger Agreement, the Merger will occur after the consummation by Alliqua of the Spin-Off. Following the Merger, AquaMed is expected to be renamed “TO Pharma Inc.,” and the pre-Merger shareholders of Alliqua will own approximately 10% of the issued and outstanding shares of AquaMed, before giving effect to any fees payable in equity to financial advisors or other intermediaries or any issuances in respect of the Private Placement or other concurrent financing transaction in respect of greater than $10 million of gross proceeds.

The consummation of the Merger is subject to, among other conditions:

•

AquaMed shall have received binding commitments from third-party investors to consummate an equity financing of AquaMed in a minimum aggregate amount of $10 million immediately prior to the effective time of the Merger, subject to waiver of such minimum amount by both parties (the “Private Placement”);

•

the Spin-Off having been consummated;

•

the effectiveness of the registration statement of which this prospectus forms a part in connection with the Distribution;

•

the approval for listing on the Nasdaq Capital Market of AquaMed common stock;

•

the board of directors of AquaMed shall have received an independent third-party valuation of the shares of AquaMed common stock to be distributed in the Distribution;

•

each of AquaMed and TOP shall have delivered audited financial statements to the other party;

•

the accuracy of the parties’ representations and warranties and the performance of their respective covenants contained in the Merger Agreement; and

•

certain other customary conditions.

The Merger Agreement contains customary representations, warranties and covenants, including a requirement to use reasonable best efforts to consummate the Private Placement and the Merger prior to April 11, 2019.

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SUMMARY

This summary highlights certain significant aspects of our business and is a summary of information contained elsewhere in this prospectus. This summary is not complete and you should carefully read this entire prospectus, including the information presented under the sections titled “Risk Factors,” “Cautionary Statement Concerning Forward-Looking Statements,” “Unaudited Pro Forma Condensed Combined Financial Statements of the Surviving Company,” “Selected Historical Financial Data of AquaMed,” “Selected Historical Consolidated Financial Data of TOP,” “Management’s Discussion and Analysis of Financial Condition and Results of Operations of AquaMed,” “Management’s Discussion and Analysis of Financial Condition and Plan of Operation of TOP,” and the financial statements and the related notes thereto included elsewhere in this prospectus. This summary contains forward-looking statements that involve risks and uncertainties. Our actual results may differ significantly from results contemplated in the forward-looking statements as a result of various factors such as those set forth in the sections titled “Risk Factors” and “Cautionary Statement Concerning Forward-Looking Statements.” When making an investment decision, you should also read the discussion under “Basis of Presentation,” and “Introduction” for the definition of some of the terms used in this prospectus and other matters described in this prospectus. As used in this prospectus, references to “pro forma” or “on a pro forma basis” mean giving pro forma effect to the Spin-Off and Merger as described in “Unaudited Pro Forma Condensed Combined Financial Statements of the Surviving Company.”

Overview

After completing the Spin-Off and the Merger, we will be an independent, publicly traded company dedicated to discovering, developing and commercializing novel therapeutics based on TOP’s proprietary cannabinoid product platform.

The Transactions

Overview

On November 28, 2018, Alliqua announced plans for the complete legal and structural separation of its custom hydrogel and contract manufacturing business and the combination of AquaMed’s business and the TOP businesses.

To effectuate the separation, Alliqua is undertaking the Internal Reorganization described under “The Asset Contribution and Separation Agreement and Ancillary Agreements.” After giving effect to the Internal Reorganization, we will hold all of the assets and liabilities related to the custom hydrogel and contract manufacturing business.

Following the Internal Reorganization, Alliqua will distribute all of its equity interest in us, consisting of all of the outstanding shares of our common stock, to the record holders of Alliqua common stock on a pro rata basis.

Following the Spin-Off, under the Merger Agreement and in accordance with Delaware law, Merger Sub will merge with and into TOP, with TOP surviving the Merger. As a result of the Merger, TOP will become a wholly owned subsidiary of AquaMed. For details of the structure of the transaction, see “The Merger Agreement.”

Transaction Rationale

The board of directors of Alliqua considered the following potential benefits in deciding to pursue the Spin-Off and Merger:

•

Stockholder Value. On October 11, 2018, Alliqua signed an Agreement and Plan of Merger and Reorganization (the “Adynxx Merger Agreement”) with Adynxx, Inc. (“Adynxx”) and Embark Merger Sub, Inc. (“Embark”), a wholly-owned subsidiary of Alliqua. Pursuant to the Adynxx Merger Agreement, Embark will merge with and into Adynxx, with Adynxx continuing as the surviving corporation, and the former Adynxx stockholders will own approximately 86% of Alliqua’s outstanding equity after the transaction (the “Adynxx Merger”). AquaMed’s custom

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hydrogels contract manufacturing business is not synergistic with the potential combined operations of Alliqua and Adynxx. In addition, under the terms of the Adynxx Merger Agreement, Alliqua is required to use its commercially reasonable efforts to spin-off AquaMed’s custom hydrogels business. We believe the Spin-Off and the Merger will provide greater value to Alliqua stockholders than if the AquaMed business remained a part of Alliqua following the closing of the Adynxx Merger as the combination of AquaMed and TOP will create an independent, publicly traded company dedicated to discovering, developing and commercializing novel therapeutics based on TOP’s proprietary cannabinoid-based product platform and serving customers in the cannabinoid pharmaceutical therapy industry.

•

Strategic Focus and Flexibility. Following the Spin-Off and Merger, we will be better able to dedicate financial and human capital resources to pursue appropriate growth opportunities and execute strategic plans best suited to our business than if we remained a part of Alliqua or as an independent company without the business combination with TOP.

•

Strategic Positioning in Industry. The combination of AquaMed and TOP is a strategic move to position the combined company as an independent, publicly traded cannabinoid pharmaceutical therapy-based company. The combination of AquaMed and TOP is expected to provide opportunities for the combined company to leverage its unique ability to create novel therapeutics based on TOP’s proprietary cannabinoid-based product platform in a number of U.S. Food and Drug Administration (the “FDA”)-regulated clinical indications, including a hydrogel product.

•

Management Incentives. The Spin-Off will enable AquaMed to create incentives for its management and employees that are more closely tied to its business performance and stockholder expectations. AquaMed’s equity-based compensation arrangements will more closely align the interests of AquaMed’s management and employees with the interests of its stockholders and should increase AquaMed’s ability to attract and retain personnel.

•

Capital Structure and Stockholder Flexibility. The segments in which Alliqua and AquaMed expect to operate have historically had different growth profiles and cash flow dynamics. The Spin-Off will allow Alliqua and AquaMed to separately manage their capital strategies and cost structures and will allow investors to make independent investment decisions with respect to Alliqua and AquaMed, including the ability for AquaMed to achieve alignment with a more natural stockholder base. Investment in one or the other company may appeal to investors with different goals, strategies, interests and concerns.

The Companies

AquaMed

We were incorporated in Delaware on January 13, 2009. We manufacture high water content, electron beam cross-linked, aqueous polymer hydrogels, or gels, used for wound care, medical diagnostics, transdermal drug delivery and cosmetics. We specialize in custom gels by capitalizing on proprietary manufacturing technologies. We have historically served as a contract manufacturer, supplying our gels to third parties who incorporate them into their own products. Our products are manufactured using proprietary and non-proprietary mixing, coating and cross-linking technologies. Together, these technologies enable us to produce gels that can satisfy rigid tolerance specifications with respect to a wide range of physical characteristics (e.g., thickness, water content, adherence, absorption, moisture vapor transmission rate (a measure of the passage of water vapor through a substance) and release rate) while maintaining product integrity. Additionally, we have the manufacturing ability to offer broad choices in the selection of liners onto which the gels are coated. Consequently, our customers are able to determine tolerances in moisture vapor transmission rate and active ingredient release rates while personalizing color and texture.

Our principal executive offices are located at 2150 Cabot Boulevard West, Suite B, Langhorne, PA 19047. Our telephone number is (215)-702-8550. Following the Spin-Off and the Merger, our website address will be www.topharm.com. Information contained on, or connected to, our website or Alliqua’s website does not and will not constitute part of this prospectus or the registration statement on Form S-1 of which this prospectus is a part.

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TOP

TOP was organized on October 21, 2015 in Delaware and is an early stage biopharmaceutical company engaged in the business of discovering, developing and commercializing drugs containing cannabinoids, which are based on a proprietary cannabinoid-based product platform, for the treatment of various diseases, disorders and medical conditions. TOP’s business is focused on research and development of potential pharmaceutical products based on compounds derived from the proprietary strains of Tikun Olam Ltd., a corporation formed pursuant to the laws of Israel (“TOL”). Through collaboration with TOL and leading medical experts at major Israeli hospitals and research organizations, TOP has initially focused its research and development efforts on Crohn’s Disease, ulcerative colitis, agitation in Alzheimer’s or other dementia, autism spectrum disorder, Tourette syndrome, acute migraines and dialysis.

TOP’s principal executive offices are located at 77 Water Street, 8th Floor, New York, New York 10005. TOP’s telephone number is (212) 837-8333.

Emerging Growth Company Status of AquaMed

Following the Spin-off, we will be an “emerging growth company” as defined in Jumpstart Our Business Startups Act of 2012 (the “JOBS Act”). As such, we will be eligible to take advantage of certain exemptions from various reporting requirements that apply to other public companies that are not emerging growth companies, including, compliance with the auditor attestation requirements of Section 404 of the Sarbanes-Oxley Act and the requirements to hold a non-binding advisory vote on executive compensation and any golden parachute payments not previously approved. We have not made a decision whether to take advantage of any or all of these exemptions. If we do take advantage of some or all of these exemptions, some investors may find our common stock less attractive. The result may be a less active trading market for our common stock and its stock price may be more volatile.

In addition, Section 107 of the JOBS Act provides that an emerging growth company may take advantage of the extended transition period provided in Section 13(a) of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), for complying with new or revised accounting standards, meaning that we, as an emerging growth company, can delay the adoption of certain accounting standards until those standards would otherwise apply to private companies. We have elected to take advantage of this extended transition period; however, it is our present intention to adopt any applicable accounting standards timely. If at some time we delay adoption of a new or revised accounting standard, our financial statements may not be comparable to those of companies that comply with such new or revised accounting standards. Section 107 of the JOBS Act provides that our decision not to opt out of the extended transition period for complying with new or revised accounting standards is irrevocable.

We may remain an emerging growth company until the earliest of (a) the last day of the first fiscal year in which our annual gross revenues exceed $1 billion, (b) the last day of the fiscal year following the fifth anniversary of the date of the first sale of our common equity securities pursuant to an effective registration statement under the Securities Act of 1933, as amended (the “Securities Act”), (c) the date we become a “large accelerated filer” as defined in Rule 12b-2 under the Exchange Act, which would occur if the market value of our common stock that is held by non-affiliates exceeds $700 million as of the last business day of its most recently completed second fiscal quarter, and (d) the date on which we have issued more than $1 billion in non-convertible debt during the preceding three-year period.

Questions and Answers about the Transactions

The following provides only a summary of the terms of the Spin-Off, the Merger and the transactions contemplated thereby. You should read the sections titled “The Transactions,” “The Merger Agreement” and “The Asset Contribution and Separation Agreement and Ancillary Agreements” below in this prospectus for a more detailed description of the matters described below.

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What is the Spin-Off?

The Spin-Off is the method by which we will separate from Alliqua. As part of the Spin-Off, Alliqua will undertake the Internal Reorganization so that we hold all assets and liabilities of its custom hydrogel and contract manufacturing business. Thereafter, in the Distribution, Alliqua will distribute to its stockholders all the outstanding shares of our common stock. Following the Spin-Off, we will be an independent, publicly-traded company, and Alliqua will not retain any ownership interest in us.

What is the Merger?

Under the terms of the Merger Agreement, after the Distribution, Merger Sub will merge with and into TOP, with TOP surviving the Merger. As a result of the Merger, TOP will become a wholly owned subsidiary of AquaMed. Immediately after the effective time of the Merger and consummation of the Private Placement, before giving effect to any fees payable in equity to financial advisors or other intermediaries, the current members of TOP and the third-party investors that participate in the Private Placement are expected to hold approximately 90% of the total number of shares of AquaMed common stock outstanding (on a fully diluted basis). Shares issued to Alliqua stockholders in the Distribution will constitute approximately 10% of the common stock of AquaMed outstanding after the effective time of the Merger and consummation of the Private Placement (on a fully diluted basis), assuming that no more than $10 million is raised in the Private Placement. Upon the consummation of the Merger, AquaMed is expected to be renamed “TO Pharma Inc.”

What is the Adynxx Merger?

Alliqua, Embark and Adynxx have entered into the Adynxx Merger Agreement, which contains the terms and conditions of the proposed business combination of Alliqua and Adynxx. Under the Adynxx Merger Agreement, Embark will merge with and into Adynxx, with Adynxx surviving as a wholly owned subsidiary of Alliqua. Immediately following the effective time of the Adynxx Merger, Adynxx equityholders will own approximately 86% of the combined company and Alliqua equityholders will own approximately 14% of the combined company, subject to certain adjustments. So long as Alliqua exercises commercially reasonable efforts to cause the Spin-Off to occur concurrently with the effective time of the Adynxx Merger, the occurrence of the Spin-Off is not a condition of Adynxx’s obligations to the consummate the transactions contemplated by the Adynxx Merger Agreement. The consummation of the Adynxx Merger, however, is a condition to the closing of the Spin-Off. In the event that Alliqua’s stockholders do not approve the Adynxx Merger and the Adynxx Merger is not consummated, then Alliqua may, in its discretion, determine not to effect the Spin-Off, in which case, we will remain a wholly-owned subsidiary of Alliqua.

Will the number of Alliqua shares I own change as a result of the Spin-Off and the Merger?

No, the number of shares of Alliqua common stock you own will not change as a result of the Spin-Off and the Merger.

What are the reasons for the Spin-Off and Merger?

The board of directors of Alliqua considered the following potential benefits in deciding to pursue the Spin-Off and Merger:

•

Stockholder Value. On October 11, 2018, Alliqua signed the Adynxx Merger Agreement with Adynxx and Embark, pursuant to which Alliqua will consummate the Adynxx Merger. AquaMed’s custom hydrogels contract manufacturing business is not synergistic with the potential combined operations of Alliqua and Adynxx. In addition, under the terms of the Adynxx Merger Agreement, Alliqua is required to use its commercially reasonable efforts to spin-off AquaMed’s custom hydrogels business. We believe the Spin-Off and the Merger will provide greater value to Alliqua stockholders than if the AquaMed business remained a part of Alliqua following the closing of the Adynxx Merger as the combination of AquaMed and TOP will create an

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independent, publicly traded company dedicated to discovering, developing and commercializing novel therapeutics based on TOP’s proprietary cannabinoid product platform and serving customers in the cannabinoid pharmaceutical therapy industry.

•

Strategic Focus and Flexibility. Following the Spin-Off and Merger, we will be better able to dedicate financial and human capital resources to pursue appropriate growth opportunities and execute strategic plans best suited to our business than if it remained a part of Alliqua or as an independent company without the business combination with TOP.

•

Strategic Positioning in Industry. The combination of AquaMed and TOP is a strategic move to position the combined company as an independent, publicly traded cannabinoid pharmaceutical therapy-based company. The combination of AquaMed and TOP is expected to provide opportunities for the combined company to leverage its unique ability to create novel therapeutics based on TOP’s proprietary cannabinoid product platform in a number of FDA-regulated clinical indications, including a hydrogel product.

•

Why is the separation of AquaMed structured as a Spin-Off?

Alliqua believes that a distribution of our shares is the most efficient way to separate our business from Alliqua in a manner that will achieve the benefits described above.

What will I receive in the Distribution?

As a holder of Alliqua common stock, you will receive a dividend of shares of our common stock for every one share of Alliqua common stock you hold on the Record Date (as defined below). The distribution agent will distribute only whole shares of our common stock in the Distribution. No fractional shares of our common stock will be issued pursuant to the dividend. Instead, any fractional shares of AquaMed common stock otherwise issuable to you will be sold on your behalf, and you will receive a cash payment with respect to that fractional share. Your proportionate interest in Alliqua will not change as a result of the Distribution. For a more detailed description, see “The Transactions.”

How will fractional shares be treated in the Spin-Off?

Any fractional shares of AquaMed common stock otherwise issuable to you will be sold on your behalf, and you will receive a cash payment with respect to that fractional share. The distribution agent will aggregate all fractional shares into whole shares and sell the whole shares in the open market at prevailing market prices on behalf of Alliqua stockholders entitled to receive a fractional share. The distribution agent will then distribute the aggregate cash proceeds of the sales, net of brokerage fees and other costs, pro rata to these holders (net of any required withholding for taxes applicable to each holder). For an explanation of how the cash payments for fractional shares will be determined, see “The Transactions — Treatment of Fractional Shares.”

What is being distributed in the Distribution?

Alliqua will distribute approximately 1,750,000 shares of our common stock in the Distribution, based on the approximately 5,005,210 shares of Alliqua common stock outstanding as of December 31,

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2018. The actual number of shares of our common stock that you will receive will depend on the actual number of shares of Alliqua common stock outstanding on the Record Date, which will reflect any issuance of new shares or exercises of outstanding options pursuant to Alliqua’a equity plans on or prior to the Record Date. The shares of our common stock that Alliqua distributes will constitute all of the issued and outstanding shares of our common stock immediately prior to the Distribution. For more information on the shares being distributed in the Spin-Off, see “Description of Our Capital Stock — Common Stock.”

Alliqua stockholders will not receive any new shares of common stock of AquaMed in the Merger and will continue to hold the AquaMed shares they received in the Distribution. The Merger will result in the current members of TOP and the third-party investors that participate in the Private Placement owning approximately 90% of the common stock of AquaMed outstanding immediately after the effective time of the Merger (on a fully diluted basis), before giving effect to any fees payable in equity to financial advisors or other intermediaries. Shares issued to Alliqua stockholders in the Distribution will constitute approximately 10% of the common stock of AquaMed outstanding after the effective time of the Merger (on a fully diluted basis), assuming that no more than $10 million is raised in the Private Placement.

What is the record date for the Distribution?

Alliqua will determine record ownership as of the close of business on , 2019 which we refer to as the “Record Date,” in order to determine the stockholders entitled to receive shares of AquaMed common stock in the Distribution.

When will the Distribution occur?

The Distribution will be effective by 11:59 p.m., New York City time, on , 2019, which we refer to as the “Distribution Date.” On or shortly after the Distribution Date, shares of our common stock will be credited in book-entry accounts for Alliqua stockholders entitled to receive the shares in the Distribution. See “How will Alliqua distribute shares of our common stock?” for more information on how to access your book-entry account or your bank, brokerage or other account holding the AquaMed common stock you receive in the Distribution on and following the Distribution Date.

What do I have to do to participate in the Distribution?

You are not required to take any action, but we urge you to read this prospectus carefully. Holders of Alliqua common stock will not need to pay any cash or provide any other consideration, including any shares of Alliqua common stock, in order to receive shares of our common stock in the Distribution. In addition, no stockholder approval of the Distribution is required. We are not asking you for a vote and request that you do not send us a proxy. Neither the Distribution nor the Merger will result in any changes in Alliqua stockholders’ ownership of Alliqua common stock. No vote of Alliqua stockholders is required or sought in connection with the Distribution or the Merger.

If I sell my shares of Alliqua common stock on or before the Distribution Date, will I still be entitled to receive shares of AquaMed common stock in the Distribution?

If you hold shares of Alliqua common stock on the Record Date and sell them on or before the Distribution Date in the “regular-way” market, you also will be selling your right to receive shares of AquaMed common stock in connection with the Distribution. If you wish to sell your Alliqua common stock with or without your entitlement to our common stock, you should discuss these alternatives with your bank, broker or other nominee. See “The Transactions — When and How You Will Receive AquaMed Shares” for more information.

What is “regular-way” and “ex dividend” trading of Alliqua common stock?

We anticipate that, on or shortly before the Record Date, there will be two markets in Alliqua common stock: (1) a “regular-way” market on which shares of Alliqua common stock will trade with the entitlement for the purchaser of Alliqua common stock to receive shares of our common stock to be

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distributed in the Distribution, and (2) an “ex dividend” market on which shares of Alliqua common stock will trade without the entitlement for the purchaser of Alliqua common stock to receive shares of our common stock. If you hold shares of Alliqua common stock on the Record Date and then sell those shares before the Distribution Date, you should make sure your stockbroker, bank or other nominee understands whether you want to sell your shares of Alliqua common stock with or without your entitlement to AquaMed common stock pursuant to the Distribution.

How will Alliqua distribute shares of our common stock?

Registered stockholders. If you own your shares of Alliqua common stock directly through Alliqua’s transfer agent, Action Stock Transfer Corporation, you are a registered stockholder. In this case, the distribution agent will credit the shares of our common stock you receive in the Distribution by way of direct registration in book-entry form to a new account with our transfer agent. Registration in book-entry form refers to a method of recording share ownership where no physical stock certificates are issued to stockholders, as is the case in the Distribution. You will be able to access information regarding your book-entry account holding the AquaMed shares at or by calling Action Stock Transfer Corporation at .

“Street name” or beneficial stockholders. If you own your shares of Alliqua common stock through a bank, broker or other nominee, your bank, broker or other nominee will credit your account with the shares of our common stock that you receive in the Distribution on or shortly after the Distribution Date. We encourage you to contact your bank, broker or other nominee if you have any questions concerning the mechanics of having shares held in “street name.”

We will not issue any physical stock certificates to any stockholders, even if requested. See “The Transactions — When and How You Will Receive AquaMed Shares” for a more detailed explanation.

What are the U.S. federal income tax consequences to me of the Distribution?

The receipt by you of shares of AquaMed common stock in the Spin-Off (including any fractional shares sold on your behalf) will generally be a taxable dividend to the extent of your ratable share of Alliqua’s current and accumulated earnings and profits, with the excess treated first as a non-taxable return of capital to the extent of your tax basis in shares of Alliqua’s common stock and then as capital gain. STOCKHOLDERS ARE ENCOURAGED TO CONSULT THEIR OWN TAX ADVISORS REGARDING THE PARTICULAR TAX CONSEQUENCES OF THE SPIN-OFF TO THEM, INCLUDING THE APPLICABILITY AND EFFECT OF ANY U.S. FEDERAL, STATE AND LOCAL TAX LAWS, AS WELL AS FOREIGN TAX LAWS.

How will I determine the tax basis I will have in the AquaMed shares I receive in the Spin-Off?

Your tax basis in the shares of AquaMed common stock received generally will equal the fair market value of such shares on the distribution date. For a more detailed discussion see “Material U.S. Federal Income Tax Consequences of the Distribution,” included elsewhere in this prospectus.

Does AquaMed intend to pay dividends?

We do not currently anticipate paying any dividends following the Spin-Off. The timing, declaration, amount and payment of any future dividends to our stockholders will fall within the discretion of our Board of Directors and will depend on many factors, including our financial condition, results of operations and capital requirements, legal requirements, regulatory constraints, industry practice and other business considerations that our Board of Directors deems relevant from time to time. In addition, the terms of the agreements governing our debt or debt that we may incur in the future may restrict the payments of dividends. See “Dividend Policy” for more information.

What are the financing plans for AquaMed, and what will be the indebtedness of AquaMed and its subsidiaries following the completion of the Transactions?

AquaMed’s intended financing in connection with the Spin-Off and Merger includes a minimum equity financing of $10 million. See “Management’s Discussion and Analysis of Financial Condition

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and Results of Operations of AquaMed — Liquidity and Capital Resources Following the Transactions” for more information. It is not anticipated that AquaMed will have any outstanding indebtedness following the consummation of the Distribution and Merger other than trade payables incurred in the ordinary course of business.

How will AquaMed common stock trade?

Currently, there is no public market for our common stock. We intend to list our common stock on the Nasdaq Capital Market under the symbol “TOPP.”

What will be the relationship between Alliqua and AquaMed following the Distribution?

Following the Distribution, Alliqua will not own any of our shares and we will operate independently of Alliqua. Apart from our Chairman, who will remain a director of Alliqua after the Distribution and the Adynxx Merger, we currently do not expect other members of our Board of Directors to be officers or directors of Alliqua. In addition, we do not expect to depend on Alliqua to conduct our business following the Distribution apart from certain limited transitional support services. In order to govern the ongoing relationships between us and Alliqua after the Spin-Off and to facilitate an orderly transition, we and Alliqua intend to enter into agreements providing for various services and rights following the Spin-Off and under which we and Alliqua will agree to indemnify each other against certain liabilities arising from our respective businesses. These agreements will, among other things, provide arrangements for employee and pension-related matters, tax matters, intellectual property matters as well as transitional services and non-U.S. agency services. See “Risk Factors — Risks Relating to the Spin-Off and the Merger,” “The Asset Contribution and Separation Agreement and Ancillary Agreements” and “Certain Relationships and Related Party Transactions — Agreements with Alliqua” for details.

Will the Spin-Off affect the trading price of my Alliqua common stock?

Yes. We expect the trading price of shares of Alliqua common stock immediately following the Distribution to be lower than the “regular-way” trading price of such shares immediately prior to the Distribution because the trading price will no longer reflect the value of the AquaMed business. Furthermore, until the market has fully analyzed the value of Alliqua without the AquaMed business, the trading price of shares of Alliqua common stock may fluctuate. There can be no assurance that, following the Distribution, the combined trading prices of Alliqua common stock and our common stock will equal or exceed what the trading price of Alliqua common stock would have been in the absence of the Spin-Off.

It is possible that after the Spin-Off, the combined market value of the equity of Alliqua and AquaMed will be less than Alliqua’s equity value before the Spin-Off.

Do I have appraisal rights in connection with the Spin-Off?

No. Holders of Alliqua’s common stock are not entitled to appraisal rights in connection with the Spin-Off.

Are there risks associated with owning shares of AquaMed’s common stock?

Yes. Our business faces both general and specific risks and uncertainties relating to the AquaMed business and the TOP business. Our business also faces risks relating to the Spin-Off and Merger. Following the Spin-Off, we will also face risks associated with being an independent, publicly-traded company. Accordingly, you should read carefully the information set forth in the section titled “Risk Factors” in this prospectus.

Who is the distribution agent, transfer agent and registrar for AquaMed common stock?

Action Stock Transfer Corporation.

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Summary of the Spin-Off

Distributing Company

Alliqua BioMedical, Inc., a Delaware corporation that holds all of our common stock issued and outstanding prior to the Distribution. After the Distribution, Alliqua will not own any shares of our common stock.

Distributed Company

AquaMed Technologies, Inc., a Delaware corporation and a wholly owned subsidiary of Alliqua. At the time of the Distribution, we will hold assets and liabilities relating to Alliqua’s custom hydrogels manufacturing business. After the Spin-Off, we will be an independent publicly-traded company.

Distributed Securities

100% of our common stock issued and outstanding immediately prior to the Distribution. Based on the approximately 5,005,210 shares of Alliqua common stock outstanding on December 31, 2018, and applying the distribution ratio of shares of AquaMed common stock for every one share of Alliqua common stock, approximately 1,750,000 shares of AquaMed common stock will be distributed in the Spin-Off. The actual number of shares of our common stock you will receive in the Spin-Off will depend on the actual number of shares of Alliqua common stock outstanding on the Record Date, which will reflect any issuance of new shares or exercises of outstanding options pursuant to Alliqua equity plans on or prior to the Record Date.

Record Date

The Record Date is the close of business on , 2019.

Distribution Date

The Distribution Date is , 2019.

Internal Reorganization

In connection with the Spin-Off, Alliqua will undertake the Internal Reorganization so that we hold all of the assets relating to the custom hydrogel and contract manufacturing business. See “The Asset Contribution and Separation Agreement and Ancillary Agreements” for a description of the Internal Reorganization.

Distribution Ratio

Each holder of Alliqua common stock will receive a dividend of shares of our common stock for every one share of Alliqua common stock it holds on the Record Date. The distribution agent will distribute only whole shares of our common stock in the Spin-Off. No fractional shares of our common stock will be issued pursuant to this dividend. Any fractional shares of AquaMed common stock otherwise issuable to you will be sold on your behalf, and you will receive a cash payment with respect to that fractional share. The distribution agent will aggregate all fractional shares into whole shares and sell the whole shares in the open market at prevailing market prices on behalf of Alliqua stockholders entitled to receive a fractional share. The distribution agent will then distribute the aggregate cash proceeds of the sales, net of brokerage fees and other costs, pro rata to these holders (net of any required withholding for taxes applicable to each holder).

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For an explanation of how the cash payments for fractional shares will be determined, see “The Transactions — Treatment of Fractional Shares.”

Please note that if you sell your shares of Alliqua common stock on or before the Distribution Date in the “regular-way” market, the buyer of those shares may in some circumstances be entitled to receive the shares of our common stock to be distributed in respect of the Alliqua shares that you sold. See “The Transactions — When and How You Will Receive AquaMed Shares” for more detail.

The Distribution

On the Distribution Date, Alliqua will release the shares of our common stock to the distribution agent to distribute to Alliqua stockholders. Alliqua will distribute our shares in book-entry form and thus we will not issue any physical stock certificates. We expect that it will take the distribution agent up to two weeks to electronically issue shares of our common stock to you or your bank or brokerage firm on your behalf by way of direct registration in book-entry form. The ability to trade our shares will not be affected during that time. You will not be required to make any payment, surrender or exchange your shares of Alliqua common stock or take any other action to receive your shares of our common stock, however, you generally will be treated as if you received a taxable distribution in an amount equal to the fair market value of AquaMed common stock received (including any fractional share deemed to be received by and sold on your behalf). See “Material U.S. Federal Income Tax Consequences of the Distribution” for more information.

We urge you to consult your tax advisor as to the specific tax consequences of the Distribution to you, including the effect of any U.S. federal, state, local or foreign tax laws and of changes in applicable tax laws.

Concurrent Private Placement

AquaMed’s contemplated financing in connection with the Spin-Off and Merger includes an equity financing in the minimum aggregate amount of $10 million; provided, that the parties may determine to waive the $10 million minimum. See “Management’s Discussion and Analysis of Financial Condition and Results of Operations of AquaMed — Liquidity and Capital Resources Following the Transactions” for more information.

Conditions to the Spin-Off

The Spin-Off is subject to the satisfaction, or the waiver of Alliqua’s board of directors, of the following conditions, among other conditions:

•

the board of directors of Alliqua shall have approved the Internal Reorganization and the Distribution and shall have declared the Distribution of AquaMed common stock to Alliqua stockholders;

•

the ancillary agreements contemplated by the Asset Contribution and Separation Agreement shall have been executed by each party to those agreements;

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•

the Securities and Exchange Commission (“SEC”) shall have declared effective our Registration Statement on Form S-1, of which this prospectus is a part, under the Exchange Act, and no stop order suspending the effectiveness of the Registration Statement shall be in effect and no proceedings for that purpose shall be pending before or threatened by the SEC;

•

our common stock shall have been accepted for listing on the Nasdaq Capital Market, subject to official notice of issuance;

•

we shall have concurrently consummated the Private Placement;

•

the Merger Agreement shall be in full force and effect;

•

Alliqua shall have received an independent third-party valuation of our common stock to be distributed in the Distribution;

•

no order, injunction or decree issued by any governmental authority of competent jurisdiction or other legal restraint or prohibition preventing consummation of the Internal Reorganization shall be in effect;

•

Alliqua shall be satisfied the Internal Reorganization and the Distribution will not result in any material tax payable by Alliqua;

•

the Adynxx Merger Agreement between Alliqua, Embark and Adynxx dated October 11, 2018, shall be in full force and effect and the transactions contemplated thereby shall be consummated immediately following the closing of the Spin-Off; and

•

no proceeding shall be pending or threatened in writing seeking to enjoin, delay, prohibit or restrict the consummation of the Spin-Off or the Merger.

Regulatory Approvals

We are not aware of any material federal, foreign or state regulatory requirements with which we must comply, other than SEC rules and regulations, or any material approvals that we must obtain, other than the approval for listing of our common stock by the Nasdaq Capital Market and the SEC’s declaration of the effectiveness of the Registration Statement, which are conditions to the Distribution and the Merger.

Trading Market and Symbol

We intend to file an application to list our common stock on the Nasdaq Capital Market under the symbol “TOPP.” We anticipate that trading of our common stock will begin the first trading day after the Distribution Date.

We anticipate that, beginning on or shortly before the Record Date, there will be two markets in Alliqua common stock: (1) a “regular-way” market on which shares of Alliqua common stock will trade with the entitlement for

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the purchaser of Alliqua common stock to receive shares of our common stock to be distributed in the Distribution, and (2) an “ex-dividend” market on which shares of Alliqua common stock will trade without the entitlement for the purchaser of Alliqua common stock to receive shares of our common stock. If you hold shares of Alliqua common stock on the Record Date and then decide to sell any shares of Alliqua common stock before the Distribution Date, you should make sure your stockbroker, bank or other nominee understands whether you want to sell your shares of Alliqua common stock with or without your entitlement to AquaMed common stock pursuant to the Distribution.

Tax Consequences to Alliqua Stockholders

For U.S. federal income tax purposes, the Distribution by Alliqua of the shares of AquaMed common stock will not be eligible for treatment as a tax-free distribution. Accordingly, each holder of Alliqua common stock who receives shares of AquaMed common stock in the Spin-Off generally will be treated as if such stockholder received a taxable distribution in an amount equal to the fair market value of AquaMed common stock received (including any fractional share deemed to be received by and sold on behalf of the stockholder), which will result in: (a) a dividend to the extent of such stockholder’s ratable share of Alliqua’s current and accumulated earnings and profits; then (b) a reduction in such stockholder’s basis in Alliqua’s common stock (but not below zero) to the extent the amount received exceeds the amount referenced in clause (a); and then (c) gain from the sale or exchange of Alliqua common stock to the extent the amount received exceeds the sum of the amounts referenced in clauses (a) and (b). Each stockholder’s basis in his, her or its AquaMed common stock will be equal to the fair market value of such stock at the time of the Spin-Off. A stockholder’s holding period for such shares will begin the day after the Spin-Off date.

Relationship with Alliqua after the Spin-Off

Following the Distribution, Alliqua will not own any of our shares and we will operate independently of Alliqua. In addition, we do not expect to depend on Alliqua to conduct our business following the Distribution apart from certain limited transitional support services. In order to govern the ongoing relationships between us and Alliqua after the Spin-Off and to facilitate an orderly transition, we and Alliqua intend to enter into agreements providing for various services and rights following the Spin-Off and

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under which we and Alliqua will agree to indemnify each other against certain liabilities arising from our respective businesses. These agreements include:

•

the Asset Contribution and Separation Agreement that will set forth Alliqua’s and our agreements regarding the principal actions that both parties will take in connection with the Spin-Off, including the assignment by Alliqua to us of the assets relating to our hydrogel business which we do not already own, and aspects of our relationship following the Spin-Off;

•

a Tax Matters Agreement that will govern the respective rights, responsibilities and obligations of Alliqua and us after the Spin-Off with respect to all tax matters;

•

A Bill of Sale and Assignment and Assumption Agreement (the “Assumption Agreement”) whereby we will assume Alliqua’s liabilities related to the hydrogel business.

We describe these arrangements in greater detail under “The Asset Contribution and Separation Agreement and Ancillary Agreements” and “Certain Relationships and Related Party Transactions — Agreements with Alliqua,” and describe some of the risks of these arrangements under “Risk Factors — Risks Relating to the Spin-Off and the Merger.”

Dividend Policy

We do not anticipate paying cash dividends following the Spin-Off. The timing, declaration, amount and payment of any future dividends to our stockholders will fall within the discretion of our Board of Directors and will depend on many factors, including our financial condition, results of operations and capital requirements, legal requirements, regulatory constraints, industry practice and other business considerations that our Board of Directors deems relevant from time to time. In addition, the terms of agreements governing any debt that we may incur in the future may restrict or limit the payments of dividends. See “Dividend Policy.”

Transfer Agent

Action Stock Transfer Corporation

Risk Factors

We face both general and specific risks and uncertainties relating to the AquaMed business and the TOP business. We also face risks relating to the Spin-Off and Merger. Following the Spin-Off, we will also face risks associated with being an independent, publicly-traded company. Accordingly, you should read carefully the information set forth under “Risk Factors.”

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Summary of the Merger

Structure of the Merger

Under the Merger Agreement and in accordance with Delaware law, Merger Sub will merge with and into TOP, with TOP surviving the Merger. As a result of the Merger, TOP will become a wholly owned subsidiary of AquaMed. For details of the structure of the transaction, see “The Merger Agreement.”

Consideration for the Merger

At the effective time of the Merger, all of the outstanding membership interests of TOP will be automatically converted into the right to receive, in the aggregate, merger consideration consisting of shares of AquaMed common stock. Immediately after the effective time of the Merger and consummation of the Private Placement, before giving effect to any fees payable in equity to financial advisors or other intermediaries, the current members of TOP and the third-party investors that participate in the Private Placement are expected to hold approximately 90% of the total number of shares of AquaMed common stock outstanding (on a fully diluted basis) (the “Merger Consideration”).

Following the effective time of the Merger, all of the TOP membership interests will be automatically cancelled and cease to exist.

Approval of the Merger

No vote by Alliqua stockholders is required or is being sought in connection with the Merger. Alliqua, as the sole stockholder of AquaMed, has already approved the Merger. The board of managers of TOP has approved the Merger Agreement, the Merger and all other actions necessary to consummate the Merger. A majority of the members of TOP have also approved the Merger Agreement, the Merger and all other actions necessary to consummate the Merger.

Regulatory Approvals

We are not aware of any material federal, foreign or state regulatory requirements with which we must comply, other than SEC rules and regulations, or any material approvals that we must obtain, other than the approval for listing of our common stock and the SEC’s declaration of the effectiveness of the Registration Statement, which are conditions to the Distribution and the Merger.

Conditions to the Merger

The obligations of each party to consummate the Merger are subject to the satisfaction or waiver (to the extent permitted by applicable law) of closing conditions that are contained in the Merger Agreement, including:

•

the Spin-Off having occurred pursuant to the Asset Contribution and Separation Agreement;

•

the effectiveness of the registration statement of which this prospectus forms a part in connection with the Distribution, and the approval for listing on the Nasdaq Capital Market of the shares of AquaMed common stock to be issued in the Distribution and the Merger, subject to official notice of issuance;

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•

the absence of any order issued by any governmental authority of competent jurisdiction or other legal impediment preventing or making illegal the consummation of the Merger; and

•

we shall have received binding commitments from investors to consummate the Private Placement.

In addition, our, and Merger Sub’s obligations to consummate the Merger are subject to the satisfaction or waiver (to the extent permitted by applicable law) of the following conditions, among others:

•

certain fundamental representations and warranties of TOP being true and correct in all respects in each case as of the date of the Merger Agreement and as of the closing date of the Merger as if made as of the closing date of the Merger;

•

the representations and warranties of TOP, disregarding all materiality or material adverse effect qualifications, being true and correct in all respects in each case as of the date of the Merger Agreement and as of the closing date of the Merger as if made as of the closing date of the Merger (except to the extent such representations and warranties address matters as of a particular date, in which case as of such date) (other than the certain fundamental representations and warranties which must be true and correct in all respects);

•

the covenants and agreements being performed by TOP in all material respects at or prior to the effective time of the Merger;

•

TOP shall have obtained the consent of the holders of a majority of its membership interests, and such consent shall not have been invalidated or revoked and shall remain in full force and effect;

•

the absence of a TOP Material Adverse Effect since the date of the Merger Agreement;

•

TOP shall have completed an audit of its financial statements for the years ended December 31, 2016 and December 31, 2017 by an independent registered auditor; and

•

we shall have received an independent third-party valuation of our common stock to be distributed in the Distribution.

Furthermore, the obligations of TOP to consummate the Merger are subject to the satisfaction or waiver (to the extent permitted by applicable law) of the following conditions, among others:

•

certain fundamental representations and warranties of AquaMed and Merger Sub being true and correct in

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all respects in each case as of the date of the Merger Agreement and as of the closing date of the Merger as if made as of the closing date of the Merger;

•

the representations and warranties of AquaMed and Merger Sub, disregarding all materiality or material adverse effect qualifications, being true and correct in all respects in each case as of the date of the Merger Agreement and as of the closing date of the Merger as if made as of the closing date of the Merger (except to the extent such representations and warranties address matters as of a particular date, in which case as of such date) (other than the certain fundamental representations and warranties which must be true and correct in all respects);

•

the covenants and agreements being performed by AquaMed and Merger Sub in all material respects at or prior to the effective time of the Merger;

•

the absence of any AquaMed Material Adverse Effect since the date of the Merger Agreement;

•

AquaMed shall have completed an audit of its financial statements for the years ended December 31, 2016 and December 31, 2017 by an independent registered auditor; and

•

we shall have delivered to TOP (a) resignation letters of any of our officers and directors, to be effective as of the time when the Merger shall become effective (the “Effective Time”), who will not be continuing officers or directors of us, and (b) certified resolutions of our Board of Directors (i) causing our whole Board of Directors to consist of five directors as of the Effective Time, (ii) appointing to the Board of Directors such individuals as necessary to cause the Board of Directors as of the Effective Time to conform with the requirements set forth on Schedule 1.4 to the Merger Agreement, and (iii) appointing as officers of Parent such individuals as necessary to cause our officers as of the Effective Time to conform with the requirements set forth on Schedule 1.4 to the Merger Agreement. We shall also deliver resolutions, in our capacity as the sole member of the surviving company as of the Effective Time, appointing persons to the Board of Managers of the surviving company, and resolutions of such Board of Managers appointing persons to serve as officers of the surviving company.

To the extent permitted by applicable law, each party to the Merger Agreement may waive, at its sole discretion, any of the conditions to its respective obligations to complete the Merger.

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Termination of the Merger Agreement

The Merger Agreement may be terminated at any time before the effective time of the Merger by the mutual written consent of AquaMed and TOP. It may also be terminated by either us or TOP if:

•

the effective time of the Merger has not occurred on or before April 11, 2019 unless the failure to effect the Merger by that date is due to the failure of the party seeking to terminate the Merger Agreement to perform its obligations set forth in the Merger Agreement;

•

if a court of competent jurisdiction or other governmental authority shall have issued a final and non-appealable order, or shall have taken any other action, having the effect of permanently restraining, enjoining or otherwise prohibiting the Merger.

The Merger Agreement may also be terminated by:

•

TOP at any time before the effective time of the Merger if any of AquaMed’s representations and warranties shall be inaccurate such that the closing condition set forth above shall not be satisfied or any of AquaMed’s covenants or obligations shall have been materially breached, and such breach or inaccuracy has not been cured within 30 business days following notice of such inaccuracy or breach.

•

AquaMed at any time before the effective time of the Merger if any of TOP’s representations and warranties shall be inaccurate such that the closing condition set forth above shall not be satisfied or any of TOP’s covenants or obligations shall have been materially breached, and such breach or inaccuracy has not been cured within 30 business days following notice of such inaccuracy or breach.

Accounting Treatment of the Merger

The combined financial information presented in the prospectus was prepared using the purchase method of accounting, with TOP treated as the “acquirer” of AquaMed and its respective subsidiaries for accounting purposes.

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SUMMARY HISTORICAL FINANCIAL DATA OF AQUAMED

The following tables summarize the historical financial and other data of AquaMed for the periods and as of the dates indicated.

This summary historical financial data for the years ended December 31, 2017 and 2016, and as of December 31, 2017 and 2016, were derived from AquaMed’s audited financial statements and notes thereto included elsewhere in this prospectus. The summary historical financial data for the nine months ended September 30, 2018 and 2017, and as of September 30, 2018, were derived from AquaMed’s unaudited interim financial statements and notes thereto included elsewhere in this prospectus. These unaudited interim financial statements were prepared on a basis consistent with our audited financial statements and, in the opinion of AquaMed’s management, reflect all adjustments, consisting only of normal and recurring adjustments, necessary for a fair statement of the financial information.

Historical results are not necessarily indicative of future operating results, and the results for any interim period are not necessarily indicative of the results that may be expected for a full fiscal year. Because the data in this table is only a summary and does not provide all of the data contained in our combined financial statements, the information should be read in conjunction with “Selected Historical Financial Data of AquaMed,” “Management’s Discussion and Analysis of Financial Condition and Results of Operations of AquaMed” and its combined financial statements and the related notes thereto included elsewhere in this prospectus.

	As of or for the years ended						As of or for the nine months ended
	December 31, 2017			December 31, 2016			September 30, 2018			September 30, 2017
(in millions)	Historical						Historical (Unaudited)
Combined Statement of Operations data:
Revenue		$	1,992		$	2,152		$	1,752		$	1,330
Loss from operations before tax			(969)			(1,839)			(1,323)			(771)
Net loss			(953)			(1,776)			(1,323)			(759)
Combined Balance Sheet Data:
Total assets		$	894		$	1,261		$	1,153
Total current liabilities			210			384			561
Other long-term liabilities			59			83			53
Total liabilities			269			467			614
Combined Statements of Cash Flows data:
Cash flows (used in) operating activities		$	(777)		$	(1,317)		$	(1,237)		$	(847)
Cash flows (used in) investing activities			(7)			—			—			(7)
Cash flows provided by financing activities			784			1,317			1,237			854
Advances from Parent			784			1,317			1,237			854

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SUMMARY HISTORICAL CONSOLIDATED FINANCIAL DATA OF TOP

The following tables summarize the historical consolidated financial and other data of TOP for the periods and as of the dates indicated.

This summary historical consolidated financial data for the years ended December 31, 2017 and 2016, and as of December 31, 2017 and 2016, were derived from TOP’s audited consolidated financial statements and notes thereto included elsewhere in this prospectus. The summary historical consolidated financial data for the nine months ended September 30, 2018 and 2017, and as of September 30, 2018, were derived from TOP’s unaudited condensed consolidated interim financial statements and notes thereto included elsewhere in this prospectus. These unaudited condensed consolidated interim financial statements were prepared on a basis consistent with TOP’s audited consolidated financial statements and, in the opinion of TOP’s management, reflect all adjustments, consisting only of normal and recurring adjustments, necessary for a fair statement of the financial information.

Historical results are not necessarily indicative of future operating results, and the results for any interim period are not necessarily indicative of the results that may be expected for a full fiscal year. Because the data in this table is only a summary and does not provide all of the data contained in TOP’s consolidated financial statements, the information should be read in conjunction with “Selected Historical Consolidated Financial Data for TOP,” “Management’s Discussion and Analysis of Financial Condition and Plan of Operation of TOP” and its consolidated financial statements and the related notes thereto included elsewhere in this prospectus.

	As of or for the years ended						As of or for the nine months ended
	December 31, 2017			December 31, 2016			September 30, 2018			September 30, 2017
	Historical						Historical (Unaudited)
Consolidated Statement of Operations data:
Operating Expenses		$	737,670		$	1,060,395		$	636,888		$	524,758
Net loss			(737,670)			(1,060,395)			(636,888)			(524,758)
Consolidated Balance Sheet Data:
Total assets		$	471,500		$	479,750			529,063		$
Total current liabilities			2,269,465			1,540,045			2,963,916
Total liabilities			2,269,465			1,540,045			2,963,916
Members’ deficit		$	(1,797,965)		$	(1,060,295)		$	(2,434,853)
Consolidated Statements of Cash Flows data:
Cash flows (used in) operating activities		$	(625,393)		$	(1,024,017)		$	(404,626)		$	(456,640)
Cash flows provided by financing activities			625,393			1,024,017			404,626			456,640
Advances from TOG			625,393			1,024,017			404,626			456,640

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SUMMARY PRO FORMA CONDENSED COMBINED FINANCIAL DATA OF
THE SURVIVING COMPANY

The following tables summarize our pro forma condensed combined financial data for the periods and as of the dates indicated.

We have derived the summary pro forma condensed combined financial and other data for the periods and as of the dates indicated from our pro forma condensed combined financial statements and the notes thereto included elsewhere in this Prospectus.

Our pro forma condensed combined financial data are not necessarily indicative of the results we would have realized had the Spin-Off and the Merger been consummated on those dates, or of future operating results, and the results for any interim period are not necessarily indicative of the results that may be expected for a full fiscal year. Because the data in this table is only a summary and does not provide all of the data contained in our pro forma condensed combined financial statements, the information should be read in conjunction with our pro forma condensed combined financial statements and the related notes thereto included elsewhere in this Prospectus.

The following unaudited summary pro forma condensed combined financial information present the pro forma financial information of the surviving company based upon the historical financial statements of each of TOP and AqauMed, after giving effect to the Spin-off and Merger as further described in the section of this document entitled “The Transactions.” The unaudited summary condensed combined pro forma financial information are intended to reflect the impact of the Spin-Off and the Merger on AquaMed’s historical financial statements as if the relevant transactions occurred on September 30, 2018 for purposes of the unaudited pro forma condensed combined balance sheet and January 1, 2017 for purposes of the unaudited pro forma condensed combined statements of operations data. The unaudited pro forma condensed combined financial information and other data of the surviving company have been prepared using, and should be read in conjunction with (i) TOP’s audited historical consolidated financial statements and related notes for the year ended December 31, 2017, (ii) TOP’s unaudited historical consolidated financial statements and related notes as of and for the nine months ended September 30, 2018, (iii) AquaMed’s audited historical combined financial statements and related notes for the year ended December 31, 2017, and (iv) AquaMed’s unaudited historical combined financial statements and related notes as of and for the nine months ended September 30, 2018. The unaudited pro forma condensed combined financial information is presented for informational purposes only and is not intended to represent or to be indicative of the actual results of operations or financial position that the combined company would have reported had the Spin-Off and Merger been completed as of the dates set forth in the pro forma condensed combined financial statements, and should not be taken as being indicative of the combined company’s future consolidated results of operations or financial position. The actual results may differ significantly from those reflected in the pro forma condensed combined financial statements for a number of reasons, including differences between the assumptions used to prepare the pro forma condensed combined financial statements and actual amounts. This information is only a summary and has been derived from and should be read in conjunction with the more detailed unaudited pro forma condensed combined financial statements and the notes thereto, included elsewhere in this prospectus, which have been prepared in accordance with Article 11 of Regulation S-X.

(in thousands)	Historical TOP as of and for the Nine Months Ended September 30, 2018			Historical AquaMed as of and for the Nine Months Ended September 30, 2018			Transaction Adjustments			Pro Forma Combined
Revenue		$	—		$	1,752		$	—		$	1,752
Loss before income taxes			(637)			(1,323)			—			(1,960)
Income tax provision			—			—			—			—
Net loss		$	(637)		$	(1,323)		$	—		$	(1,960)
Total assets		$	530		$	1,153		$	—		$	1,683
Total liabilities		$	2,965		$	614		$	—		$	3,579

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RISK FACTORS

You should carefully consider all of the information in this prospectus and each of the risks described below, which we believe are the principal risks that we face. Some of the risks relate to the businesses of AquaMed and TOP, others to the Spin-Off, and others to the Merger. Some risks relate principally to the securities markets and ownership of our common stock.

Any of the following risks could materially and adversely affect our business, financial condition, results of operations and prospects and the actual outcome of matters as to which forward-looking statements are made in this prospectus. In such case, the trading price of our common stock could decline, and you could lose all or part of your investment. While we believe we have identified and discussed below the material risks affecting our business, there may be additional risks and uncertainties that we do not presently know or that we do not currently believe to be material that may adversely affect our business, financial condition, results of operations and prospects in the future.

Past performance may not be a reliable indicator of future financial performance. Future performance and historical trends may be adversely affected by the following factors, as well as other variables, and should not be relied upon to project future period results.

Risks Relating to AquaMed’s Business

The report of our independent registered public accounting firm contains an explanatory paragraph as to our ability to continue as a going concern, which could prevent us from obtaining new financing on reasonable terms or at all.

Because we have had recurring losses, negative cash flows from operating activities, and no cash on hand, the report of our independent registered public accounting firm, with respect to our financial statements at December 31, 2017, and for the year ended December 31, 2017, contains an explanatory paragraph as to our potential inability to continue as a going concern. This opinion indicates that substantial doubt exists regarding our ability to remain in business. Such an opinion may adversely affect our ability to obtain new financing on reasonable terms or at all.

Our future success depends upon market acceptance of our existing and future products.

We believe that our success will depend in part upon the acceptance of its existing and future products by the medical community, hospitals and physicians and other health care providers, third-party payers, and end-users. Such acceptance may depend upon the extent to which the medical community and end-users perceive our products as safer, more effective or cost-competitive than other similar products. Ultimately, for our products to gain general market acceptance, it may also be necessary for us to develop marketing partners for the distribution of our products. There can be no assurance that our products will achieve significant market acceptance on a timely basis, or at all. Failure of some or all of our future products to achieve significant market acceptance could have a material adverse effect on our business, financial condition, and results of operations.

We are dependent on significant customers.

Our hydrogel manufacturing business is currently our sole source of revenue, and much of this revenue is generated from a limited number of clients, who account for a substantial percentage of our total revenues. For the nine-month period ended September 30, 2018, two major customers accounted for approximately 75.4% of our revenue, with each customer individually accounting for 62.5%, and 12.9%, respectively. The loss of any of our significant customers would have a significantly negative effect on our overall operations.

We operate in a highly competitive industry.

Competition from other hydrogel manufacturers is intense. There can be no assurance that we can develop products that are more effective or achieve greater market acceptance than competitive products, or that our competitors will not succeed in developing or acquiring products and technologies that are more effective than those being developed by us, that would render our products and technologies less competitive or obsolete.

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Our competitors enjoy several competitive advantages over us, including some or all of the following:

•

large and established distribution networks in the U.S. and/or in international markets;

•

greater financial, managerial and other resources for products research and development, sales and marketing efforts and protecting and enforcing intellectual property rights;

•

significantly greater name recognition;

•

more expansive portfolios of intellectual property rights; and

•

greater experience in obtaining and maintaining regulatory approvals and/or clearances from the FDA and other regulatory agencies.

Our competitors’ products will compete directly with our products. In addition, our competitors, as well as new market entrants, may develop or acquire new products that will compete directly or indirectly with our products. The presence of this competition in our market may lead to pricing pressure which would make it more difficult to sell our products at a price that will make us profitable or prevent us from selling our products at all. Our failure to compete effectively would have a material and adverse effect on our business, results of operations and financial condition.

We are subject to governmental regulations.

As a manufacturer of medical products, we are generally subject to regulation by the FDA and the Federal Trade Commission, among other state and federal governmental authorities in the U.S., with respect to the manufacturing, marketing, labeling, record keeping, claims and advertising of our products. Our hydrogel manufacturing facility is also subject to various state regulations.

Failure to comply with applicable regulatory requirements can result in, among other things, suspensions or withdrawals of approvals or clearances, seizures or recalls of products, injunctions against the manufacture, holding, distribution, marketing and sale of a product, civil and criminal sanctions. Furthermore, changes in existing regulations or the adoption of new regulations could prevent us from obtaining, or affect the timing of, future regulatory approvals. Meeting regulatory requirements and evolving government standards may delay marketing of our products for a considerable period of time, impose costly procedures upon our activities and result in a competitive advantage to larger companies that compete against us.

We have limited sales, marketing and distribution capabilities.

We currently have limited sales, marketing and distribution capabilities. We must either develop our own sales, marketing and distribution capabilities, which will be expensive and time consuming, or make arrangements with third parties to perform these services for us. If we enter into third party arrangements, the third parties may not be capable of successfully selling any of our products. If we decide to market any of our products on our own, we will have to commit significant resources to developing a marketing and sales force and supporting distribution capabilities. If we decide to enter into arrangements with third parties for performance of these services, we may find that they are not available on terms acceptable to us, or at all. If we are not able to establish and maintain successful arrangements with third parties or build our own sales and marketing infrastructure, our business and financial condition will be adversely affected.

Our products risk exposure to product liability claims.

We are exposed to potential product liability risks, which are inherent in the testing, manufacturing and marketing of our products. We may incur significant expense investigating and defending any product liability claims, even if they do not result in liability. Moreover, even if no judgments, fines, damages or liabilities are imposed on us, our reputation could suffer, which could have a material adverse effect on our business, financial condition and results of operations.

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We are reliant upon two manufacturers for key ingredients of the manufacture of our hydrogels.

The Dow Chemical Company and the BASF Corporation are the principal manufacturers of the two polymers, polyethylene oxide and polyvinylpyrrolidone, respectively, that we primarily use in the manufacture of hydrogels. Although we have not experienced significant production delays attributable to supply changes, we believe that developing alternative sources of supply for the polymers used to make our current hydrogels would be difficult over a short period of time. Because we have no direct control over its third-party suppliers, interruptions or delays in the products and services provided by these third parties may be difficult to remedy in a timely fashion. In addition, if such suppliers are unable or unwilling to deliver the necessary raw materials or products, we may be unable to redesign or adapt our technology to work without such raw materials or products or find alternative suppliers or manufacturers. In such events, we could experience interruptions, delays, increased costs or quality control problems, which would have a material and adverse effect on our business, results of operations and financial condition.

There can be no assurance that our internal controls over financial reporting will be able to detect fraud or other issues.

We will be required under the Sarbanes-Oxley Act of 2002 to include a report of management on our internal controls that contains an assessment by management of the effectiveness of our internal control over financial reporting. Because and so long as we are an emerging growth company, our public accounting firm auditing our financial statements will not be required to report on the effectiveness of internal control over financial reporting, and our stockholders will not have the benefit thereof. Effective internal controls are necessary for us to provide reliable financial reports and effectively prevent fraud. However, a control system, no matter how well conceived and operated, can provide only reasonable, not absolute, assurance that the objectives of the control system are met. There can be no assurance that all control issues or fraud will be detected. In connection with the Merger, and as we continue to grow our business, our internal controls continue to become more complex and require more resources.

Our ability to provide customers with competitive services is dependent on our ability to attract and retain qualified personnel, including our senior management team.

Our ability to grow and provide our customers with competitive services is partially dependent on our ability to attract and retain highly motivated people with the skills necessary to serve our customers. Personnel with the requisite skills, qualifications, or security clearance may be in short supply or generally unavailable. The loss of personnel could impair our ability to perform under certain contracts, which could have a material adverse effect on our consolidated financial position, results of operations, prospects and cash flows.

In addition, due to the Merger, uncertainty around future employment opportunities, facility locations, organizational and reporting structures, and other related concerns may impair our ability to attract and retain qualified personnel. If employee attrition is higher than expected due to difficulties encountered in the integration process it may adversely impact our ability to realize the anticipated benefits of the Merger.

We may need to raise additional capital, and we cannot be sure that additional financing will be available.

Subsequent to the Spin-Off, we will need to fund our ongoing working capital, capital expenditure and operating requirements through cash flows from operations and new sources of capital, including additional financing. Our ability to obtain future financing will depend on, among other things, our financial condition, results of operations and prospects, as well as on the condition of the capital markets or other credit markets at the time we seek financing. Increased volatility and disruptions in the financial markets could make it more difficult and more expensive for us to obtain financing. In addition, the adoption of new statutes and regulations, the implementation of recently enacted laws or new interpretations or the enforcement of older laws and regulations applicable to the financial markets or the financial services industry could result in a reduction in the amount of available credit or an increase in the cost of credit. Historically, we have relied on Alliqua and its credit facilities and its access to capital for our financing needs but, after the Spin-Off, we will not have access to Alliqua’s financial resources. There can be no assurance that, as a new independent public company, we will have sufficient access to the capital markets on terms that we will we find acceptable.

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Changes in accounting standards and subjective assumptions, estimates and judgments by management related to complex accounting matters could significantly affect our financial results or financial condition.

GAAP and related accounting pronouncements, implementation guidelines and interpretations with regard to a wide range of matters that are relevant to our business, including but not limited to revenue recognition, business combinations, impairment of goodwill, indefinite-lived intangible assets and long-lived assets, inventory and equity-based compensation, are highly complex and involve many subjective assumptions, estimates and judgments. Changes in these rules or their interpretation or changes in underlying assumptions, estimates or judgments could significantly change our reported or expected financial performance or financial condition.

Our ability to pursue strategic acquisitions and partnerships may impact our ability to compete in the markets we serve.

Besides pursuing organic growth, we may explore potential strategic acquisitions that could allow us to expand our operations. However, we may be unable to identify attractive candidates or complete acquisitions on terms favorable to us. In addition, our ability to successfully integrate the operations we acquire and leverage these operations to generate revenue and earnings growth may significantly impact future revenue and earnings as well as investor returns. Integrating acquired operations is a significant challenge and there is no assurance that we will be able to manage such integrations successfully. Failure to successfully integrate acquired operations may adversely affect our cost structure, thereby reducing our margins and return on investment.

We have also entered into, and expect to seek to enter into, additional strategic partnerships with other industry participants as part of an effort to expand our business. However, we may be unable to identify attractive strategic partnership candidates or complete such partnerships on terms favorable to us. In addition, if we are unable to successfully implement our partnership strategies or our strategic partners do not fulfill their obligations or otherwise do not prove advantageous to our business, our investments in such partnerships and our anticipated business expansion could be adversely affected.

Achieving our growth objectives may prove unsuccessful. We may be unable to identify future attractive acquisitions and strategic partnerships, which may adversely affect our growth. In addition, our ability to consummate or integrate acquisitions or to consummate or implement our strategic partnerships may be materially and adversely affected.

Risks Relating to TOP’s Business

There is substantial uncertainty about TOP’s ability to continue as a going concern.

The report of TOP’s independent registered public accounting firm contains an explanatory paragraph as to its ability to continue as a going concern, which could prevent us from obtaining new financing on reasonable terms or at all.

Because TOP has recurring losses, negative cash flows from operating activities, and no cash on hand, the report of TOP’s independent registered public accounting firm, with respect to its financial statements at December 31, 2017, and for the year ended December 31, 2017, contains an explanatory paragraph as to TOP’s potential inability to continue as a going concern. This opinion indicates that substantial doubt exists regarding TOP’s ability to remain in business. Such an opinion may adversely affect our ability to obtain new financing on reasonable terms or at all.

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TOP may not be able to successfully develop its pharmaceutical business.

TOP’s ability to successfully develop its pharmaceutical business depends on its ability to collaborate with leading medical experts in drug development and clinical research, to identify, develop and commercialize new therapeutic approaches for the treatment of certain medical conditions and diseases as well as the symptoms of disease, to create unique therapeutics capable of patent or other intellectual property protection, and to compete with major pharmaceutical companies and other already established cannabis drug companies. TOP’s inability to successfully implement the above could have a detrimental impact on its pharmaceutical business.

TOP’s success will largely depend on the success of its drug candidates, the development of which will require significant capital resources and years of clinical development effort.

While TOP is in the process of conducting certain pre-clinical and clinical trials in Israel, TOP currently has no drug products on the market. TOP’s business depends almost entirely on the successful clinical development, regulatory approval and commercialization of its drug candidates. Investors need to be aware that substantial additional investments, including further clinical development and regulatory approval efforts, will be required before TOP is permitted to market and commercialize any drug candidates, and such commercialization may never occur. Clinical trials are subject to extensive and rigorous review and regulation by numerous government authorities in the United States, the European Union, Israel and other jurisdictions where TOP intends, if approved, to conduct research and development efforts and market its drug candidates. Before obtaining regulatory approvals for any of drug candidates, TOP must demonstrate through pre-clinical testing and clinical trials that the drug candidate is safe and effective for its specific application. This process generally is lengthy and may include post-marketing studies and surveillance, and is expected to require the expenditure of substantial resources. Of the large number of drugs in development for approval in the United States and the European Union, only a small percentage will successfully complete the FDA regulatory approval process or be granted authorization to be marketed in the European Commission or the other competent authorities in the European Union (“EU”) Member States. Accordingly, even if TOP obtains sufficient financing to fund its current and any additional planned research, development and clinical programs, TOP cannot provide any assurances that any of its drug candidates will be successfully developed or commercialized.

TOP may be unable to formulate or scale-up any or all of its drug candidates. There is no guarantee that any of these drug candidates will be able to be produced in a manner sufficient to meet the applicable criteria for product stability, content uniformity and all other criteria necessary for product approval in the United States and other markets. Any of TOP’s drug candidates may fail to achieve their specified endpoints in clinical trials. Furthermore, drug candidates may not be approved even if they achieve their specified endpoints in clinical trials. The FDA may disagree with TOP’s trial design and interpretation of data from clinical trials, or may change the requirements for approval even after it has reviewed and commented on the design for TOP’s clinical trials. The FDA may also approve a drug for fewer or more limited indications than TOP requests, or may grant approval contingent on the performance of costly post-approval clinical trials (i.e., Phase IV trials). In addition, the FDA may not approve the labeling claims that TOP believes are necessary or desirable for the successful commercialization of its drug candidates. TOP faces similar challenges in jurisdictions outside the U.S.

If TOP is unable to expand its pipeline and/or obtain regulatory approval for its drug candidates on the timelines it anticipates, TOP will not be able to execute its business strategy effectively and its ability to substantially grow its revenues will be limited, which could have a material adverse effect on the business, results of operations, financial condition and prospects of TOP.

TOP’s drug candidates may contain controlled substances the use of which may generate public controversy.

Since TOP’s drug candidates may contain controlled substances, their regulatory approval may generate public controversy. Political and social pressures and adverse publicity could lead to delays in approval of, and increased expenses for, TOP’s drug candidates. These pressures could also limit or restrict the introduction and marketing of its drug candidates. Adverse publicity from cannabis misuse or adverse side effects from cannabis or other cannabinoid-derived drugs may adversely affect the commercial success

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or market penetration achievable by its drug candidates. The nature of its business will likely attract a high-level of public and media interest, and in the event of any resultant adverse publicity, TOP’s reputation may be harmed.

TOP’s drug candidates are derived from cannabinoid strains which are marketed and sold by unaffiliated third parties in certain states within the U.S., Canada, Australia and elsewhere under licenses from TOL or sublicenses from TOG. TOP cannot control the products sold or claims asserted by such third parties, and no assurance can be given that any such claims might not adversely affect TOP’s ability to obtain regulatory approval of its drug candidate products.

TOP’s products or prospective products may become subject to U.S. controlled substance laws and regulations.

TOP’s products and prospective products are likely to contain controlled substances as defined in the U.S. federal Controlled Substances Act of 1970, or CSA. Controlled substances that are pharmaceutical products are subject to a high degree of regulation under the CSA, which establishes, among other things, certain registration, manufacturing quotas, security, recordkeeping, reporting, import, export and other requirements administered by the DEA. The DEA classifies controlled substances into five schedules: Schedule I, II, III, IV or V substances. Schedule I substances by definition have a high potential for abuse, no currently “accepted medical use” in the U.S., lack accepted safety for use under medical supervision, and may not be prescribed, marketed or sold in the U.S. Pharmaceutical products approved for use in the U.S. which contain a controlled substance are listed as Schedule II, III, IV or V, with Schedule II substances considered to present the highest potential for abuse or dependence and Schedule V substances the lowest relative risk of abuse among such substances. Schedule I and II drugs are subject to the strictest controls under the CSA, including manufacturing and procurement quotas, security requirements and criteria for importation. In addition, dispensing of Schedule II drugs is also restricted. For example, they may not be refilled without a new prescription.

While cannabis is a Schedule I controlled substance, products approved for medical use in the U.S. that contain cannabis or cannabis extracts should be placed in Schedules II-V, since approval by the FDA satisfies the “accepted medical use” requirement. If and when any of TOP’s prospective products receive FDA approval, the DEA will make a scheduling determination and place it in a schedule other than Schedule I for it to be prescribed for patients in the United States. If approved by the FDA, TOP expects the finished dosage forms of any of its drug candidates to be listed by the DEA as a Schedule II or III controlled substance. Consequently, their manufacture, importation, exportation, domestic distribution, storage, sale and legitimate use will be subject to a significant degree of regulation by the DEA. The scheduling process may take one or more years beyond FDA approval, thereby significantly delaying the launch of TOP’s drugs. However, the DEA must issue a temporary order scheduling the drug within 90 days after the FDA approves the drug and the DEA receives a scientific and medical evaluation and scheduling recommendation from the Department of Health and Human Services. Furthermore, if the FDA, DEA or any foreign regulatory authority determines that any of TOP’s drugs may have potential for abuse, it may require us to generate more clinical data than that which is currently anticipated, which could increase the cost and/or delay the launch of TOP’s drugs.

Controlled substance legislation differs between countries and legislation in certain countries may restrict or limit TOP’s ability to sell its proposed cannabis-based products and/or their use in medical treatments.

Most countries are parties to the Single Convention on Narcotic Drugs 1961 and its successor treaties, which governs international trade and domestic control of narcotic substances, including cannabis extracts. Countries may interpret and implement their treaty obligations in ways that create a legal obstacle to obtaining approval for TOP’s products and the prospective use of these products in various medical treatments. These countries and any country with similar obstacles may not be willing or able to amend or otherwise modify their laws and regulations to allow TOP’s products or prospective products to be marketed and treatments to be administered, which would adversely affect TOP’s business, operations, financial condition and prospects.

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Changes in consumer preferences and acceptance of cannabinoid-based medical products and treatments and any negative trends could adversely affect TOP’s business.

TOP is substantially dependent on initial and continued market acceptance and proliferation of cannabinoid-based drugs and treatments. TOP believes that as cannabinoid-derived drugs become more widely accepted by the medical and scientific communities and the public at large, the stigma associated with cannabinoid-derived drugs and treatments will moderate and, as a result, consumer demand will likely continue to grow; however, TOP cannot predict the future growth rate and size of the market, or that the regulatory framework will be favorable, of which there can be no assurance. Any negative trend in outlook on cannabinoid-based medical products would adversely affect TOP’s business prospects. Further, TOP cannot provide any assurance that any of its drug candidates will achieve the expected market acceptance and revenue, if and when it obtains the necessary regulatory approvals.

In addition, the market acceptance of any drug depends on a number of factors, including the indication statement and warnings approved by regulatory authorities for the drug label, continued demonstration of efficacy and safety in commercial use, physicians’ willingness to prescribe the drug, reimbursement from third-party payers such as government health care systems and insurance companies, the price of the drug, the nature of any post-approval risk management plans mandated by regulatory authorities, competition, and marketing and distribution support. Any factors preventing or limiting the market acceptance of TOP’s drugs could have a material adverse effect on the business, results of operations, financial condition and prospects of TOP.

The pharmaceutical industry is well-funded with a strong and experienced lobbying presence at both the federal and state levels, as well as internationally, that surpasses financial resources of the current group of medical cannabinoid research and development companies.

Some believe that large, well-funded pharmaceutical and other related businesses and industries may have material economic reasons to be in strong opposition to cannabinoid-based drugs, and anecdotal reports indicate that the pharmaceutical industry has provided funding to oppose cannabis legal reform efforts. Continued or increased effort by the pharmaceutical lobby opposing cannabinoid products could or might impede or delay the development of cannabinoid-based drugs and could have a detrimental impact on the business, results of operations, financial condition and prospects of TOP.

Clinical trials of cannabinoid-based drug candidates and treatments are risky, in part because they are novel, with very limited or non-existing clinical trial history.

While TOP is encouraged by the limited preliminary results of its pre-clinical studies and clinical trials and the clinical trials of others, TOP cannot provide any assurance regarding any conclusions from or proof that its assumptions for any trials are scientifically compelling, or that any clinical trial will result in commercially viable drugs or treatments. Furthermore, no officer or manager of TOP other than Seth Yakatan, TOP’s CEO, and Dr. Mitchell Glass, TOP’s Chief Medical Officer, has a direct record of accomplishing or conducting such scientific studies, and TOP does not have an internal infrastructure capable of conducting clinical trials. As a result, TOP faces a significant risk that requires it to use outsourced researchers for studies or trials, which is and may continue to be highly costly.

Clinical trials are expensive, time consuming and difficult to design and implement. TOP, as well as the applicable regulatory authorities, may suspend, delay or terminate TOP’s clinical trials at any time, may require TOP, for various reasons, to conduct additional clinical trials, or may require a particular clinical trial to continue for a longer duration than originally planned, including, among others:

•

lack of effectiveness of any formulation or delivery system during clinical trials;

•

discovery of serious or unexpected toxicities or drug-related side effects experienced by trial participants or other safety issues;

•

slower than expected rates of subject recruitment and enrollment rates in clinical trials;

•

delays in reaching or failing to reach agreement on acceptable terms with prospective clinical trial sites, the terms of which can be subject to extensive negotiation and may vary significantly among different clinical trial sites;

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•

delays, capacity constraints or other inability to manufacture or otherwise obtain sufficient quantities of materials for use in clinical trials due to regulatory, manufacturing or other limitations;

•

delays in obtaining regulatory authorization to commence a trial, including DEA, FDA or Institutional Review Board (“IRB”) approvals, licenses or waivers required for obtaining and using cannabis or cannabinoid derived substances for research, either before or after a trial is commenced;

•

unfavorable results from ongoing pre-clinical studies and clinical trials;

•

patients or investigators failing to comply with study protocols;

•

patients failing to return for post-treatment follow-up at the expected rate;

•

sites participating in an ongoing clinical study withdrawing, requiring us to engage new sites;

•

third-party clinical investigators declining to participate in TOP’s clinical studies, not performing the clinical studies on the anticipated schedule, or acting in ways inconsistent with the established investigator agreement, clinical study protocol, good clinical practices, or other IRB requirements;

•

third-party entities not performing data collection and analysis in a timely or accurate manner or at all; or

•

regulatory inspections of TOP’s clinical studies that require it to undertake corrective action or suspend or terminate its clinical studies, including DEA or comparable foreign regulatory authority-related recordkeeping, reporting or security violations at a clinical trial site.

Any of the foregoing could have a material adverse effect on the business, results of operations, financial condition and prospects of TOP.

Results of preclinical studies and earlier clinical trials are not necessarily predictive indicators of future results.

Any positive results from pre-clinical testing of TOP’s drug candidates and clinical trials may not necessarily be predictive of the results from Phase 1, Phase 2 or Phase 3 clinical trials. In addition, TOP’s interpretation of results derived from clinical data or its conclusions based on its pre-clinical data may prove inaccurate. Frequently, pharmaceutical and biotechnology companies have suffered significant setbacks in clinical trials after achieving positive results in pre-clinical testing and early clinical trials, and TOP cannot be certain that it will not face similar setbacks. These setbacks may be caused by pre-clinical and clinical data being susceptible to varying interpretations and analyses. Furthermore, certain drug candidates may perform satisfactorily in pre-clinical studies and clinical trials, but nonetheless fail to obtain FDA approval, a marketing authorization granted by the European Commission, or appropriate approvals by government authorities in other countries. If TOP fails to produce positive results in its clinical trials for its drug candidates, the development timeline and regulatory approval and commercialization prospects for them, as well as the results of TOP’s business, results of operations, financial condition and prospects, would be materially adversely affected.

The regulatory approval processes with the FDA, the European Medicines Agency (the “EMA”) and other comparable foreign regulatory authorities are lengthy and inherently unpredictable.

TOP is not permitted to market its drug candidates in the United States or the European Union until it receives approval of a New Drug Application (“NDA”) from the FDA or a Marketing Authorization Application (“MAA”) from the European Commission, respectively, or in any foreign countries until it receives the approval from the regulatory authorities of such countries. Prior to submitting an NDA to the FDA or an MAA to the EMA for approval of its drug candidates, TOP will need to have completed its pre-clinical studies and clinical trials. Successfully completing any clinical program and obtaining approval of an NDA or MAA is a complex, lengthy, expensive and uncertain process, and the FDA or EMA may delay, limit or deny approval of drug candidates for many reasons, including, among others:

•

an inability to demonstrate that TOP’s drug candidates are safe and effective in treating patients to the satisfaction of the FDA or EMA;

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•

results of clinical trials that may not meet the level of statistical or clinical significance required by the FDA or EMA;

•

disagreements with the FDA or EMA with respect to the number, design, size, conduct or implementation of clinical trials;

•

requirements by the FDA and EMA to conduct additional clinical trials;

•

disapproval by the FDA or EMA or other applicable foreign regulatory authorities of certain formulations, labeling or specifications of drug candidates;

•

findings by the FDA or EMA that the data from preclinical studies and clinical trials is insufficient;

•

the FDA or EMA may disagree with the interpretation of data from preclinical studies and clinical trials; and

•

the FDA, European Commission or other applicable foreign regulatory agencies may change their approval policies or adopt new regulations.

Any of these factors, many of which are beyond TOP’s control, could increase development costs or jeopardize TOP’s ability to obtain regulatory approval for its drug candidates.

TOP may apply for orphan drug status granted by the FDA for some of its drug candidates for the treatment of rare diseases, and orphan drug status does not prevent the FDA from approving a different drug for the same disease or condition, or the same drug for a different disease or condition.

Regulatory authorities in some jurisdictions, including the United States and the European Union, may designate drugs for relatively small patient populations as orphan drugs. The FDA may grant orphan drug designation to drugs intended to treat a rare disease or condition that affects fewer than 200,000 individuals annually in the United States. In the European Union, the EMA’s Committee for Orphan Medicinal Products grants orphan drug designation to promote the development of drugs that are intended for the diagnosis, prevention or treatment of life-threatening or chronically debilitating conditions affecting not more than five in 10,000 persons in the European Union. Additionally, such designation is granted for drugs intended for the diagnosis, prevention or treatment of a life-threatening, seriously debilitating or serious and chronic condition and when, without incentives, it is unlikely that sales of the drug in the European Union would be sufficient to justify the necessary investment in developing the drug.

In the United States, orphan drug designation entitles a party to financial incentives, such as opportunities for grant funding towards clinical trial costs, tax credits for certain research and user fee waivers under certain circumstances. In addition, if a drug receives the first FDA approval for the drug and indication for which it has orphan drug designation, the drug is entitled to seven years of market exclusivity, which means the FDA may not approve any other application for the same drug for the same indication for a period of seven years, except in limited circumstances, such as a showing of clinical superiority over the drug with orphan drug exclusivity.

Orphan drug exclusivity does not prevent the FDA from approving a different drug for the same disease or condition, or the same drug for a different disease or condition. In the European Union, orphan drug designation also entitles a party to financial incentives such as reduction of fees or fee waivers and ten years of market exclusivity following drug approval. This period may be reduced to six years if the orphan drug designation criteria are no longer met, including where it is shown that the drug is sufficiently profitable so that market exclusivity is no longer justified.

TOP expects to face intense competition, often from companies with greater resources and experience than TOP has.

Demand for cannabinoid-derived drugs will likely be dependent on a number of social, political and economic factors that are beyond TOP’s control. While TOP believes that there will be a demand for such drugs, and that the demand will grow, there is no assurance that such demand will happen, that TOP will benefit from any demand or that its business, in fact, will ever generate revenues from its drug development activities or become profitable.

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The emerging market for cannabinoid-derived drugs and medical research and development is and will likely remain competitive. The development and commercialization of drugs is highly competitive. TOP competes with a variety of multinational pharmaceutical companies and specialized biotechnology companies, as well as products and processes being developed by universities and other research institutions. Many of TOP’s competitors have developed, are developing, or will develop drugs and processes competitive with its drug candidates. Competitive therapeutic treatments include those that have already been approved and accepted by the medical community and any new treatments that may enter the market. For some of TOP’s drug development candidates, other treatment options are currently available, under development, and may become commercially available in the future. If any of TOP’s drug candidates is approved for the diseases and conditions it is currently pursuing, they may compete with a range of therapeutic treatments that are either in development or currently marketed.

TOP is aware of many companies that are engaged in cannabinoid-derived drug development activities. In addition, other U.S.-based and foreign-based companies are in early stage discovery and preclinical development utilizing the cannabinoids CBD and/or THC, as well as other cannabinoids.

Established companies may have a competitive advantage over TOP due to their size and experience, financial resources, and institutional networks. Many of TOP’s competitors may have significantly greater financial, technical and human resources than TOP. Due to these factors, TOP’s competitors may have an advantage in marketing their approved drugs and may obtain regulatory approval of their drug candidates before TOP is able to, which may limit its ability to develop or commercialize its drug candidates. TOP’s competitors may also develop drugs that are safer, more effective, more widely used and less expensive. These advantages could materially impact TOP’s ability to develop and, if approved, commercialize its drug candidates successfully. Furthermore, some of these competitors may make acquisitions or establish collaborative relationships among themselves or with third parties to increase their ability to rapidly gain market share.

TOP’s drug candidates may compete with other plant-derived or synthetic cannabinoid drugs, in addition to competing with state-licensed medical and adult-use cannabis, in markets where the medical and/or adult use of cannabis is legal. There is continuing support in the United States for further state legalization of cannabis. In markets where medical and/or adult-use cannabis is not legal, TOP’s drug candidates, once approved by regulators, may compete with cannabis or cannabis-based products purchased in the illegal drug market.

As generic versions of drug products enter the market, the price for such drugs may be expected to decline rapidly and substantially. Even if TOP is the first to obtain FDA approval of one of its drug candidates, the future potential approval of generics could adversely affect the price it is able to charge and the profitability of its product would likely decline.

Mergers and acquisitions in the pharmaceutical and biotechnology industries may result in more resources being concentrated among a smaller number of TOP’s competitors. Smaller and other early-stage companies may also prove to be significant competitors, particularly through collaborative arrangements with large and established companies. These companies may compete with TOP in recruiting and retaining qualified scientific, management and commercial personnel, establishing clinical trial sites and subject registration for clinical trials, as well as in acquiring technologies complementary to TOP’s research projects.

Product shipment delays could have a material adverse effect on TOP’s business, results of operations, financial condition and prospects.

The shipment, import and export of any products which TOP develops require import and export licenses. In the U.S., the FDA, U.S. Customs and Border Protection and the DEA, and in the United Kingdom, the Home Office, and in other countries, similar regulatory authorities regulate the import and export of pharmaceutical products that contain controlled substances. TOP may not be granted, or if granted, maintain, such licenses from the authorities in certain countries. Even if TOP obtains the relevant licenses, shipments of any products which TOP develops may be held up in transit, which could cause significant delays and may lead to product batches being stored outside required temperature ranges. Inappropriate storage may damage product shipments, resulting in a partial or total

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loss of revenue from one or more shipment of any products which TOP develops. A partial or total loss of revenue from one or more shipments could have a material adverse effect on TOP’s business, results of operations, financial condition and prospects.

Failure to obtain regulatory approval in jurisdictions outside the United States, Israel and the European Union would prevent TOP’s drug candidates from being marketed in those jurisdictions.

To market and sell TOP’s future drugs in jurisdictions other than the United States, Israel and the European Union, TOP must obtain separate marketing approvals and comply with numerous and varying regulatory requirements. The regulatory approval process outside the United States, Israel and the European Union generally includes all of the risks associated with obtaining FDA approval or approval from the Israeli Ministry of Health or the European Commission but may involve additional testing.

TOP may need to partner with third parties to obtain approvals outside the United States, Israel and the European Union. In addition, in many countries worldwide, it is required that the drug be approved for reimbursement before the drug can be approved for sale in that country. TOP may not obtain approvals from regulatory authorities outside the United States, Israel and the European Union on a timely basis, if at all. Even if TOP were to receive approval in the United States, Israel or the European Union, such approval does not ensure approval by regulatory authorities in other countries or jurisdictions. Similarly, approval by one regulatory authority outside the United States, Israel and the European Union would not ensure approval by regulatory authorities in other countries or jurisdictions or by the FDA, Israeli Ministry of Health or the European Commission. If TOP is unable to obtain approval of its drug candidates by regulatory authorities in other foreign jurisdictions, the commercial prospects of those drug candidates may be significantly reduced, and this could have a material adverse effect on TOP’s business, results of operations, financial condition or prospects.

Laws and regulations affecting therapeutic uses of cannabinoids are constantly evolving and the legalization and use of medical and recreational cannabis in the U.S. and elsewhere may impact TOP’s business.

There is a substantial amount of change occurring in the U.S. regarding the use of medical and adult-use cannabis products. While cannabis products not approved by FDA are Schedule I substances as defined under federal law, and their possession and use is not permitted according to federal law, 34 states in the United States, plus the District of Columbia, Puerto Rico and Guam, have legalized the use of medical cannabis. Ten states, plus the District of Columbia, that have legalized the use of adult-use cannabis. Sixteen states have legalized high-CBD, low-THC oils for a limited class of patients and 13 states, plus the U.S. Virgin Islands, have decriminalized cannabis, which generally means that there is no arrest, prison time, or criminal record for the first-time possession of a small amount of cannabis for personal consumption. The 2018 U.S. Farm Bill, de-scheduled CBD extracts and other material derived from certain hemp plants with extremely low THC content, although the marketing of such products for medical or other purposes would still be subject to regulatory premarketing approval requirements and other applicable laws and regulations, including by the FDA. Although TOP’s business is quite distinct from that of medical cannabis companies, future legislation authorizing the sale, distribution, use, and insurance reimbursement of non-FDA approved cannabis products could affect its business, results of operations, financial condition or prospects.

The potential ongoing evolution of laws and regulations affecting the research and development of cannabinoid-based medical drugs and treatments could detrimentally affect TOP’s business. Laws and regulations related to the therapeutic uses of cannabinoid-based drugs may be subject to changing interpretations. These changes may require TOP to incur substantial costs associated with legal and compliance fees and may ultimately require TOP to alter its business plan. Furthermore, violations or alleged violation of these laws could disrupt TOP’s business and result in a material adverse effect on its business, results of operations and financial condition. In addition, TOP cannot predict the nature of any future laws, regulations, interpretations or applications of laws and regulations and it is possible that new laws and regulations may be enacted in the future that will be directly applicable to its business.

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TOP’s failure to comply with existing and potential future laws and regulations relating to drug development could harm its business.

TOP’s business is, and will be, subject to wide-ranging existing federal and state laws and regulations and other governmental bodies in each of the countries it may develop and/or market its drug candidates. TOP must comply with all regulatory requirements if it expects to be successful.

If any of TOP’s cannabinoid-derived drug candidates are approved in the United States, they will be subject to ongoing regulatory requirements, including federal and state requirements. As a result, TOP and its collaborators and/or joint venture partners must continue to expend time, money and effort in all areas of regulatory compliance, including, if applicable, manufacturing, production, quality control and assurance and clinical trials. TOP will also be required to report certain adverse reactions and production problems, if any and applicable, to the FDA, and to comply with advertising and promotion requirements for its cannabinoid-derived drug candidates.

Any failure to comply with ongoing regulatory requirements may significantly and adversely affect its ability to conduct clinical trials which are prerequisites to its ability to commercialize TOP’s cannabinoid-based drugs and related treatments. If regulatory sanctions are applied or if regulatory approval, once obtained, is for any reason withdrawn, TOP’s business, results of operations, financial condition or prospects could be materially adversely affected.

Healthcare legislation, including potentially unfavorable pricing regulations or other healthcare reform initiatives, may increase the difficulty and cost for TOP to obtain marketing approval of and commercialize its product candidates.

In the United States, there have been a number of legislative and regulatory changes and proposed changes regarding the healthcare system that could prevent or delay marketing approval of TOP’s product candidates, restrict or regulate post-approval activities or affect its ability to profitably sell any product candidates for which it obtains marketing approval.

The Patient Protection and Affordable Care Act, as amended by the Health Care and Education Reconciliation Act, or Affordable Care Act, among other things, imposes a significant annual fee on companies that manufacture or import branded prescription drug products. It also contains substantial provisions intended to broaden access to health insurance, reduce or constrain the growth of healthcare spending, enhance remedies against healthcare fraud and abuse, add new transparency requirements for the healthcare and health insurance industries, impose new taxes and fees on pharmaceutical and medical device manufacturers, and impose additional health policy reforms, any of which could negatively impact TOP’s business, results of operations, financial condition or prospects. The Affordable Care Act is likely to continue the downward pressure on pharmaceutical and medical device pricing, especially under the Medicare program, and may also increase TOP’s regulatory burdens and operating costs.

TOP expects that the Affordable Care Act, as well as other healthcare reform measures that have been and may be adopted in the future, may result in more rigorous coverage criteria and in additional downward pressure on the price that it receives for any approved product, and could seriously harm its future revenues. Any reduction in reimbursement from Medicare or other government programs may result in a similar reduction in payments from private payors. The implementation of cost containment measures or other healthcare reforms may compromise its ability to generate revenue, attain profitability or commercialize TOP’s products. In addition, other legislative changes have been proposed and adopted since passage of the Affordable Care Act. If TOP ever obtains regulatory approval and commercializes its products, new laws may result in additional reductions in Medicare and other healthcare funding, which could have a material adverse effect on TOP’s customers and accordingly, its business, results of operations, financial condition or prospects.

Even if TOP is able to commercialize its products, the products may not receive coverage and adequate reimbursement from third-party payors, which could harm its business.

The availability of reimbursement by governmental and private payors is essential for most patients to be able to afford expensive drug treatments. Sales of TOP’s products, if approved, will depend substantially on the extent to which the costs of these products will be paid by health maintenance, managed care,

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pharmacy benefit and similar healthcare management organizations, or reimbursed by government health administration authorities, private health coverage insurers and other third-party payors. If reimbursement is not available, or is available only to limited levels, TOP may not be able to successfully commercialize its products. Even if coverage is provided, the approved reimbursement amount may not be high enough to allow TOP to establish or maintain pricing sufficient to realize a sufficient return on TOP’s investment.

There is significant uncertainty related to the insurance coverage and reimbursement of newly approved products, including cannabinoid-based products. In the United States, the principal decisions about reimbursement for new medicines are typically made by the Centers for Medicare & Medicaid Services, or “CMS”, an agency within the U.S. Department of Health and Human Services, or “HHS”, as CMS decides whether and to what extent a new medicine will be covered and reimbursed under Medicare. Furthermore, private payors often follow Medicare coverage policies and payment limitations in setting their own reimbursement rates. Therefore, any reduction in reimbursement that results from the Medicare Modernization Act may result in a similar reduction in payments from private payors. In the United States, the Medicare Prescription Drug, Improvement, and Modernization Act of 2003, or “Medicare Modernization Act”, established the Medicare Part D program and provided authority for limiting the number of drugs that will be covered in any therapeutic class thereunder. The Medicare Modernization Act, including its cost reduction initiatives, could decrease the coverage and reimbursement rate that TOP receives for any of its approved products.

The intended use of a drug product by a physician can also affect pricing. For example, CMS could initiate a National Coverage Determination administrative procedure, by which the agency determines which uses of a therapeutic product would and would not be reimbursable under Medicare. This determination process can be lengthy, thereby creating a long period during which the future reimbursement for a particular product may be uncertain.

Outside the United States, including in member states of the European Union, the pricing of prescription drugs often is subject to governmental control. In these countries, pricing negotiations or the successful completion of health technology assessment procedures with governmental authorities can take considerable time after receipt of marketing approval for a product. In addition, there can be considerable pressure by governments and other stakeholders on prices and reimbursement levels, including as part of cost containment measures. Certain countries allow companies to fix their own prices for medicines but monitor and control company profits. Political, economic and regulatory developments may further complicate pricing negotiations, and pricing negotiations may continue after reimbursement has been obtained. Reference pricing used by various European Union member states and parallel distribution, or arbitrage between low-priced and high-priced member states, can further reduce prices. In some countries, TOP or its collaborators may be required to conduct a clinical trial or other studies that compare the cost-effectiveness of its product candidates to other available therapies in order to obtain or maintain reimbursement or pricing approval. Publication of discounts by third-party payors or authorities may lead to further pressure on the prices or reimbursement levels within the country of publication and other countries. If reimbursement of any product candidate approved for marketing is unavailable or limited in scope or amount, or if pricing is set at unsatisfactory levels, TOP’s business, financial condition, results of operations or prospects could be adversely affected.

TOP is an early stage company with limited operating history or experience.

TOP is an early stage company with no operating revenue to date. As such, it is extremely difficult to make accurate predictions and forecasts of its finances and prospective investors do not have a significant operating history upon which to evaluate TOP’s ability to achieve its current business plan and future objectives. This is compounded by operating in the pharmaceutical industry, which is rapidly transforming. There can no assurance that TOP’s products or services will be or remain attractive to potential and current. Furthermore, TOP’s management may have limited insight into trends that might emerge and could materially affect TOP’s business, results of operations, financial condition or prospects.

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TOP has experienced substantial cash flow and financing constraints.

TOP’s business has generated net losses and negative cash flows from operating activities since its inception. In the near term, TOP expects that its net losses and cash used in operating activities will increase as compared to prior periods as it increases its development activities. TOP expects to incur additional losses as it continues to research and develop drug candidates and conduct clinical trials, and in any event, until its revenues exceed its expenses. Even if TOP succeeds in obtaining regulatory approval to market its products, it may still incur losses for the foreseeable future.

Managers of TOP may pursue other ventures.

The obligations to TOP of its managers and executive officers are not exclusive, and TOP’s managers and executive officers may be involved in other business activities. Liabilities incurred and commitments undertaken by officers, members, managers or general partners with respect to projects other than TOP’s business could adversely affect their ability to manage TOP. Such activities could compete with TOP and/or result in a conflict of interest. Conflicts of interest may expose TOP to the risks, among others, that such persons’ allocation of time to TOP, or that decisions made on behalf of TOP, or transactions entered into between TOP and such persons may not reflect the best interests of TOP or its members from their perspective.

The directors and officers and a small number of stockholders will own a large percentage of AquaMed’s equity and such directors and officers will have the ability to control matters affecting AquaMed’s stockholders.

The directors and officers of AquaMed beneficially own approximately 12.9% of AquaMed’s outstanding shares of common stock, and together with four additional stockholders would beneficially own a majority of AquaMed’s outstanding shares of common stock. The AquaMed shareholders elect TOP’s Board of Directors and have the ability to control the acquisition or disposition of TOP’s assets, and the future issuance of its capital stock. Accordingly, other shareholders will find it impossible to replace TOP’s directors if they disagree with the way TOP’s business is being operated. Because the influence by these insiders could result in management making decisions that are in the best interest of those insiders and not in the best interest of the shareholders, shareholders may lose some or all of the value of their investment in AquaMed.

If TOP is unable to meet its future capital needs, TOP may be required to reduce or curtail operations or shut down completely.

TOP’s future capital requirements will depend on many factors, including:

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its ability to successfully implement its business objectives and strategic growth plans;

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its ability to obtain and maintain relationships with third-parties conducting pre-clinical studies and clinical trials and such persons fulfilling their obligations;

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development of novel pharmaceutical products;

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market acceptance of its drug candidates, once approved for sale;

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generating cash flow from operations;

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locating and retaining talent; and

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market and regulatory developments.

Based on TOP’s current financial situation, it may have difficulty continuing its operations at its current level, or at all, if it does not raise additional financing in the near future. Although TOP currently has no specific arrangements for additional financing, TOP intends to raise funds through private placements, public offerings or other financings. Sources of debt financing may result in high interest expense or be difficult to procure and would increase the liabilities and future cash commitments of TOP. Any financing, if available, may be on unfavorable terms, and TOP may be forced to relinquish rights to its proprietary compounds, technology or other intellectual property or marketing rights, which could result in the receipt of only a portion of any revenue that may be generated from a partnered product or business. If

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adequate funds are not obtained, TOP may be required to reduce, curtail, or discontinue operations. There is no assurance that TOP’s cash flow will be adequate to satisfy its existing operating expenses and capital requirements. In addition, if TOP issues equity or convertible debt securities to raise additional funds, its existing shareholders may experience substantial dilution, and the new equity or debt securities may have rights, preferences and privileges senior to those of existing shareholders.

There is no assurance that TOP will generate significant revenues, earn profits or pay distributions.

There is no assurance as to whether TOP will generate significant revenues, be profitable, or pay dividends or distributions to its members. TOP anticipates that it will continue to incur substantial expenses relating to the development and operation of its business for the foreseeable future. TOP currently intends to retain any future earnings for reinvestment in TOP’s business until TOP generates sufficient excess cash flow to pay dividends or distributions.

The payment and amount of any future distributions will be made at the discretion of the Board of Directors of AquaMed, and will depend upon, among other things, the results of TOP’s operations, cash flows and financial condition, operating and capital requirements, and other factors as the Board considers relevant. There is no assurance that future dividends or distributions will be paid, and, if dividends or distributions are paid, there is no assurance with respect to the amount of any such dividends or distributions.

TOP may not be able to effectively manage its growth and operations, which could materially and adversely affect its business, results of operations, financial condition and prospects.

TOP may in the future experience rapid growth and development in a relatively short period of time. The management of this growth will require, among other things, continued development of TOP’s financial and management controls and management information systems, stringent control of costs, the ability to attract and retain qualified management personnel and the training of new personnel. TOP intends to utilize outsourced resources, and hire additional personnel, in order to manage its expected growth and expansion. Failure to successfully manage its possible growth and development could have a material adverse effect on the business, results of operations, financial condition and prospects of TOP.

TOP may be unable to adequately protect its proprietary and intellectual property rights.

TOP’s ability to compete may depend on the superiority, uniqueness and value of its intellectual property and technology, including both internally developed intellectual property and technology and intellectual property licensed from third parties such as TOL. To the extent TOP is able to do so, in order to protect the proprietary rights of TOP and/or TOL, TOP intends to rely on a combination of patent, trademark, copyright and trade secret laws, confidentiality agreements with its employees and third parties, and protective contractual provisions. Despite these efforts, any of the following occurrences may reduce the value of TOP’s intellectual property:

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U.S. federal trademark and patent protection may not be available for the intellectual property of TOP due to the current classification of cannabis and CBD as a Schedule I controlled substance;

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The market for TOP’s products and services may depend to a significant extent upon the goodwill associated with its patents, trademarks and trade names, and its ability to register its intellectual property under U.S. federal and state law may be impaired by the illegality of cannabis and related drug paraphernalia under U.S. federal law;

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Patents containing cannabinoid-derived compositions and/or methods industry involve complex legal and scientific questions and patent protection may not be available for some products, strains or brands;

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Certain products based on previously known cannabinoids found in nature may not be subject to effective patent protection;

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TOP’s pending patent applications, provisional patent applications and applications for trademarks and copyrights relating to its business may not be granted and, if granted, may be challenged or invalidated;

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Issued patents, trademarks and registered copyrights may not provide TOP with any competitive advantages;

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TOP’s efforts to protect its intellectual property rights may not be effective in preventing misappropriation of any of its technology, products or intellectual property;

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TOP’s efforts may not prevent the research, development and design by others of products or technologies similar to or competitive with, or superior to those TOP develops;

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Another party may obtain a blocking patent and TOP would need to either obtain a license or design around the patent in order to continue to offer the contested feature or service in its products; or

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Much of the intellectual property which TOP utilizes, including certain cannabis strains, is owned by TOL, and is licensed by TOP pursuant to the licenses therefrom. In the event that such license was terminated, TOP would no longer be permitted to use such intellectual property. In such event, the resources where TOP had invested therein would have been wasted.

In addition, TOP does not know whether any of the pending patent applications or provisional patents for any of its drug candidates will result in the issuance of patents. The patent positions of biotechnology and pharmaceutical companies generally are highly uncertain, involve complex legal and factual questions and have often been the subject of litigation. As a result, the issuance, scope, validity, enforceability and commercial value of any of TOP’s potential future patents are highly uncertain. The steps TOP will take to protect its proprietary rights may not be adequate to preclude misappropriation of its proprietary information or infringement of its intellectual property rights, both inside and outside the United States. Patent examination processes may require TOP to narrow the claims for its pending patent applications, which may limit the scope of patent protection that may be obtained if the patents are granted. The rights to be granted under future patents issued to TOP may not provide TOP with the proprietary protection or competitive advantages it seeks. If TOP is unable to obtain and maintain patent protection for its technology and drugs, or if the scope of the patent protection obtained is not sufficient, TOP’s competitors could develop and commercialize technology and drugs similar or superior to TOP’s, and its ability to successfully commercialize its technology and drugs may be adversely affected.

The issuance of a patent may not always be conclusive as to its inventorship, scope, validity or enforceability. TOP’s issued patents may be challenged in the courts or patent offices in the U.S. and abroad. Such challenges may result in the loss of patent protection, the narrowing of claims in such patents or the invalidity or unenforceability of such patents, which could limit TOP’s ability to stop others from using or commercializing similar or identical technology and drugs, or limit the duration of the patent protection for TOP’s technology and drugs.

Federal trademark and patent protection may not be available for the intellectual property of TOP due to the current classification of cannabis and CBD as a Schedule I controlled substance.

As long as cannabis remains illegal under U.S. federal law as a Schedule I controlled substance pursuant to the CSA, the benefit of certain federal laws and protections which may be available to most businesses, such as federal trademark and patent protection regarding the intellectual property of a business, may not be available to TOP in the United States. As a result, TOP’s intellectual property may never be adequately or sufficiently protected against the use or misappropriation by third-parties in the United States. In addition, since the regulatory framework of the cannabis industry is in a constant state of flux, TOP can provide no assurance that it will ever obtain any protection of its intellectual property, whether on a federal, state or local level in the United States.

Costly litigation may be necessary to protect TOP’s intellectual property rights and TOP may be subject to claims alleging the violation of the intellectual property rights of others.

TOP may face significant expense and liability due to litigation or other proceedings relating to patents and other intellectual property rights of others. If another party has also filed a patent application or been issued a patent relating to an invention or technology claimed by TOP in pending applications, TOP may be required to participate in an interference proceeding declared by the U.S. Patent and Trademark Office to

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determine priority of invention, which could result in substantial uncertainties and costs for TOP, even if the eventual outcome were favorable to TOP. TOP or TOL also could be required to participate in interference proceedings involving issued patents and pending applications of another entity. An adverse outcome in an interference proceeding could require TOP to cease using the technology or to license rights from prevailing third parties.

The cost to TOP of any patent application or patent litigation, even if resolved in TOP’s favor, could be substantial. TOP’s ability to enforce its patent protection could be limited by its financial resources, and may be subject to lengthy delays.

A third party may claim that TOP uses inventions claimed by their patents and may go to court to stop TOP from engaging in research, development and/or the sale of any of TOP’s future drugs. Such lawsuits are expensive and would consume time and other resources. There is a risk that the court will decide that TOP is infringing on the third party’s patents and will order TOP to stop the activities claimed by the patents. In addition, there is a risk that a court will order TOP to pay the other party damages for having infringed their patents.

Moreover, there is no assurance that any prevailing patent owner would offer TOP a license so that it could continue to engage in activities claimed by the patent, or that such a license, if made available to TOP, could be acquired on commercially acceptable terms. In addition, third parties may in the future, assert other intellectual property infringement claims against TOP with respect to its drug candidates, technologies or other matters.

TOP relies on confidentiality agreements that could be breached and may be difficult to enforce which could result in third parties using its intellectual property to compete against them.

TOP has taken and will continue to take reasonable steps to protect TOP’s intellectual property, including the use of agreements relating to the non-disclosure of confidential information to third parties, as well as agreements that purport to require the disclosure and assignment to TOP of the rights to the ideas, developments, discoveries and inventions of its employees and consultants while it employs them. These agreements may be difficult and costly to enforce. Although TOP has obtained and plans to continue to obtain these types of agreements from these third parties, to the extent that employees and consultants utilize or independently develop intellectual property in connection with any of TOP’s projects, disputes may arise as to the intellectual property rights associated with its drug candidates. If a dispute arises, a court may determine that the right belongs to a third party. Enforcement of TOP’s rights can be costly and unpredictable. Despite the protective measures TOP employs, TOP will still face the risk that:

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these agreements may be breached;

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these agreements may not provide adequate remedies for the applicable type of breach;

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TOP’s trade secrets or proprietary know-how will otherwise become known; or

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TOP’s competitors will independently develop similar technology or proprietary information.

Intellectual property rights may not necessarily address all potential threats to TOP’s competitive advantage.

The degree of future protection afforded by TOP’s intellectual property rights may be uncertain because intellectual property rights have limitations, and may not adequately protect TOP to enable it to maintain any competitive advantage. The following factors may weaken its protection:

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compounds or formulations may be made by others that are the same or similar to TOP’s drug candidates, but are not covered by TOP’s patent claims;

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inventions covered by TOP’s patents or pending patents may have been discovered by others previously;

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independently developed similar or alternative technologies may duplicate any of TOP’s proprietary assets without infringing TOP’s intellectual property rights;

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pending patents may not lead to issued patents;

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any patents issued in the future may not provide TOP with any competitive advantages, or may be held invalid or unenforceable as a result of legal challenges;

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TOP’s competitors might conduct research and development activities in the United States and other countries that provide a safe harbor from patent infringement claims for certain research and development activities, as well as in countries where TOP does not have patent rights; and

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the patents of others may have an adverse effect on TOP’s business.

TOP may become subject to litigation or regulatory action.

TOP may be named as a defendant in a lawsuit or regulatory action. TOP may also incur uninsured losses for liabilities which arise in the ordinary course of business, or which are unforeseen, including, but not limited to, employment liability and business loss claims. There is no assurance that shareholders will not lose their entire investment in TOP as a result of unforeseen litigation or regulatory action.

If TOP is unable to attract and retain key personnel, it may not be able to compete effectively in the cannabis market.

As of January 4, 2019, TOP has two full-time employees. TOP’s success will depend, in part, on its ability to attract and retain key scientific, management and other personnel. There is intense competition for qualified personnel in TOP’s area of activities, and TOP may not be able to attract and retain the qualified personnel necessary for the development of its business. In addition, TOP may have difficulty recruiting necessary personnel as a result of its limited operating history.

TOP will attempt to enhance its management, scientific and technical expertise by continuing to recruit qualified individuals who possess desired skills and experience in certain targeted areas and has entered into agreements with TOL to obtain the services of certain experienced scientific/technical personnel. TOP’s inability to retain employees and attract and retain sufficient additional employees or other scientific, engineering and technical support resources, could have a material adverse effect on TOP’s business, results of operations, financial condition and prospects.

TOP may suffer uninsured losses.

TOP does not currently have insurance coverage such as general liability, fire or other similar policies that may be customarily obtained for businesses similar to TOP, and any such event could cause significant losses for which no recovery would be available, and which could result in a material adverse impact on TOP’s business, results of operations, financial condition and prospects. Certain types of losses of a catastrophic nature, such as losses resulting from floods, tornadoes, thunderstorms, and earthquakes, are uninsurable or not economically insurable to the full extent of potential loss. Acts of God, work stoppages, regulatory actions or other causes, could adversely affect TOP’s business, operations, financial condition and prospects.

TOP may face adverse tax consequences.

The Internal Revenue Service and/or similar state and foreign government bodies may not accept the tax structure or tax positions taken by TOP. If TOP’s tax structure and/or tax positions are challenged or invalidated, any tax advantages contemplated by TOP with respect to TOP’s anticipated future profits or otherwise, may not be available, and this may result in adverse tax consequences to TOP and the holders of its securities.

Risks Related to Collaboration with Third Parties

Collaboration agreements that TOP has entered into and may enter into in the future may not be successful, which could adversely affect its ability to develop and commercialize cannabis-based products.

TOP has entered into and may enter into additional collaboration agreements with pharmaceutical companies or university, hospital, healthcare or biotechnology institutes or organizations in connection with the research, development or commercialization of its prospective cannabinoid-based products and treatments. TOP expects to face significant competition in seeking additional appropriate collaborators and

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in negotiating agreements on acceptable terms, and may not be successful in its efforts to enter into, implement and maintain collaboration agreements. Disagreements stemming from such collaboration agreements concerning development, intellectual property, regulatory or commercialization matters can lead to delays and, in some cases, termination of such collaboration agreements, or otherwise result in the potentially significant costs and fees in seeking to enforce or protect TOP’s rights, if any.

TOP will depend on third parties to conduct its research activities.

TOP has entered into agreements with third parties, such as medical institutions and clinical investigators, to design, conduct, supervise and monitor TOP’s pre-clinical studies and clinical trials (the “Third Parties”). TOP and the Third Parties are required to comply with various regulations and guidelines from regulatory authorities to ensure that the health, safety and rights of patients are protected in clinical development and clinical trials, and that trial data integrity is assured. Relying on Third Parties does not relieve TOP of certain responsibilities and requirements. If TOP or any of the Third Parties fail to comply with applicable requirements, the clinical data generated in such clinical trials may be deemed unreliable and the FDA, the EMA or other comparable foreign regulatory authorities may require TOP to perform additional clinical trials before approving its marketing applications. There is no assurance that upon inspection by a given regulatory authority, such regulatory authority will determine that any of TOP’s clinical trials comply with such requirements. Failure to comply with these regulations may require TOP to repeat preclinical studies and clinical trials, which would delay the regulatory approval process.

The Third Parties will not be employees of TOP. TOP therefore cannot control whether they devote sufficient time and resources to TOP’s ongoing pre-clinical and clinical programs. If the Third Parties do not successfully carry out their contractual duties or if the quality or accuracy of the clinical data they obtain is compromised due to their failure to adhere to clinical protocols and/or regulatory requirements, TOP’s clinical trials may be extended, delayed or terminated and TOP may not be able to obtain regulatory approval for, or successfully commercialize its drug candidates. As a result, TOP’s commercial prospects for its drug candidates would be harmed, its costs could increase and its ability to generate revenue could be delayed or reduced.

TOP has relied and intends to continue to rely upon Third Parties to formulate and produce its drug candidates in accordance with TOP’s clinical protocols and all applicable regulatory requirements, including, to the extent required, the FDA’s good clinical practice regulations and current good manufacturing practices and DEA and state regulations governing the handling, storage, security and recordkeeping for controlled substances, and corresponding regulations in other countries such as Israel. TOP also relies and intends to continue to rely on Third Parties to conduct and oversee its pre-clinical studies and clinical trials. These Third Parties have played and will continue to play a significant role in the formulation process and the development of TOP’s drug candidates. TOP intends to likely rely on these Third Parties for the formulation and development of the products to be utilized in its pre-clinical studies and clinical trials, and TOP will likely control minimally certain aspects of their activities. If these Third Parties do not meet TOP’s deadlines or otherwise conduct the trials as required, TOP may not be able to obtain regulatory approval for or commercialize its drug candidates when expected or at all.

If any of TOP’s clinical trial sites terminate their involvement in one of its clinical trials for any reason, TOP may experience the loss of follow-up information on patients enrolled in its ongoing clinical trials unless TOP is able to transfer the care of those patients to another qualified clinical trial site. In addition, principal investigators for TOP’s clinical trials may serve as scientific advisors or consultants to TOP from time to time and receive cash or equity compensation in connection with their services. If these relationships and any related compensation result in perceived or actual conflicts of interest, the integrity of the data generated at the applicable clinical trial site may be questioned by the FDA.

TOP conducts clinical trials for its drug candidates outside the United States and the FDA may not accept data from such trials.

TOP has conducted and continues to conduct clinical trials outside the United States, especially in Israel. Although the FDA may accept data from clinical trials conducted outside the United States, acceptance of such study data by the FDA is subject to certain conditions. For example, the study must be well designed and conducted and performed by qualified investigators in accordance with ethical principles.

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The study population must also adequately represent the U.S. population, and the data must be applicable to the U.S. population and U.S. medical practice in ways that the FDA deems clinically meaningful. Generally, the patient population for any clinical studies conducted outside of the United States must be representative of the population for whom TOP intends to label the product in the United States. In addition, such studies would be subject to the applicable local laws, and FDA acceptance of the data would be dependent upon its determination that the studies also complied with all applicable U.S. laws and regulations. There can be no assurance the FDA, the EMA or any comparable foreign agency will accept data from trials conducted outside of the United States, as much of the criteria is evaluated in the discretion of the FDA. Further, there is no assurance that the EMA or any comparable foreign agency will accept such data or otherwise satisfy or comply with the applicable requirements for preclinical studies and clinical trials in such jurisdictions. If the FDA, EMA or applicable foreign agency does not accept any such data or deems the data generated from any such preclinical studies or clinical trials as unreliable or insufficient, then it would likely result in the need for additional trials, which would be costly and time-consuming and delay aspects of TOP’s business plan.

Since TOP relies on Third Parties, TOP’s internal capacity to perform these functions will be limited. Outsourcing these functions involves risk that third parties may not perform to TOP’s standards, may not produce results in a timely manner or may fail to perform at all. In addition, the use of Third Parties requires TOP to disclose its proprietary information to these parties, which could increase the risk that this information will be misappropriated. Though TOP carefully manages its relationships with these Third Parties, there can be no assurance that challenges or delays in the future will not have a material adverse impact on the business, results of operations, financial condition and prospects of TOP.

Risks Relating to the Spin-Off and Merger

The proposed Spin-Off and Merger are contingent upon the satisfaction of a number of conditions, and the Spin-Off and Merger may not be consummated on the terms or timeline currently contemplated.

On November 5, 2018, our and Alliqua’s board of directors unanimously approved a plan to combine Alliqua’s custom hydrogels business with TOP’s business to form a separate, independent publicly traded company. For further discussion regarding aspects of the Spin-Off and Merger see “Summary — Questions and Answers about the Transaction”.

The consummation of the Merger is subject to certain conditions, including (i) the effectiveness of the registration statement to be filed with the SEC and the approval for listing on the Nasdaq Capital Market of the shares of AquaMed common stock to be issued in the Distribution, (ii) the accuracy of the parties’ representations and warranties and the performance of their respective covenants contained in the Merger Agreement, and (iii) consummation of the Private Placement. The consummation of the Spin-Off is subject to the foregoing conditions, plus certain additional conditions, including (i) the Adynxx Merger Agreement being in full force and effect and the Adynxx Merger being consummated immediately following with the Spin-Off and (ii) Alliqua being satisfied that the Spin-Off will not result in any material tax payable by Alliqua.

For these and other reasons, the Spin-Off and Merger may not be completed on the terms or timeline contemplated, if at all.

The proposed Spin-Off and Merger may result in disruptions to relationships with customers and other business partners or may not achieve the intended results.

If we complete the Spin-Off and Merger, there can be no assurance that we will be able to realize the intended benefits of the transactions or that the combined company will perform as anticipated. Specifically, the proposed transactions could cause disruptions in our business and the TOP business.

Further, it is possible that current or prospective employees of AquaMed or TOP could experience uncertainty about their future roles with the combined company, which could harm the ability of the combined company to attract and retain key personnel. Any of the foregoing could adversely affect our financial condition and results of operations and prospects.

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The actions required to implement the Spin-Off and Merger will take significant management time and attention and may require us to incur significant costs.

The Spin-Off and Merger will require significant amounts of management’s time and resources, which will be in addition to and may divert management’s time and attention from the operation of our business and the execution of our other strategic initiatives. Additionally, we may incur significant costs in connection with the Spin-Off and Merger. The Merger Agreement contains certain termination rights for us and TOP.

The Spin-Off is a taxable transaction and Alliqua and its stockholders may be subject to a tax liability in connection with the Distribution.

For U.S. federal income tax purposes, the distribution by Alliqua of the shares of AquaMed common stock will not be eligible for treatment as a tax-free distribution. Accordingly, each holder of Alliqua common stock who receives shares of AquaMed common stock in the Spin-Off generally will be treated as if such stockholder received a taxable distribution in an amount equal to the fair market value of AquaMed common stock received (including any fractional share deemed to be received by and sold on behalf of the stockholder), which will result in: (a) a dividend to the extent of such stockholder’s ratable share of Alliqua’s current and accumulated earnings and profits; then (b) a reduction in such stockholder’s basis in Alliqua’s common stock (but not below zero) to the extent the amount received exceeds the amount referenced in clause (a); and then (c) gain from the sale or exchange of Alliqua common stock to the extent the amount received exceeds the sum of the amounts referenced in clauses (a) and (b). Accordingly, the amount of taxable income realized by each Alliqua stockholder in the Spin-Off may depend upon its basis in its Alliqua stock, but such tax liability may be significant.

In addition, a corporate level U.S. federal income tax will be payable by the consolidated group of which Alliqua is the common parent if gain realized in the Spin-Off exceeds any net operating losses that may be available to offset such gain. The tax would be based upon the gain, if any, computed as the difference between the fair market value of the AquaMed common stock and Alliqua’s adjusted basis in such stock. Alliqua expects that it will have sufficient losses available to fully offset any gain realized as a result of the Spin-Off.

After the Spin-Off, one of our directors and officers may have actual or potential conflicts of interest because of his previous or continuing positions at Alliqua.

Because of his current or former positions with Alliqua, our expected chairman of the board will own Alliqua common stock and equity awards. Following the Spin-Off, even though our Board of Directors will consist of a majority of directors who are independent, our chairman of the board will continue to have a financial interest in Alliqua common stock and equity awards. Continuing ownership of Alliqua common stock and equity awards, or service as a director at both companies could create, or appear to create, potential conflicts of interest if we have disagreements with Alliqua about the contracts between us that continue or face decisions that could have different implications for us and Alliqua.

We may be unable to achieve some or all of the benefits that we expect to achieve from the Spin-Off.

We believe that, as an independent publicly-traded company, we will be able to, among other things, better focus our financial and operational resources on our specific business, implement and maintain a capital structure designed to meet our specific needs, design and implement corporate strategies and policies that are targeted to our business, more effectively respond to industry dynamics and create effective incentives for our management and employees that are more closely tied to our business performance. However, by separating from Alliqua, we may be more susceptible to market fluctuations and other adverse events. In addition, we may be unable to achieve some or all of the benefits that we expect to achieve as an independent company in the time we expect, if at all. If we fail to achieve some or all of the benefits that we expect to achieve as an independent company, or do not achieve them in the time we expect, our business, financial condition, results of operations and prospects could be adversely affected.

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We may be unable to make, on a timely or cost-effective basis, the changes necessary to operate as an independent publicly-traded company, and we may experience increased costs after the Spin-Off.

We have historically operated as part of Alliqua’s corporate organization, and Alliqua has provided us with various corporate functions. Following the Spin-Off, Alliqua will have no obligation to provide us with assistance other than limited transition services pursuant to the Asset Contribution and Separation Agreement between us and Alliqua. These services do not include every service that we have received from Alliqua in the past. Accordingly, following the Spin-Off, we will need to provide internally or obtain from unaffiliated third parties the services we currently receive from Alliqua. These services include IT, tax administration, treasury activities, technical accounting, benefits administration, procurement, legal and ethics and compliance program administration, the effective and appropriate performance of which are critical to our operations. We may be unable to replace these services in a timely manner or on terms and conditions as favorable as those we receive from Alliqua.

We have no recent operating history as an independent publicly-traded company, and our historical financial information is not necessarily representative of the results we would have achieved as an independent publicly traded company and may not be a reliable indicator of our future results.

We derived our historical financial information included in this prospectus from Alliqua’s combined and consolidated financial statements, and this information does not necessarily reflect the results of operations and financial positions we would have achieved as an independent publicly-traded company during the periods presented, or those that we will achieve in the future. This is primarily because of the following factors:

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Prior to the Spin-Off, we operated as part of Alliqua’s broader corporate organization and Alliqua performed various corporate functions for us, including IT, tax administration, treasury activities, technical accounting, benefits administration, procurement, legal and ethics and compliance program administration. Our historical financial information reflects allocations of corporate expenses from Alliqua for these and similar functions. These allocations may not reflect the costs we will incur for similar services in the future as an independent publicly-traded company.

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Our historical financial information does not reflect changes that we expect to experience in the future as a result of our separation from Alliqua, including changes in our cost structure, personnel needs, tax profile, financing and business operations. As part of Alliqua, we enjoyed certain benefits from Alliqua’s operating diversity, size, purchasing power, borrowing leverage and available capital for investments, and we will lose these benefits after the Spin-Off. As an independent entity, we may be unable to purchase goods, services and technologies, such as insurance and health care benefits and computer software licenses, or access capital markets on terms as favorable to us as those we obtained as part of Alliqua prior to the Spin-Off.

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The Merger will result in our consolidated operations and the results therefrom being substantially different than Alliqua’s operations and the results therefrom and as a result, our historical information will not necessarily reflect our results of operations going forward.

Following the Spin-Off, we will also be responsible for the additional costs associated with being an independent publicly-traded company, including costs related to corporate governance, investor and public relations and public reporting. Therefore, our financial statements may not be indicative of our future performance as an independent publicly-traded company. For additional information about our past financial performance and the basis of presentation of our financial statements, see “Selected Historical Financial Data for AquaMed,” “Management’s Discussion and Analysis of Financial Condition and Results of Operations of AquaMed” and our historical financial statements and the notes thereto included elsewhere in this prospectus.

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Our and TOP’s historical and pro forma financial data are not necessarily representative of the results the combined company would have achieved and may not be a reliable indicator of the combined company’s future results.

Our and TOP’s historical and pro forma financial data included in this prospectus may not reflect what our or TOP’s results of operations and financial position would have been had we been a combined company, and publicly traded, during the periods presented, or what the combined company’s results of operations, financial condition and cash flows will be in the future. In addition, the pro forma financial data we have included in this prospectus are based in part upon a number of estimates and assumptions. These estimates and assumptions may prove not to be accurate, and accordingly, our pro forma financial data should not be assumed to be indicative of what our financial condition or results of operations actually would have been as a combined company and may not be a reliable indicator of what our financial condition or results of operations actually may be in the future.

Some of the contracts to be transferred or assigned to us contain provisions requiring the consent of third parties in connection with the transactions contemplated by the Internal Reorganization and Distribution. If these consents are not obtained, we may be unable to enjoy the benefit of these contracts in the future.

Some of the contracts to be transferred or assigned to us in connection with the Internal Reorganization and Distribution contain provisions that require the consent of third parties to the Internal Reorganization, the Distribution or both. Failure to obtain such consents on commercially reasonable and satisfactory terms may impair our entitlement to the benefit of these contracts in the future.

Our potential indemnification liabilities pursuant to the Asset Contribution and Separation Agreement could materially and adversely affect us.

The Asset Contribution and Separation Agreement between us and Alliqua will provide for, among other things, the principal corporate transactions required to effectuate the Spin-Off, certain conditions to the Spin-Off and provisions governing the relationship between us and Alliqua after the Spin-Off. For a description of the Asset Contribution and Separation Agreement, see “The Asset Contribution and Separation Agreement and Ancillary Agreements — Separation Agreement.” Among other things, the Asset Contribution and Separation Agreement will provide for indemnification obligations designed to make us financially responsible for substantially all liabilities that may exist relating to or arising out of our business. If we are required to indemnify Alliqua under the circumstances set forth in the Asset Contribution and Separation Agreement, we may be subject to substantial liabilities.

In connection with the Spin-Off, Alliqua will indemnify us for certain liabilities. However, there can be no assurance that these indemnities will be sufficient to insure us against the full amount of such liabilities, or that Alliqua’s ability to satisfy its indemnification obligation will not be impaired in the future.

Pursuant to the Asset Contribution and Separation Agreement and other agreements we will enter into in connection with the Spin-Off, Alliqua will agree to indemnify us for certain liabilities. However, third parties could seek to hold us responsible for any of the liabilities that Alliqua will agree to retain pursuant to these agreements, and there can be no assurance that Alliqua will be able to fully satisfy its indemnification obligations under these agreements. Moreover, even if we ultimately succeed in recovering from Alliqua any amounts for which we are held liable, we may be temporarily required to bear these losses while seeking recovery from Alliqua.

The Distribution may not be completed on the terms or timeline currently contemplated, if at all.

We are actively engaged in planning for the Distribution. We expect to incur expenses in connection with the Distribution and any delays in the anticipated completion of the distribution may increase these expenses. Unanticipated developments could delay or negatively impact the distribution, including those related to the filing and effectiveness of appropriate filings with the SEC, the listing of our common stock on the Nasdaq Capital Market, and receiving any required regulatory approvals. Until the consummation of the Distribution, Alliqua’s Board of Directors will have the sole and absolute discretion to determine and change the terms of the Distribution, including the establishment of the record date and distribution date.

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Risks Relating to our Common Stock and Capital Structure

No market for our common stock currently exists and an active trading market may not develop or be sustained after the Spin-Off. Following the Spin-Off our stock price may fluctuate significantly.

There is currently no public market for our common stock. We intend to apply to list our common stock on the Nasdaq Capital Market. However, an active trading market for our common stock may not develop as a result of the Spin-Off or may not be sustained in the future. The lack of an active market may make it more difficult for stockholders to sell our shares and could lead to our share price being depressed or volatile.

We cannot predict the prices at which our common stock may trade after the Spin-Off. The market price of our common stock may fluctuate widely, depending on many factors, some of which may be beyond our control, including:

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actual or anticipated fluctuations in our operating results due to factors related to our business;

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success or failure of our business strategies;

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our quarterly or annual earnings, or those of other companies in our industry;

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our ability to obtain financing as needed;

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announcements by us or our competitors of significant acquisitions or dispositions;

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changes in accounting standards, policies, guidance, interpretations or principles;

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the failure of securities analysts to cover our common stock after the Spin-Off;

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changes in earnings estimates by securities analysts or our ability to meet those estimates;

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the operating and stock price performance of other comparable companies;

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overall market fluctuations;

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results from any material litigation or government investigation;

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changes in laws and regulations (including tax laws and regulations) affecting our business;

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changes in capital gains taxes and taxes on dividends affecting stockholders; and

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general economic conditions and other external factors.

Furthermore, our business profile and market capitalization may not fit the investment objectives of some Alliqua stockholders and, as a result, these Alliqua stockholders may sell their shares of our common stock after the Distribution. Substantial sales of our common stock may occur in connection with the Spin-Off, which could cause our stock price to decline. Low trading volume for our stock, which may occur if an active trading market does not develop, among other reasons, would amplify the effect of the above factors on our stock price volatility.

Substantial sales of our common stock may occur in connection with the Spin-Off, which could cause our stock price to decline.

Although we have no actual knowledge of any plan or intention of any significant Alliqua and TOP stockholder to sell our common stock following the Spin-Off, it is likely that some such stockholders, possibly including some larger stockholders, will sell their shares of our common stock received in the Distribution or the Merger if, for reasons such as our business profile or market capitalization as an independent company, we do not fit their investment objectives or, in the case of index funds, we are not a participant in the index in which they are investing. Following the Merger, approximately 38% of our outstanding shares of common stock will be beneficially owned by our five largest stockholders, including Berel Farkas (who is also a director), who would be expected to exercise substantial influence on any matters subject to a stockholder vote. These shares will also be eligible for resale in the public market

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without registration subject to volume, manner of sale and holding period limitations under Rule 144 under the Securities Act commencing 90 days after the date of this prospectus. The sales of significant amounts of our common stock or the perception in the market that this will occur may decrease the market price of our common stock.

The combined post-Spin-Off value of Alliqua common stock and our common stock may not equal or exceed the pre-Spin-Off value of Alliqua common stock.

We cannot assure you that the combined trading prices of Alliqua common stock and our common stock after the Spin-Off will be equal to or greater than the trading price of Alliqua common stock prior to the Spin-Off. Until the market has fully evaluated the business of Alliqua without our business, the price at which Alliqua common stock trades may fluctuate more significantly than might otherwise be typical. Similarly, until the market has fully evaluated the stand-alone business of our company, the price at which shares of our common stock trades may fluctuate more significantly than might otherwise be typical, including volatility caused by general market conditions.

We cannot assure you that we will pay dividends on our common stock, and our indebtedness may limit our ability to pay dividends on our common stock.

Following the Spin-Off, the timing, declaration, amount and payment of future dividends to stockholders will fall within the discretion of our Board of Directors. Our Board of Directors’ decisions regarding the payment of future dividends will depend on many factors, including our financial condition, earnings, capital requirements of our business and covenants associated with debt obligations, as well as legal requirements, regulatory constraints, industry practice and other factors that our Board of Directors deems relevant. For more information, see “Dividend Policy.” There can be no assurance that we will pay a dividend in the future or continue to pay any dividend if we do commence paying dividends, and there can be no assurance that, in the future, the combined annual dividends paid on Alliqua common stock, if any, and our common stock, if any, after the Spin-Off will equal the annual dividends on Alliqua common stock prior to the Spin-Off.

Your percentage ownership in us may be diluted in the future.

Your percentage ownership in us may be diluted in the future because of equity awards that we expect to grant to our directors, officers and other employees. Prior to completion of the Spin-Off, we expect to approve an incentive plan that will provide for the grant of common share-based equity awards to our directors, officers and other employees. In addition, we may issue equity as all or part of the consideration paid for acquisitions and strategic investments that we may make in the future or as necessary to finance our ongoing operations.

We are an “emerging growth company” and a “smaller reporting company” and may elect to comply with reduced public company reporting requirements applicable to emerging growth companies, and are subject to lesser public company reporting requirements applicable to smaller reporting companies, which could make our common stock less attractive to investors.

We are an “emerging growth company,” as defined in the JOBS Act, and we may take advantage of certain exemptions from various reporting requirements that are applicable to other public companies that are not “emerging growth companies” including reduced disclosure obligations regarding executive compensation in our periodic reports and proxy statements, and exemptions from the requirements of holding a nonbinding advisory vote on executive compensation and shareholder approval of any golden parachute payments not previously approved. We may take advantage of these reporting exemptions until we are no longer an “emerging growth company.” We will remain an “emerging growth company” until the earliest of (i) the last day of the fiscal year in which we have total annual gross revenues of $1.07 billion or more; (ii) the fifth anniversary of the Distribution; (iii) the date on which we have issued more than $1.0 billion in nonconvertible debt during the previous three years; or (iv) the date on which we are deemed to be a “large accelerated filer” under the Exchange Act. We cannot predict if investors will find our common stock less attractive because we may rely on these exemptions. In addition, we are a “smaller reporting company” and accordingly are required to provide less public disclosure than larger public companies. If some investors find our common stock less attractive as a result, there may be a less active trading market for our common stock and our stock price may be more volatile.

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We will incur costs as a result of operating as a public company, and our management will be required to devote substantial time to new compliance initiatives.

As a public reporting company, and particularly after we are no longer an emerging growth company, we will incur significant legal, accounting and other expenses. The Sarbanes-Oxley Act and rules subsequently implemented by the SEC, have imposed various requirements on public companies, including establishment and maintenance of effective disclosure and financial controls and corporate governance practices. Our management and other personnel will need to devote a substantial amount of time to these compliance initiatives. Moreover, these rules and regulations will entail significant legal and financial compliance costs and will make some activities more time consuming and costly. For example, we expect that these rules and regulations may make it difficult and expensive for us to obtain director and officer liability insurance, and we may be required to accept low policy limits and coverage.

Provisions in our Amended and Restated Certificate of Incorporation and Amended and Restated Bylaws and of Delaware law may prevent or delay an acquisition of our company, which could decrease the trading price of our common stock.

Several provisions of our Amended and Restated Certificate of Incorporation, Amended and Restated Bylaws and Delaware law may discourage, delay or prevent a merger or acquisition that stockholders may consider favorable. These include provisions that:

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permit us to issue blank check preferred stock as more fully described under “Description of Our Capital Stock Anti-Takeover Effects of Various Provisions of Delaware Law and Our Amended and Restated Articles of Incorporation and Amended and Restated Bylaws”;

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require stockholders to follow certain advance notice and disclosure requirements in order to propose business or nominate directors at an annual or special meeting; and

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limit our ability to enter into business combination transactions with certain stockholders.

These and other provisions of our Amended and Restated Certificate of Incorporation, Amended and Restated Bylaws and Delaware law may discourage, delay or prevent certain types of transactions involving an actual or a threatened acquisition or change in control of us, including unsolicited takeover attempts, even though the transaction may offer our stockholders the opportunity to sell their shares of our common stock at a price above the prevailing market price. See “Description of Our Capital Stock Anti-Takeover Effects of Various Provisions of Delaware Law and Our Amended and Restated Articles of Incorporation and Amended and Restated Bylaws” for more information.

Our Amended and Restated Bylaws include a forum selection clause, which could limit our stockholders’ ability to obtain a favorable judicial forum for disputes with us.

Our Amended and Restated Bylaws provide that, unless we consent in writing to the selection of an alternative forum, the sole and exclusive forum for (i) any internal corporate claims within the meaning of the Delaware General Corporation Law (“DGCL”), (ii) any derivative action or proceeding brought on our behalf, (iii) any action asserting a claim of breach of a fiduciary duty owed by any of our directors, officers, or employees to us or to our stockholders, or (iv) any action asserting a claim arising pursuant to any provision of the DGCL, will be a state or federal court located within the State of Delaware, in all cases subject to the court’s having personal jurisdiction over the indispensable parties named as defendants. Any person or entity purchasing or otherwise acquiring any interest in shares of our capital stock is deemed to have notice of and consented to the foregoing provisions. This forum selection provision in our bylaws may limit our stockholders’ ability to obtain a favorable judicial forum for disputes with us. It is also possible that, notwithstanding the forum selection clause included in our bylaws, a court could rule that such a provision is inapplicable or unenforceable.

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CAUTIONARY STATEMENT CONCERNING FORWARD-LOOKING STATEMENTS

All statements and assumptions contained in this prospectus that do not directly and exclusively relate to historical facts constitute “forward-looking statements.” Forward-looking statements often include words such as “anticipates,” “believes,” “estimates,” “expects,” “forecast,” “goal,” “intends,” “objective,” “plans,” “projects,” “strategy,” “target,” and “will” and words and terms of similar substance in discussions of future operating or financial performance. These statements represent current expectations and beliefs, and no assurance can be given that the results described in such statements will be achieved

Forward-looking statements include, among other things, statements with respect to our financial condition, results of operations, cash flows, business strategies, prospects, operating efficiencies or synergies, competitive position, growth opportunities, plans and objectives of management and other matters. Such statements are subject to numerous assumptions, risks, uncertainties and other factors that could cause actual results to differ materially from those described in such statements, many of which are outside of our control. Important factors that could cause actual results to differ materially from those described in forward-looking statements include, but are not limited to:

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the inability or failure to perform under the various transaction agreements effecting the Spin-Off or the Merger;

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the ability to realize the benefits expected to result from the Merger within the anticipated time frame or in the anticipated amounts;

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other risks related to the Spin-Off and the Merger, including anticipated tax treatment, unforeseen liabilities, and future capital expenditures;

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the occurrence of any event, change or other circumstances that could give rise to the termination of the Adynxx Merger Agreement;

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Alliqua’s stockholders failing to approve the Adynxx Merger;

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risks arising from the diversion of management’s attention from our ongoing business operations;

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inadequate or an inability to raise sufficient capital to execute our business plan;

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any inability to successfully develop drug candidates, obtain regulatory approval and achieve market acceptance thereof;

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failure to design and achieve successful results in pre-clinical and clinical trials for our prospective drug candidates;

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our ability to comply with current good manufacturing practices;

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loss or retirement of key executives;

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adverse economic conditions and/or intense competition;

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loss of a key customer or supplier;

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entry of new competitors;

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adverse federal, state and local government regulation;

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technological obsolescence of our manufacturing process and equipment;

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technical problems with our research and products;

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price increases for supplies and components; and

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the inability to carry out our business plans

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There may be other factors that may cause our actual results to differ materially from the forward-looking statements, including factors disclosed under the sections titled “Risk Factors”, “Management’s Discussion and Analysis of Financial Condition and Results of Operations of AquaMed” and “Management’s Discussion and Analysis of Financial Condition and Plan of Operations of TOP” in this prospectus. You should evaluate all forward-looking statements made in this prospectus in the context of these risks and uncertainties.

No assurance can be given that any goal or plan set forth in any forward-looking statement can or will be achieved, and readers are cautioned not to place undue reliance on such statements which speak only as of the date they are made. We do not undertake any obligation to update or release any revisions to any forward-looking statement or to report any events or circumstances after the date of this prospectus or to reflect the occurrence of unanticipated events, except as required by law.

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THE TRANSACTIONS

Background

On November 28, 2018, Alliqua announced plans for the complete legal and structural separation of its custom hydrogels contract manufacturing business and the subsequent combination of AquaMed and TOP to create a new public bio-pharmaceutical company focused on discovering, developing and commercializing novel therapeutics based on TOP’s proprietary cannabinoid product platform in a number of FDA-regulated clinical indications.

See also “Reasons for the Spin-Off and Merger — Spin-Off”.

To effectuate the separation, Alliqua is undertaking the Internal Reorganization described under “The Asset Contribution and Separation Agreement and Ancillary Agreements.”

Following the Spin-Off, Alliqua will not own any equity interest in us, and we will operate independently from Alliqua. No approval of Alliqua’s stockholders is required in connection with the Spin-Off, and Alliqua’s stockholders will not have any appraisal rights in connection with the Spin-Off.

Completion of the Spin-Off is subject to the satisfaction, or the waiver of the board of directors of Alliqua, of a number of conditions. For a more detailed description, see “Conditions to the Spin-Off.”

Following the Spin-Off, under the Merger Agreement and in accordance with Delaware law, Merger Sub will merge with and into TOP, with TOP continuing as the surviving company. As a result of the Merger, TOP will become a wholly-owned subsidiary of us. As a result of the Merger, immediately after the effective time of the Merger and consummation of the Private Placement, before giving effect to any fees payable in equity to financial advisors or other intermediaries, the current members of TOP and the third-party investors that participate in the Private Placement are expected to hold approximately 90% of the total number of shares of AquaMed common stock outstanding (on a fully diluted basis), assuming that no more than $10 million is raised in the Private Placement. For details of the structure of the transaction, see “The Merger Agreement.”

Reasons for the Spin-Off and Merger

The board of directors of Alliqua regularly conducts strategic reviews of its businesses. In reaching the decision to pursue the Spin-Off and Merger, the board of directors of Alliqua considered a range of potential strategic alternatives for Alliqua, including the continuation of Alliqua’s current operating strategy in light of the Adynxx Merger as well as potential acquisition and divestiture transactions. In evaluating these alternatives, the board of directors of Alliqua considered a number of factors, including (a) the relative values to Alliqua’s stockholders of (i) AquaMed operating as an independent business versus (ii) continuing with the combined Alliqua/Adynxx business, (b) the strategic focus and flexibility for Alliqua and AquaMed after the Spin-Off and Merger, (c) the ability of Alliqua and AquaMed to operate efficiently and effectively (including AquaMed’s ability to retain and attract management talent) after the Spin-Off and Merger, (d) the financial profile of Alliqua, AquaMed and TOP, (e) the potential reaction of customers, employees and investors and (f) the probability of successful execution of the various strategic alternatives and the risks associated with those alternatives.

As a result of this evaluation, the board of directors of Alliqua determined that proceeding with the Spin-Off and the Merger would be in the best interests of Alliqua and its stockholders. The board of directors of Alliqua considered the following potential benefits of this approach:

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custom hydrogels business. We believe the Spin-Off and the Merger will provide greater value to Alliqua stockholders than if the AquaMed business remained a part of Alliqua following the closing of the Adynxx Merger as the combination of AquaMed and TOP will create an independent, publicly traded company dedicated to discovering, developing and commercializing novel therapeutics based on TOP’s proprietary cannabinoid product platform and serving customers in the cannabinoid pharmaceutical therapy industry.

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Strategic Focus and Flexibility. Following the Spin-Off and Merger, we will be better able to dedicate financial and human capital resources to pursue appropriate growth opportunities and execute strategic plans best suited to our business than if it remained a part of Alliqua or as an independent company without the business combination with TOP.

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Strategic Positioning in Industry. The combination of AquaMed and TOP is a strategic move to position the combined company as an independent, publicly traded cannabinoid pharmaceutical therapy-based company. The combination of AquaMed and TOP is expected to provide opportunities for the combined company to leverage its unique ability to create novel therapeutics based on TOP’s proprietary cannabinoid-based product platform in a number of FDA-regulated clinical indications, including a hydrogel product.

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In determining whether to effect the Spin-Off, the board of directors of Alliqua considered the costs and risks associated with the Spin-Off, including the costs associated with preparing AquaMed to become an independent, publicly-traded company, the risk of volatility in our stock price immediately following the Spin-Off due to sales by Alliqua’s stockholders whose investment objectives may not be met by our common stock, the time it may take for us to attract our optimal stockholder base, the possibility of disruptions in our business as a result of the Spin-Off, the risk that the combined trading prices of our common stock and Alliqua’s common stock after the Spin-Off may drop below the trading price of Alliqua’s common stock before the Spin-Off and the loss of synergies and scale from operating as one company. Notwithstanding these costs and risks, taking into account the factors discussed above, the board of directors of Alliqua determined that the Spin-Off was the best alternative to achieve the above benefits and enhance stockholder value.

In assessing and approving the Merger, Alliqua considered that the expected value to Alliqua and its stockholders from pursuing the Merger was greater than the value to Alliqua and its stockholders of the stand-alone Spin-Off. In addition to the factors noted above, Alliqua considered TOP’s business and prospects, after giving effect to the proposed acquisition by us, including expected synergies to be realized as a result of the Merger. The board of directors of Alliqua also considered the potential risks and countervailing factors associated with the Merger, including that the anticipated benefits of the Merger might not be realized. After consideration of the above factors and based on information furnished by TOP to Alliqua and the terms of the Merger Agreement and related agreements as finally negotiated by Alliqua, Alliqua concluded that the expected value to Alliqua and its stockholders from pursuing the Transactions was greater than the value to Alliqua and its stockholders of the stand-alone Spin-Off.

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When and How You Will Receive AquaMed Shares

Alliqua will distribute to its stockholders, as a pro rata dividend, shares of our common stock for every one share of Alliqua common stock outstanding as of , the Record Date of the Distribution.

Prior to the Spin-Off, Alliqua will deliver all of the issued and outstanding shares of our common stock to the distribution agent. Action Stock Transfer Corporation will serve as distribution agent in connection with the Distribution and as transfer agent and registrar for our common stock.

If you own Alliqua common stock as of the close of business on , 2019, the shares of our common stock that you are entitled to receive in the Distribution will be issued to your account as follows:

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Commencing on or shortly after the Distribution Date, the distribution agent will mail to you an account statement that indicates the number of shares of our common stock that have been registered in book-entry form in your name. We expect it will take the distribution agent up to two weeks after the Distribution Date to complete the distribution of the shares of our common stock and mail statements of holding to all registered stockholders. Trading of our common stock will not be affected by this delay in issuance by the distribution agent.

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“Street name” or beneficial stockholders. Most Alliqua stockholders own their shares of Alliqua common stock beneficially through a bank, broker or other nominee. In these cases, the bank, broker or other nominee holds the shares in “street name” and records your ownership on its books. If you own your shares of Alliqua common stock through a bank, broker or other nominee, your bank, broker or other nominee will credit your account with the shares of our common stock that you receive in the Distribution on or shortly after the Distribution Date. We encourage you to contact your bank, broker or other nominee if you have any questions concerning the mechanics of having shares held in “street name.”

If you sell any of your shares of Alliqua common stock on or before the Distribution Date, the buyer of those shares may in some circumstances be entitled to receive the shares of our common stock to be distributed in respect of the Alliqua shares you sold. We anticipate that, on or shortly before the Record Date and continuing up to and including the Distribution Date, there will be two markets in Alliqua common stock: a “regular-way” market and an “ex-dividend” market. Shares of Alliqua common stock that trade on the “regular-way market” will trade with the entitlement to receive shares of our common stock in the Distribution. Shares that trade on the ex-dividend market will trade without the entitlement to receive shares of our common stock in the Distribution. Therefore, if you sell shares of Alliqua common stock in the “regular-way” market up to and including the Distribution Date, you will be selling your right to receive shares of our common stock in the Distribution. If you hold shares of Alliqua common stock on the Record Date and then decide to sell any shares of Alliqua common stock before the Distribution Date, you should make sure your stockbroker, bank or other nominee understands whether you want to sell your shares of Alliqua common stock with or without your entitlement to our common stock pursuant to the Distribution.

We are not asking Alliqua stockholders to take any action in connection with the Spin-Off. No stockholder approval of the Spin-Off is required. We are not asking you for a proxy and request that you do not send us a proxy.

We are also not asking you to make any payment or surrender or exchange any of your shares of Alliqua common stock for shares of our common stock. The number of outstanding shares of Alliqua common stock will not change as a result of the Spin-Off.

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Number of Shares You Will Receive

On the Distribution Date, we will distribute shares of our common stock for every one share of Alliqua common stock.

Treatment of Fractional Shares

The distribution agent will not distribute any fractional shares of our common stock in connection with the Distribution. Instead, the distribution agent will aggregate all fractional shares into whole shares and sell the whole shares in the open market at prevailing market prices on behalf of Alliqua stockholders entitled to receive a fractional share. The distribution agent will then distribute the aggregate cash proceeds of the sales, net of brokerage fees and other costs, pro rata to these holders (net of any required withholding for taxes applicable to each holder). The distribution agent will, in its sole discretion, without any influence by Alliqua or us, determine when, how, through which broker-dealer and at what price to sell the whole shares. The distribution agent is not, and any broker-dealer used by the distribution agent will not be, an affiliate of either Alliqua or us.

The distribution agent will send to each registered holder of Alliqua common stock entitled to a fractional share a check in the cash amount deliverable in lieu of that holder’s fractional share as soon as practicable following the Distribution. We expect the distribution agent to take about two weeks after the Distribution to complete the distribution of cash in lieu of fractional shares to Alliqua stockholders. If you hold your shares through a bank, broker or other nominee, your bank, broker or nominee will receive, on your behalf, your pro rata share of the aggregate net cash proceeds of the sales. No interest will be paid on any cash you receive in lieu of a fractional share. The cash you receive in lieu of a fractional share will generally be taxable to you for U.S. federal income tax purposes. See “Material U.S. Federal Income Tax Consequences of the Distribution” below for more information.

Results of the Spin-Off

After the Spin-Off, we will be an independent publicly-traded company. Immediately following the Spin-Off, we expect to have approximately registered holders of shares of our common stock and approximately shares of our common stock outstanding. The actual number of shares of our common stock you will receive in the Spin-Off will depend on the actual number of shares of Alliqua common stock outstanding on the Record Date, which will reflect any issuance of new shares or exercises of outstanding options pursuant to Alliqua’s equity plans, and any repurchase of Alliqua shares by Alliqua under its common stock repurchase program, on or prior to the Record Date. The Spin-Off will not affect the number of outstanding shares of Alliqua common stock or any rights of Alliqua stockholders, although we expect the trading price of shares of Alliqua common stock immediately following the Distribution to be lower than immediately prior to the Distribution because the trading price of Alliqua common stock will no longer reflect the value of the AquaMed business. Furthermore, until the market has fully analyzed the value of Alliqua without the AquaMed business, the trading price of shares of Alliqua common stock may fluctuate.

Before our separation from Alliqua, we intend to enter into an Asset Contribution and Separation Agreement and several other agreements with Alliqua related to the Spin-Off. These agreements will govern the relationship between AquaMed and Alliqua up to and after completion of the Spin-Off and allocate between AquaMed and Alliqua various assets, liabilities, rights and obligations, including employee benefits and tax-related assets and liabilities. We describe these arrangements in greater detail under “The Asset Contribution and Separation Agreement and Ancillary Agreements” and “Certain Relationships and Related Party Transactions — Agreements with Alliqua.”

Listing and Trading of Our Common Stock

As of the date of this prospectus, we are a wholly owned subsidiary of Alliqua. Accordingly, no public market for our common stock currently exists. We intend to list our shares of common stock on the Nasdaq Capital Market under the symbol “TOPP.” Following the Spin-Off, Alliqua common stock will continue to trade on the Nasdaq Capital Market under the symbol “ALQA.”

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Neither we nor Alliqua can assure you as to the trading price of Alliqua common stock or our common stock after the Spin-Off, or as to whether the combined trading prices of our common stock and Alliqua common stock after the Spin-Off will be less than, equal to or greater than the “regular-way” trading price of Alliqua common stock prior to the Spin-Off. The trading price of our common stock may fluctuate significantly following the Spin-Off. See “Risk Factors — Risks Relating to Our Common Stock and the Securities Market” for more detail.

The shares of our common stock distributed to Alliqua stockholders will be freely transferable, except for shares received by individuals who are our affiliates. Individuals who may be considered our affiliates after the Spin-Off include individuals who control, are controlled by or are under common control with us, as those terms generally are interpreted for federal securities law purposes. These individuals may include some or all of our directors and executive officers. Individuals who are our affiliates will be permitted to sell their shares of our common stock only pursuant to an effective registration statement under the Securities Act of 1933, as amended (“Securities Act”) or an exemption from the registration requirements of the Securities Act, such as those afforded by Section 4(a)(1) of the Securities Act or Rule 144 thereunder.

Conditions to the Spin-Off

We expect that the separation will be effective on the Distribution Date, provided that the following conditions, in addition to other customary closing conditions, shall have been satisfied or waived by Alliqua:

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the board of directors of Alliqua shall have approved the Internal Reorganization and the Distribution and shall have declared the Distribution of AquaMed common stock to Alliqua stockholders;

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the ancillary agreements contemplated by the Asset Contribution and Separation Agreement shall have been executed by each party to those agreements;

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the SEC shall have declared effective our Registration Statement on Form S-1, of which this prospectus is a part, under the Exchange Act, and no stop order suspending the effectiveness of the Registration Statement shall be in effect and no proceedings for that purpose shall be pending before or threatened by the SEC;

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our common stock shall have been accepted for listing on the Nasdaq Capital Market, subject to official notice of issuance;

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we shall have concurrently consummated the Private Placement;

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the Merger Agreement shall be in full force and effect;

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Alliqua shall have received an independent third-party valuation of our common stock to be distributed in the Distribution;

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Alliqua shall be satisfied the Internal Reorganization and the Distribution, will not result in any material tax payable by Alliqua;

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the Adynxx Merger Agreement, shall be in full force and effect and the transactions contemplated thereby shall be consummated immediately following the closing of the Spin-Off; and

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no proceeding shall be pending or threatened in writing seeking to enjoin, delay, prohibit or restrict the consummation of the Spin-Off or the Merger.

The fulfillment of the above conditions will not create any obligation on Alliqua’s part to effect the Spin-Off. We are not aware of any material federal, foreign or state regulatory requirements with which we must comply, other than SEC rules and regulations, or any material approvals that we must obtain, other than the approval for listing of our common stock and the SEC’s declaration of the effectiveness of the Registration Statement, in connection with the Distribution.

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Conditions to Consummation of the Merger

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the Spin-Off having occurred pursuant to the Asset Contribution and Separation Agreement;

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the absence of any order issued by any governmental authority of competent jurisdiction or other legal impediment preventing or making illegal the consummation of the Merger; and

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we shall have received binding commitments from investors to consummate the Private Placement.

In addition, our, and Merger Sub’s obligations to consummate the Merger are subject to the satisfaction or waiver (to the extent permitted by applicable law) of the following conditions:

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the covenants and agreements being performed by TOP in all material respects at or prior to the effective time of the Merger;

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TOP shall have obtained the consent of its sole member, and such consent shall not have been invalidated or revoked and shall remain in full force and effect;

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the absence of a TOP Material Adverse Effect since the date of the Merger Agreement;

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TOP shall have completed an audit of its financial statements for the years ended December 31, 2017 and December 31, 2016 by an independent registered auditor; and

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we shall have received an independent third-party valuation of our common stock to be distributed in the Distribution.

Furthermore, the obligations of TOP to consummate the Merger are subject to the satisfaction or waiver (to the extent permitted by applicable law) of the following conditions:

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certain fundamental representations and warranties of AquaMed and Merger Sub being true and correct in all respects in each case as of the date of the Merger Agreement and as of the closing date of the Merger as if made as of the closing date of the Merger;

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the covenants and agreements being performed by AquaMed and Merger Sub in all material respects at or prior to the effective time of the Merger;

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the absence of any AquaMed Material Adverse Effect since the date of the Merger Agreement;

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AquaMed shall have completed an audit of its financial statements for the years ended December 31, 2017 and December 31, 2016 by an independent registered auditor; and

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we shall have delivered to TOP (a) resignation letters of any of our officers and directors, to be effective as of the Effective Time, who will not be continuing officers or directors of us, and (b) certified resolutions of our Board of Directors (i) causing our whole Board of Directors to consist of five directors as of the Effective Time, (ii) appointing to the Board of Directors such individuals as necessary to cause the Board of Directors as of the Effective Time to conform with the requirements set forth on Schedule 1.4 to the Merger Agreement, and (iii) appointing as officers of Parent such individuals as necessary to cause our officers as of the Effective Time to conform with the requirements set forth on Schedule 1.4 to the Merger Agreement. We shall also deliver resolutions, in our capacity as the sole member of the surviving company as of the Effective Time, appointing persons to the Board of Managers of the surviving company, and resolutions of such Board of Managers appointing persons to serve as officers of the surviving company.

To the extent permitted by applicable law, each party to the Merger Agreement may waive, at its sole discretion, any of the conditions to its respective obligations to complete the Merger.

Regulatory Approvals

We must complete the necessary registration under U.S. federal securities laws of the AquaMed common stock to be issued in the Distribution and the Merger. We must also complete the applicable listing requirements of the Nasdaq Capital Market for such shares.

Other than these requirements, we do not believe that any other material governmental or regulatory filings or approvals will be necessary to consummate the Spin-Off or the Merger.

Accounting Treatment

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THE MERGER AGREEMENT

The following is a summary of material provisions of the Merger Agreement, which we entered into on November 27, 2018. This summary is qualified in its entirety by reference to the full text of the Merger Agreement which is filed as an exhibit to our Registration Statement on Form S-1 of which this prospectus forms a part.

The Merger

Under the Merger Agreement and in accordance with Delaware law, Merger Sub will merge with and into TOP, with TOP continuing as the surviving company. As a result of the Merger, TOP will become a wholly-owned subsidiary of AquaMed. As a result of the Merger, immediately after the Effective Time and consummation of the Private Placement, before giving effect to any fees payable in equity to financial advisors or other intermediaries, the current members of TOP and the third-party investors that participate in the Private Placement are expected to hold approximately 90% of the total number of shares of AquaMed common stock outstanding (on a fully diluted basis).

Closing and Effective Time

The Merger will occur following the consummation by Alliqua of the Internal Reorganization and Spin-Off pursuant to the Asset Contribution and Separation Agreement between Alliqua and AquaMed and all other Separation Agreements (as defined below) and the consummation of the Adynxx Merger.

Under the terms of the Merger Agreement, the closing of the Merger will take place on a date and at a time to be specified by the parties to the Merger Agreement (the “Closing Date”), which will be no later than the third business day after the satisfaction or, to the extent permitted by applicable law, waiver of the conditions set forth in the Merger Agreement and discussed below in “Conditions to Consummation of the Merger”.

On the Closing Date, Merger Sub and TOP will execute and file with the office of the Secretary of State of the State of Delaware the necessary certificate of merger executed in accordance with the Delaware Limited Liability Company Act. The Merger will become effective at the time of filing of the necessary certificate of merger, or at such later time as is agreed upon by the parties and set forth in such certificate of merger.

Merger Consideration

At the effective time of the Merger, all of the outstanding membership units of TOP will be automatically converted into the right to receive, in the aggregate, merger consideration consisting of shares of AquaMed common stock. Immediately after the effective time of the Merger and consummation of the Private Placement, before giving effect to any fees payable in equity to financial advisors or other intermediaries, the current members of TOP and the third-party investors that participate in the Private Placement are expected to hold approximately 90% of the total number of shares of AquaMed common stock outstanding (on a fully diluted basis) (the “Merger Consideration”), assuming that not more than $10 million is raised in the Private Placement.

Following the effective time of the Merger, all membership units of TOP will be automatically cancelled and cease to exist.

Transaction Agreements

The form of the Asset Contribution and Separation Agreement that will govern the terms of the Spin-Off is attached as an exhibit to the Merger Agreement. We will also enter into a Tax Matters Agreement and an Assumption Agreement (collectively and together with the Asset Contribution and Separation Agreement, the “Separation Agreements”) in connection with the Spin-Off. See “The Asset Contribution and Separation Agreement and Ancillary Agreements.”

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Conditions to Consummation of the Merger

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the Spin-Off having occurred pursuant to the Asset Contribution and Separation Agreement;

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the absence of any order issued by any governmental authority of competent jurisdiction or other legal impediment preventing or making illegal the consummation of the Merger; and

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we shall have received binding commitments from investors to consummate the Private Placement immediately prior to the effective time of the Merger.

In addition, our, and Merger Sub’s obligations to consummate the Merger are subject to the satisfaction or waiver (to the extent permitted by applicable law) of the following conditions:

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the covenants and agreements being performed by TOP in all material respects at or prior to the effective time of the Merger;

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TOP shall have obtained the consent of its sole member, and such consent shall not have been invalidated or revoked and shall remain in full force and effect;

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the absence of a TOP Material Adverse Effect since the date of the Merger Agreement;

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TOP shall have completed an audit of its financial statements for the years ended December 31, 2017 and December 31, 2016 by an independent registered auditor; and

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we shall have received an independent third-party valuation of our common stock to be distributed in the Distribution.

Furthermore, the obligations of TOP to consummate the Merger are subject to the satisfaction or waiver (to the extent permitted by applicable law) of the following conditions:

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the covenants and agreements being performed by AquaMed and Merger Sub in all material respects at or prior to the effective time of the Merger;

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the absence of any AquaMed Material Adverse Effect since the date of the Merger Agreement;

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AquaMed shall have completed an audit of its financial statements for the years ended December 31, 2017 and December 31, 2016 by an independent registered auditor; and

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To the extent permitted by applicable law, each party to the Merger Agreement may waive, at its sole discretion, any of the conditions to its respective obligations to complete the Merger.

Representations and Warranties

The Merger Agreement contains substantially reciprocal customary representations and warranties that AquaMed, Merger Sub and TOP made to each other as of specific dates.

The representations and warranties by each of AquaMed, Merger Sub and TOP in the Merger Agreement relate to, among other things:

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due organization, good standing, corporate power;

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capitalization;

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authority to enter into the Merger Agreement (and other transaction-related agreements);

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no conflicts with or violations of governance documents, other obligations or laws;

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financial statements;

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absence of undisclosed liabilities;

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absence of certain changes or events;

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litigation and similar actions;

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employee benefit matters;

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compliance with applicable laws and ownership of certain licenses;

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environmental matters;

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tax matters;

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IP matters;

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ownership of real and personal property;

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existence and enforceability of material contracts;

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labor and employment matters;

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insurance; and

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payment of fees to brokers or finders in connection with the Merger Agreement.

In addition, TOP made representations and warranties that relate to controlled substances.

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Many of the representations and warranties contained in the Merger Agreement are subject to a “material” or “material adverse effect” standard and none survive the closing.

Under the Merger Agreement, an “AquaMed Material Adverse Effect” means any effect, change, claim, event or circumstance (collectively “Effect”) that, considered together with all other Effects, is or would reasonably be expected to be or to become materially adverse to, or has or would reasonably be expected to have or result in a material adverse effect on: (1) the business, financial condition or results of operations of AquaMed and its subsidiaries taken as a whole, or (2) the ability of AquaMed to consummate the Merger or the other transactions contemplated by the Merger Agreement. However, any adverse effect, change, claim, event or circumstance, individually or in the aggregate, arising from or relating to the following will not be deemed either to constitute, or be taken into account in determining whether there has occurred an AquaMed Material Adverse Effect:

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conditions generally affecting the industries in which we participate or the U.S. or global economy as a whole, to the extent that such conditions do not have a disproportionate impact on us, taken as a whole, as compared to other industry participants;

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general conditions in the financial markets, and any changes therein (including any changes arising out of acts of terrorism, war, weather conditions or other force majeure events), to the extent that such conditions do not have a disproportionate impact on us, taken as a whole, as compared to other industry participants;

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changes in trading price or trading volume of our common stock; or

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changes in GAAP (or any interpretations of GAAP) applicable to us or any of our subsidiaries.

In addition, the term “TOP Material Adverse Effect” means any Effect that, considered together with all other Effects, is or would reasonably be expected to be or to become materially adverse to, or has or would reasonably be expected to have or result in a material adverse effect on: (1) the business, financial condition or results of operations of TOP taken as a whole, or (2) the ability of TOP to consummate the Merger or any of the other transactions contemplated by the Merger Agreement However, any adverse effect, change, claim, event or circumstance, individually or in the aggregate, arising from or relating to the following will not be deemed either to constitute, or be taken into account in determining whether there has occurred a TOP Material Adverse Effect:

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conditions generally affecting the industries in which TOP participates or the U.S. or global economy as a whole, to the extent that such conditions do not have a disproportionate impact on TOP, taken as a whole, as compared to other industry participants;

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general conditions in the financial markets, and any changes therein (including any changes arising out of acts of terrorism, war, weather conditions or other force majeure events), to the extent that such conditions do not have a disproportionate impact on TOP, taken as a whole, as compared to other industry participants;

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changes in GAAP (or any interpretations of GAAP) applicable to TOP or any of its subsidiaries; or

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the taking of any action expressly required to be taken pursuant to the Merger Agreement or requested by AquaMed to be taken pursuant to the terms of the Merger Agreement to the extent taken in accordance with such request.

Covenants

In the Merger Agreement, we have made certain covenants relating to our conduct in respect of our business, and TOP has made certain covenants relating to its conduct of its business, with certain exceptions specified in the Merger Agreement. Some of these covenants are not easily summarized. You are urged to read carefully the sections of the Merger Agreement entitled “Operation of the Business of the Parent Entities.” The following summarizes the more significant of these covenants:

Conduct of Business

Each of AquaMed, with respect to its business, and TOP, with respect to its existing business, agrees to carry on its respective business in the ordinary course consistent with past practice, pay its respective taxes

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and debts when due (subject to good faith disputes), pay or perform its respective other obligations when due, and to use reasonable best efforts to preserve intact its respective current business organization, keep available the services of current officers and key employees and preserve relationships with material customers, suppliers, licensors and governmental bodies.

Required Consent

Without the prior written consent of the other party, subject to certain exceptions and items disclosed in the schedules to the Merger Agreement, and solely with respect to AquaMed, in connection with the Private Placement, the Adynxx Merger, the transactions contemplated by the Asset Contribution and Separation Agreement, or the Distribution as contemplated by the Separation Agreements, none of AquaMed or TOP may take any or all of the following actions or authorize, commit or agree to take any of the following actions:

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declare, accrue, set aside or pay any dividend or make any other distribution in respect of any securities, or repurchase, redeem or otherwise reacquire the company’s units or other securities (except for (A) AquaMed’s right to repurchase shares of its restricted stock held by an employee of AquaMed upon termination of such employee’s employment; or (B) in connection with the withholding of shares of AquaMed common stock to satisfy tax obligations with respect to the exercise, vesting or settlement of equity awards);

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sell, issue, grant or authorize the sale, issuance or grant of: (A) any units of the company or other security; (B) any option, call, warrant or right to acquire any units of the company or other security (or whose value is directly related to units of the company); or (C) any instrument convertible into or exchangeable for any units of the company or other security (except for TOP’s right to raise up to $500,000);

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amend, waive any of its rights under any employment agreement or arrangement applicable to the employees of the company;

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amend or permit the adoption of any amendment to its certificate of formation, limited liability company agreement or other charter or organizational documents;

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(A) acquire any equity interest or other interest in any other entity; (B) form any subsidiary; or (C) effect or become a party to any merger, consolidation, share exchange, business combination, amalgamation, recapitalization, reclassification of limited liability company interests, unit split, reverse unit split, division or subdivision of units, consolidation of units or similar transaction;

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make any capital expenditure in excess of $75,000 (except that the applicable company may make any capital expenditure that is provided for in such company’s capital expense budget delivered or made available to the other party prior to the date of the Merger Agreement);

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other than in the ordinary course of business and consistent with past practices: (A) enter into or become bound by, or permit any of the assets owned or used by it to become bound by, any material contract; or (B) amend, terminate, or waive any material right or remedy under, any material contract;

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acquire, lease or license any right or other asset from any other person or sell or otherwise dispose of, or lease or license, any right or other asset to any other person (except in each case for assets: (A) acquired, leased, licensed or disposed of by the company in the ordinary course of business and consistent with past practices; or (B) that are immaterial to the business of the company, taken as a whole;

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make any pledge of any of its material assets or permit any of its material assets to become subject to any encumbrances, except for certain permitted encumbrances;

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lend money to any person;

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except as may be required by law with respect to TOP, establish, adopt, enter into or amend any employee plan or employment agreement (except as contemplated by the Merger Agreement), pay any bonus or make any profit-sharing or similar payment to, or increase the amount of the wages,

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salary, commissions, fringe benefits or other compensation (including equity-based compensation, whether payable in stock, cash or other property) or remuneration payable to, or adopt or agree to any retention arrangements with or for the benefit of, any of its managers or any of its officers or other employees (except for routine, reasonable salary increases to non-officer employees in the ordinary course of business and in accordance with past practices in connection with the customary employee review process);

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hire any employee at the level of Vice President or above or with an annual base salary in excess of $50,000, or promote any employee to the level of Vice President or above;

•

other than in the ordinary course of business and consistent with past practices or as required by concurrent changes in GAAP, change any of its methods of accounting or accounting practices in any respect;

•

make any material tax election;

•

commence any legal proceeding, except with respect to: (A) routine matters in the ordinary course of business and consistent with past practices; (B) in such cases where reasonably determined in good faith that the failure to commence suit would result in a material impairment of a valuable aspect of its business (provided that such party consults with the other party and considers the views and comments of the other party with respect to such legal proceedings prior to commencement thereof); or (C) in connection with a breach of the Merger Agreement or the transactions contemplated by the Merger Agreement;

•

settle any legal proceeding or other material claim, other than pursuant to a settlement: (A) that results solely in monetary obligation involving payment by of the amount specifically reserved in accordance with GAAP with respect to such legal proceedings or claim on such company’s latest balance sheet; or (B) that results solely in monetary obligation involving only the payment of monies of not more than $20,000 in the aggregate; or

•

agree or commit to take any of the foregoing actions.

In addition, AquaMed agreed not to accelerate collection of any accounts receivable without the prior written consent of TOP.

Private Placement

We and TOP agreed to use reasonable best efforts to arrange and to consummate the Private Placement on terms and conditions reasonably acceptable to us and TOP. In addition, we and TOP have agreed to use reasonable best efforts, as applicable, to cooperate in all aspects necessary or reasonably requested by us or TOP in connection with the arrangement and consummation of the Private Placement, including, without limitation, (A) participating in a reasonable number of meetings, presentations, and meetings with, and presentations to, prospective investors; (B) assisting with the marketing and due diligence efforts with respect to the Private Placement; (C) furnishing financial and other information regarding us, TOP and our respective subsidiaries, as required by the Private Placement; and (D) to obtain waivers, consents, estoppels and approvals from other parties to material leases, encumbrances and contracts to which we or TOP are a party, in each case to the extent required by the terms of the Private Placement. We also agreed to consult in good faith with TOP and its professional advisers regarding the material aspects of the Private Placement, including the form and manner thereof and to consider in good faith comments provided by TOP and its professional advisers in consummating the Private Placement. We and TOP are obligated to update any required information in order to ensure that such information does not contain any untrue statement of material fact or omit to state any material fact necessary in order to make the statements contained therein not materially misleading, as and to the extent required by the terms of the Private Placement.

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Other Covenants and Agreements

The Merger Agreement contains certain other covenants and agreements, including covenants (with certain exceptions specified in the Merger Agreement) relating to:

•

delivery of audited financial statements of each of AquaMed and TOP for the fiscal year ended December 31, 2018 on or before March 1, 2019;

•

cooperation among the parties relating to the prompt preparation and filing of the registration statement of which this prospectus forms a part in connection with the Distribution;

•

cooperation among the parties to obtain all governmental approvals and consents necessary to consummate the Merger and the other transactions;

•

resignations of the officers and directors of AquaMed and TOP;

•

public disclosure of the Merger and the other transactions contemplated by the Merger Agreement;

•

implementation of internal controls over financial reporting;

•

delivery of audited financial statements of each of AquaMed and TOP;

•

transaction expenses; and

•

obtaining the necessary member and stockholder approvals of each of AquaMed, Merger Sub and TOP.

Amendment; Extension; Waiver

The Merger Agreement may be amended by the parties at any time. Prior to the effective time of the Merger, the parties may extend the time for the performance of any of the obligations or other acts of the parties or waive any inaccuracies in the representations and warranties or compliance with any of the agreements or conditions contained in the Merger Agreement.

Termination of the Merger Agreement

The Merger Agreement may be terminated at any time before the effective time of the Merger by the mutual written consent of us and TOP. It may also be terminated by either us or TOP if:

•

The Merger Agreement may also be terminated by:

•

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THE ASSET CONTRIBUTION AND SEPARATION AGREEMENT AND
ANCILLARY AGREEMENTS

The following are summaries of the material provisions of the Asset Contribution and Separation Agreement and ancillary agreements that we intend to enter into before the Distribution. These summaries are qualified in their entirety by reference to the full text of the Asset Contribution and Separation Agreement and ancillary agreements which are filed as exhibits to our Registration Statement on Form S-1, as amended, of which this prospectus forms a part.

Asset Contribution and Separation Agreement

We intend to enter into an Asset Contribution and Separation Agreement with Alliqua before the Distribution. The Asset Contribution and Separation Agreement will set forth our agreements with Alliqua regarding the principal actions to be taken in connection with the Spin-Off. It will also set forth other agreements that govern aspects of our relationship with Alliqua following the Spin-Off.

Internal Reorganization. The Asset Contribution and Separation Agreement will provide for the transfers of assets and assumptions of liabilities that are necessary in advance of the Distribution so that we hold the assets of, and the liabilities associated with, Alliqua’s custom hydrogels business, and certain additional actions related to the Spin-Off that will occur prior to the Distribution.

Merger Agreement. The Asset Contribution and Separation Agreement requires us to use reasonable best efforts to consummate the Merger and the other transactions contemplated by the Merger Agreement.

Representations and Warranties. In general, Alliqua will make representations or warranties that the material items of equipment and other tangible assets owned by or leased to, and necessary for the operation of, our business that are part of the assets to be contributed by Alliqua to AquaMed are adequate for the uses to which they are being put by Alliqua, are in good and safe working condition and repair (ordinary wear and tear excepted) and are adequate for the conduct of AquaMed business in the manner in which such business is currently being conducted. In addition, Alliqua will represent that all of said tangible assets are being delivered to AquaMed free and clear of any encumbrances, except for certain permitted encumbrances.

Consents; Assignments Not Effected at Closing. The parties will use commercially reasonable efforts to obtain any consent required for the transfer and assignment of all contributed contracts, to AquaMed, and to obtain any release, substitution or amendment required to novate any and all contributed contracts or to obtain in writing the unconditional release from such Alliqua Contributed Contracts, and to permit AquaMed to assume the rights and liabilities under such contracts. If any consent required for Alliqua to transfer or assign any of the contributed contracts to AquaMed is not obtained on or before closing, for a two-year period from and after the closing date, Alliqua and AquaMed will use commercially reasonable efforts, and shall cooperate with each other, following the closing, at the sole cost and expense of AquaMed, to obtain such consent. AquaMed has agreed to reimburse Alliqua for any costs or expenses incurred in connection with continued possession or ownership of such contract.

The Distribution. The Asset Contribution and Separation Agreement will govern Alliqua’s and our respective rights and obligations regarding the proposed Distribution. Prior to the Distribution, Alliqua will deliver all the issued and outstanding shares of our common stock to the Distribution Agent. Following the Distribution, the Distribution Agent will electronically deliver the shares of our common stock to Alliqua stockholders based on the distribution ratio.

Conditions. The Asset Contribution and Separation Agreement will also provide that several conditions must be satisfied or waived by Alliqua in its sole and absolute discretion before the Distribution can occur. For further information about these conditions, see “The Transactions — Conditions to the Spin-Off.” The board of directors of Alliqua may, in its sole and absolute discretion, determine the Record Date and the Distribution Date.

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Non-solicitation. The Asset Contribution and Separation Agreement will also provide that Alliqua and we will be restricted from, whether for its own account or for the account of any person, soliciting, endeavoring to entice away from, or otherwise interfering with the relationship with, any person that, during the restricted period, is employed by or otherwise engaged to perform services for the other party (including such party’s subsidiaries and other entities the financial statements of which are consolidated with those of the party under GAAP).

Employee Matters. We expect certain AquaMed employees will continue with us after the closing. As of the closing, the salary, wages, bonus and/or incentive compensation, and other employee benefit plans, programs, and arrangements with respect to such continuing employees shall be the sole responsibility of AquaMed, on such terms, if any, that AquaMed may determine to provide to such continuing employees. On and after the closing date, Alliqua will be responsible and will agree to assume or retain, pay, perform, fulfill and discharge, in due course in full (i) all liabilities under all of Alliqua’s benefit plans, (ii) all liabilities with respect to the employment, service, termination of employment or termination of service of all of the employees and former employees to the extent arising in connection with or as a result of employment with or the performance of services for Alliqua before, on or after the closing date, and (iii) all liabilities with respect to the employment, service, termination of employment or termination of service of all Alliqua group employees and former employees to the extent arising in connection with or as a result of employment with or the performance of services for AquaMed before the closing date, and liabilities arising in connection with any claims by any service provider to Alliqua for severance or other rights on account of a change in control in connection with the transactions contemplated by the Asset Contribution and Separation Agreement.

Indemnification. We and Alliqua will each agree to indemnify the other and certain affiliates and related persons against certain liabilities incurred in connection with the Spin-Off and our and Alliqua’s respective businesses. These indemnities are principally designed to place financial responsibility for the obligations and liabilities of our business with us and financial responsibility for the obligations and liabilities of Alliqua’s business with Alliqua. Specifically, each party will indemnify, defend and hold harmless the other party, its affiliates and subsidiaries and each of its officers, directors, employees and agents for any loss, damage, liability, judgment, award, fee or expense (including reasonable expenses of investigation and reasonable attorneys’, experts’, accounting, or advisory fees and expenses in connection with any action, suit or proceeding whether involving a third-party claim or a claim solely between the parties hereto), including any incidental, indirect or consequential damages, losses, liabilities or expenses, but excluding any lost profits or diminution in value (collectively, “Damages”) arising out of or due to the breach of any covenant or obligation or representation of such party contained in the Asset Contribution and Separation Agreement.

In addition, Alliqua will indemnify us for Damages that are incurred or suffered based upon, arising out of, with respect to, or by reason of:

•

any liabilities retained by Alliqua.

Furthermore, we will indemnify Alliqua for Damages that are incurred or suffered based upon, arising out of, with respect to, or by reason of:

•

contracts contributed to us by Alliqua, whether rising prior to, on, or after the closing date;

•

ownership, use or operation after the closing date of the assets contributed to us by Alliqua;

•

conducting our business after the closing date; or

•

any liabilities assumed by us.

The amount of each party’s indemnification obligations will be subject to reduction by any insurance proceeds received by the party being indemnified.

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Tax Matters Agreement

The Tax Matters Agreement generally sets out the respective rights, responsibilities, and obligations of Alliqua and AquaMed with respect to taxes (including taxes arising in the ordinary course of business and taxes incurred as a result of the Spin-Off), tax attributes, tax returns, tax contests and certain other related tax matters. A copy of the Tax Matters Agreement is included as an exhibit to our Registration Statement on Form S-1, of which this prospectus forms a part, and is incorporated in this prospectus by reference.

The Tax Matters Agreement allocates responsibility for the preparation and filing of certain tax returns (and the payment of taxes reflected thereon), including Alliqua’s consolidated federal income tax return, tax returns associated with both the Alliqua business and the AquaMed business, and tax returns associated with either the Alliqua business or the AquaMed business, and provides for certain reimbursements by the parties.

Under the Tax Matters Agreement, Alliqua will generally be liable for its own taxes and taxes of all of its subsidiaries (other than AquaMed, the taxes for which AquaMed shall be liable) for all tax periods (or portion thereof) ending on the date of the separation. AquaMed will be responsible for its taxes, for taxes of Alliqua arising as a result of the Spin-Off and for any transfer taxes incurred in the Spin-Off and for taxes attributable to the AquaMed business.

Each of Alliqua and AquaMed will indemnify each other against any taxes allocated to such party under the Tax Matters Agreement or arising from any breach of its covenants thereunder, and related out-of-pocket costs and expenses.

Assumption Agreement

The Assumption Agreement generally sets out the respective rights, responsibilities, and obligations of Alliqua and AquaMed with respect to the assets and liabilities being transferred from Alliqua to AquaMed. Pursuant to the Assumption Agreement, Alliqua will assign to AquaMed all of Alliqua’s right, title and interest in the assets owned by Alliqua which primarily relate to our hydrogel business and AquaMed will assume all of the liabilities relating thereto or which primarily relate to our hydrogel business. A copy of the Assumption Agreement is included as an exhibit to our Registration Statement on Form S-1, of which this prospectus forms a part, and is incorporated in this prospectus by reference.

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MATERIAL U.S. FEDERAL INCOME TAX CONSEQUENCES OF THE DISTRIBUTION

General

The following is a summary description of the material U.S. federal income tax aspects of the Spin-Off. This summary is not intended as a complete description of all of the tax consequences of the Spin-Off and does not discuss tax consequences under the laws of state, local or foreign governments or any other jurisdiction. Moreover, the tax treatment of a stockholder may vary, depending upon his, her or its particular situation. In this regard, special rules not discussed in this summary may apply to some of our stockholders. In addition, this summary applies only to shares which are held as capital assets. The following discussion may not be applicable to a stockholder who acquired his, her or its shares by exercising stock options or otherwise as compensation.

The following discussion is based on currently existing provisions of the Code, existing, proposed and temporary treasury regulations promulgated under the Code and current administrative rulings and court decisions. All of the foregoing are subject to change, which may or may not be retroactive, and any of these changes could affect the validity of the following discussion.

Each stockholder is urged to consult his, her or its own tax advisor as to the particular tax consequences to him, her or it of the Spin-Off described herein, including the applicability and effect of any state, local or foreign tax laws, and the possible effects of changes in applicable tax laws.

Tax Consequences of the Spin-Off

For U.S. federal income tax purposes, the distribution by Alliqua of the shares of AquaMed common stock will not be eligible for treatment as a tax-free distribution. Accordingly, each holder of Alliqua common stock who receives shares of AquaMed common stock in the Spin-Off generally will be treated as if such stockholder received a taxable distribution in an amount equal to the fair market value of AquaMed common stock received (including any fractional share deemed to be received by and sold on behalf of the stockholder), which will result in: (a) a dividend to the extent of such stockholder’s ratable share of Alliqua’s current and accumulated earnings and profits; then (b) a reduction in such stockholder’s basis in Alliqua’s common stock (but not below zero) to the extent the amount received exceeds the amount referenced in clause (a); and then (c) gain from the sale or exchange of Alliqua common stock to the extent the amount received exceeds the sum of the amounts referenced in clauses (a) and (b). Each stockholder’s basis in his, her or its AquaMed common stock will be equal to the fair market value of such stock at the time of the Spin-Off. A stockholder’s holding period for such shares will begin the day after the Spin-Off date.

A corporate level U.S. federal income tax will be payable by the consolidated group of which Alliqua is the common parent if gain realized in the Spin-Off exceeds any net operating losses that may be available to offset such gain. The tax would be based upon the gain, if any, computed as the difference between the fair market value of the AquaMed common stock and Alliqua’s adjusted basis in such stock. Alliqua expects that it will have sufficient losses available to fully offset any gain realized as a result of the Spin-Off.

Alliqua’s earnings and profits generally will be increased by any gain Alliqua recognizes as a result of the contribution of assets to AquaMed and the subsequent Spin-Off. Alliqua will not be able to advise stockholders of the amount of its earnings and profits until after the end of the tax year in which the Spin-Off occurs.

In addition, Alliqua or other applicable withholding agents may be required or permitted to withhold at the applicable rate on all or a portion of the Spin-Off distribution (including cash paid in lieu of fractional shares) payable to non-U.S. stockholders, and any such withholding would be satisfied by Alliqua or the other applicable withholding agent either withholding and selling a portion of our shares of common stock otherwise distributable to non-U.S. stockholders, or withholding such amount from any cash distribution otherwise payable to such non-U.S. stockholders. Any shares or cash so withheld shall be treated as if they were paid to such non-U.S. stockholders. Although Alliqua will be ascribing a value to shares of AquaMed common stock it distributes for tax purposes, this valuation is not binding on the IRS or any other tax authority. These taxing authorities could ascribe a higher valuation to such shares,

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particularly if such shares trade at prices significantly above the value ascribed to them by Alliqua in the period following the distribution. Such a higher valuation may cause a larger reduction in the tax basis of a stockholder’s shares of Alliqua common stock or may cause a stockholder to recognize additional dividend or capital gain income.

Back-up Withholding Requirements

United States information reporting requirements and backup withholding may apply with respect to dividends paid on, and proceeds from the taxable sale, exchange or other disposition of, AquaMed common stock unless the stockholder: (a) is a corporation or non-U.S. holder or comes within certain other exempt categories, and, when required, demonstrates these facts (including by providing any applicable IRS form); or (b) provides a correct taxpayer identification number, certifies as to no loss of exemption from backup withholding and otherwise complies with applicable requirements of the backup withholding rules. A stockholder who does not supply us with his, her or its correct taxpayer identification number may be subject to penalties imposed by the IRS. Any amount withheld under these rules will be creditable against the stockholder’s U.S. federal income tax liability. Stockholders should consult their tax advisors as to their qualification for exemption from backup withholding and the procedure for obtaining such an exemption. If information reporting requirements apply to a stockholder, the amount of dividends paid with respect to the stockholder’s shares will be reported annually to the IRS and to the stockholder.

Stockholders should consult their own tax advisors as to the particular tax consequences of the Spin-Off to them.

USE OF PROCEEDS

We will not receive any proceeds from the distribution of our common stock in the Spin-Off.

DETERMINATION OF OFFERING PRICE

No consideration will be paid for the shares of our common stock in the Spin-Off.

DIVIDEND POLICY

We have never declared or paid any cash dividends on our common stock. For the foreseeable future, we anticipate that all available funds and any earnings generated in our business will be used to finance the growth of our business and will not be paid out as dividends to our shareholders. Any future determination related to our dividend policy will be made at the discretion of our Board of Directors and will depend upon, among other factors, our results of operations, financial condition, capital requirements, contractual restrictions, business prospects and other factors our Board of Directors may deem relevant.

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CAPITALIZATION

The following table sets forth our cash and capitalization as of September 30, 2018, on a historical basis and on pro forma basis to give effect to the Spin-Off and the Merger, as if they occurred on September 30, 2018. The historical combined balance sheet data presented in the capitalization table as of September 30, 2018 for AquaMed is derived from AquaMed’s unaudited condensed financial statements and for TOP is derived from TOP’s unaudited condensed consolidated interim financial statements, included elsewhere in this prospectus. The unaudited pro forma combined financial information was prepared using the purchase method of accounting, with TOP treated as the “acquirer” of AquaMed for accounting purposes. The effect of the Merger presented below includes the impact of preliminary purchase accounting adjustments. The pro forma information presented below is derived from the “Unaudited Pro Forma Combined Financial Statements” included elsewhere in this prospectus. In addition, you should review the following table in conjunction with “Management’s Discussion and Analysis of Financial Condition and Results of Operations of AquaMed,” “Management’s Discussion and Plan of Operations of TOP,” “Liquidity and Capital Resources Following The Transactions” and the financial statements and accompanying notes included elsewhere in this prospectus.

(in thousands)	TO Pharmaceuticals as of September 30, 2018			AquaMed Technologies, Inc. as of September 30, 2018		Effect of Mergers		Pro Forma Combined
Cash		$	—		—		—		$	—
Short-term obligations:
Current maturities of long-term debt		$	—							—
Current maturities of capitalized lease obligations			—							—
Total short-term debt and current obligations of long-term debt			—		—		—			—
Long-term obligations:
Total long-term debt		$	—							—
Less: current maturities of long-term debt			—							—
Total long-term debt, net of current maturities			—		—		—			—
Stockholders’ equity:
Member’s Deficit		$	(2,435)		—		2,435			—
Parent’s Net Investment			—		539		(539)			—
Preferred stock										—
Common stock							1			1
Additional paid in capital							(1,897)			(1,897)
Accumulated deficit										—
Accumulated other comprehensive (loss) income										—
Total equity			(2,435)		539		—			(1,896)
Total capitalization		$	(2,435)		539		—		$	(1,896)

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SELECTED HISTORICAL FINANCIAL DATA FOR AQUAMED

The following tables present our selected historical financial data for the periods and as of the dates indicated.

Our historical results are not necessarily indicative of future operating results, and the results for any interim period are not necessarily indicative of the results that may be expected for a full fiscal year.

You should read this information in conjunction with the section titled “Management’s Discussion and Analysis of Financial Condition and Results of Operations of AquaMed” and our financial statements and the related notes thereto included elsewhere in this prospectus.

Statements of Operations Data:

(in thousands)	Nine Months Ended September 30, (unaudited)						Year Ended December 31,
(in thousands)	2018			2017			2017			2016
REVENUES:
Revenue, net of returns, allowances and discounts		$	1,752		$	1,330		$	1,992		$	2,152
Cost of revenues			(1,354)			(1,326)			(1,845)			(2,266)
Gross profit (loss)			398			4			147			(114)
OPERATING EXPENSES:
Selling, general and administrative			(1,733)			(775)			(1,116)			(1,750)
Total operating expenses			(1,733)			(775)			(1,116)			(1,750)
Loss from operations			(1,335)			(771)			(969)			(1,864)
OTHER INCOME:
Sundry			12			—			—			25
Total other income			12			—			—			25
LOSS FROM OPERATIONS BEFORE TAX			(1,323)			(771)			(969)			(1,839)
INCOME TAX BENEFIT			—			12			16			63
NET LOSS		$	(1,323)		$	(759)		$	(953)		$	(1,776)

Balance Sheet Data:

(in thousands)	September 30, 2018			December 31, 2017
	(unaudited)
Consolidated Balance Sheet Data:
Accounts receivable, net		$	172		$	99
Inventory, net			183			93
Prepaid expenses and other current assets			341			7
Total assets			1,153			894
Total liabilities			614			269
Total Parent Net Investment			539			625
Total liabilities and Parent net investment		$	1,153		$	894

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SELECTED HISTORICAL CONSOLIDATED FINANCIAL DATA FOR TOP

The following tables present TOP’s selected historical consolidated financial and for the periods and as of the dates indicated.

TOP’s historical results are not necessarily indicative of future operating results, and the results for any interim period are not necessarily indicative of the results that may be expected for a full fiscal year.

You should read this information in conjunction with the section titled “Management’s Discussion and Analysis of Financial Condition and Plan of Operations of TOP” and TOP’s consolidated financial statements and notes thereto, in each case, included elsewhere in this prospectus.

Consolidated Statements of Operations Data:

	Nine Months Ended September 30, (unaudited)						Year Ended December 31,
	2018			2017			2017			2016
OPERATING EXPENSES:
Selling, general and administrative		$	296,779		$	450,936		$	502,574		$	954,216
Research and development			340,109			73,822			235,096			106,179
Total operating expenses			636,888			524,758			737,670			1,060,395
Loss from operations			(636,888)			(524,758)			(737,670)			(1,060,395)
NET LOSS		$	(637)		$	(525)		$	(738)		$	(1,060)

Balance Sheet Data:

	September 30, 2018			December 31, 2017
	(unaudited)
Consolidated Balance Sheet Data:
Licenses, net of accumulated amortization			435,563			454,500
Total assets			529,063			471,500
Total liabilities			2,963,916			2,269,465
Members’ deficit		$	(2,434,853)		$	(1,797,965)

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UNAUDITED PRO FORMA CONDENSED COMBINED FINANCIAL INFORMATION

The following TOP and AquaMed unaudited pro forma condensed combined financial statements, which are referred to in this prospectus as the unaudited pro forma financial information, gives effect to the proposed merger in which TOP will become a 100% owned subsidiary of AquaMed. The Unaudited Pro Forma Condensed Combined Balance Sheet is presented as if the Merger had closed on September 30, 2018. The Unaudited Pro Forma Condensed Combined Statement of Operations are presented as if the Merger had closed on January 1, 2017.

The unaudited pro forma combined financial information included herein is derived from the historical financial statements of AquaMed and TOP, included elsewhere herein. The preparation of the unaudited pro forma financial information and related adjustments required management to make certain assumptions and estimates, which it believes to be reasonable, which are described in the section entitled “Notes to Unaudited Pro Forma Combined Financial Information.” Management has not performed a complete and thorough valuation analysis necessary to determine the fair market values of all of the AquaMed assets to be acquired and liabilities to be assumed, and accordingly, as described in Note 2(a) below, the unaudited pro forma combined financial information includes a preliminary allocation of the purchase price to reflect the fair value of those assets and liabilities. A final determination of fair values of AquaMed assets and liabilities, along with the fair value of the common shares to be issued, cannot be made prior to the completion of the Merger, will be based on the actual net assets of AquaMed that exist as of the date of completion of the Merger along with the fair value of the common shares to be issued. Consequently, amounts preliminarily assumed for acquisition consideration and allocated to acquired assets and assumed liabilities could change significantly from those amounts used in the unaudited pro forma condensed combined financial statements presented below.

The unaudited financial information are provided for informational purposes only and does not purport to represent what the combined results of operations actually would have been if the Merger had occurred on January 1, 2017 or what those results will be for any future periods or what the combined balance sheet would have been if the Merger had occurred on September 30, 2018 or what the combined balance sheet will be on any future date. The pro forma adjustments are based on information current as of the time of this filing or as otherwise indicated; and has not been adjusted to reflect any matters not directly attributable to implementing the merger. No adjustment, therefore, has been made for actions which may be taken once the Merger is complete, such as any of TOP integration plans related to AquaMed. In connection with the plan to integrate the operations of TOP and AquaMed following the completion of the merger, TOP anticipates that nonrecurring charges, such as costs associated with systems implementation and other costs related to exit or disposal activities, could be incurred. TOP is not able to determine the timing, nature and amount of these charges as of the date of this prospectus. However, these charges could affect the results of operations of TOP and AquaMed, as well as those of the combined company following the completion of the Merger, in the period in which they are recorded. The unaudited pro forma condensed combined financial statements do not include the effects of the costs associated with any restructuring or integration activities resulting from the merger, as they are nonrecurring in nature and were not factually supportable at the time that the unaudited pro forma condensed combined financial statements were prepared. Additionally, the unaudited pro forma adjustments do not give effect to any nonrecurring or unusual restructuring charges that may be incurred as a result of the integration of the two companies or any anticipated disposition of assets that may result from such integration. As a result, the actual amounts recorded in the future combined financial statements of TOP will differ from the amounts reflected in the unaudited pro forma combined financial information, and the differences may be material.

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UNAUDITED PRO FORMA CONDENSED COMBINED BALANCE SHEET
As of September 30, 2018

(in thousands)	TO Pharmaceuticals(1)			AquaMed Technologies, Inc.(1)			Transaction Adjustments			Footnote Reference	Pro Forma Combined
ASSETS:
Current Assets:
Cash and cash equivalents		$	—		$	—		$	—			$	—
Accounts receivable			—			172			—				172
Inventory, net			—			183			—				183
Prepaid expenses and other current assets			94			341			—				435
Total current assets			94			696			—				790
Improvements and equipment, net			—			279			—				279
Intangible assets, net			436			—			—				436
Goodwill			—			—			—				—
Other assets			—			178			—				178
Total assets		$	530		$	1,153		$	—			$	1,683
LIABILITIES AND STOCKHOLDERS’ EQUITY
Current Liabilities:
Accounts payable		$	89		$	305		$	—			$	394
Accrued expenses and other current liabilities			316			256			—				572
Due to parent			2,560			—			—				2,560
Total current liabilities			2,965			561			—				3,526
Long-term debt									—				—
Other long-term liabilities			—			53			—				53
Total liabilities			2,965			614			—				3,579
Commitments and Contingencies
Stockholders’ Equity
Member Deficit			(2,435)						2,435	3(b)			—
Parent’s Net Investment			—			539			(539)	2(a), 3(a)			—
Preferred Stock			—			—			—				—
Common Stock			—			—			1	3(a), 3(b)			1
Additional paid-in capital			—			—			(1,897)	3(a), 3(b)			(1,897)
Accumulated deficit			—			—			—	2(a), 3(a), 3(b)			—
Total stockholders’ equity			(2,435)			539			—				(1,896)
Total liabilities and stockholders’ equity		$	530		$	1,153		$	—			$	1,683

See Notes to Unaudited Pro Forma Combined Financial Information.

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Notes to Unaudited Pro Forma Combined Financial Information

BASIS OF PRESENTATION

The unaudited pro forma combined financial information has been derived from financial statements prepared in accordance with the Generally Accepted Accounting Principles (“GAAP”) and reflects the proposed Merger of AquaMed with TOP.

The underlying financial information of TOP has been derived from the audited consolidated financial statements of TOP for the year ended December 31, 2017 and the unaudited condensed consolidated financial statements as of and for the nine months ended September 30, 2018, included elsewhere herein. The underlying financial information of AquaMed has been derived from the audited financial statements of AquaMed for the year ended December 31, 2017 and the unaudited condensed financial statements as of and for the nine months ended September 30, 2018, included elsewhere herein.

The Merger has been treated as an acquisition of a business, with TOP as the accounting acquirer and AquaMed as the acquiree, assuming that the Merger had been completed on January 1, 2017, for the unaudited pro forma combined statement of operations and on September 30, 2018, for the unaudited pro forma combined balance sheet.

This unaudited pro forma combined financial information is not intended to reflect the financial position and results of operations which would have actually resulted had the Merger been effected on the dates indicated. Further, the unaudited pro forma results of operations and balance sheet are not necessarily indicative of the results of operations that may be achieved in the future or what may be reflected in any future balance sheet. No account has been taken of the impact of transactions that have occurred or might occur subsequent to the dates referred to above. No adjustment, therefore, has been made for actions which may be taken once the merger is complete, such as any integration plans related to AquaMed.

The unaudited pro forma financial information reflects the preliminary assessment of fair values to the assets acquired and liabilities assumed, along with the consideration to be given. Fair value estimates were determined based on preliminary discussions between TOP and AquaMed management, and due diligence efforts. Management believes the carrying value of Aquamed’s assets and liabilities along with the consideration to be given is a close proxy for the preliminary fair value.

ALLOCATION

(a)

Preliminary Allocation of Merger Consideration to Assets Acquired

Receivables and other current assets		513
Property and equipment		279
Inventory		183
Goodwill		0
Other noncurrent assets		178
Other liabilities assumed		(614)
Preliminary valuation of common shares to be issued	$	539

The value prescribed to the shares AquaMed will receive is a preliminary valuation and will be revalued upon the closing of the PIPE transaction.

PRO FORMA TRANSACTION ADJUSTMENTS

The unaudited pro forma financial information reflects the following adjustments:

(a)

Recapitalization of AquaMed’s Parent’s Net Investment

An adjustment to recapitalize AquaMed’s Parent’s Net Investment of $0.539 million was reflected in the unaudited pro forma combined balance sheet as of September 30, 2018.

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BUSINESS OF AQUAMED

Our Company

Industry and Markets

Hydrogels are currently being marketed in the U.S. and abroad for the following applications:

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Drug Delivery. Delivering medication through hydrogel patches has important advantages over traditional methods of drug delivery. Hydrogel patches are less intrusive, painless, allow for pre-planned medication time periods, can potentially release medication in a manner consistent with the body’s own glandular activity (by avoiding dosage spikes and/or digestive alteration), and minimize side effects related to the medication via injection or ingestion.

•

Other Medical Applications. Hydrogel patches are being used for transdermal applications such as hormone replacement therapy and contraception, treatment of acne, shingles, diabetes, motion sickness, treatment of angina with nitroglycerin and treatment of smoking addiction using nicotine and palliatives (i.e., pain relievers).

•

Non-Prescription Therapeutic Applications. Hydrogel patches are also used in the medical community and are also directly marketed to consumers for topical application of over the counter (“OTC”) drugs such as non-prescription acne treatments, pain relievers, diet preparations, cough suppressants, treatment of warts, calluses and corns, and pain relief.

•

Moist Wound and Burn Dressings. Hydrogel dressings have long been used for treating wounds and burns. Clinical trials have demonstrated the benefits of moist wound healing versus traditional dressings. Some of these benefits include immediate anti-inflammatory effects, allowing for freer cell flow and less scarring, increased absorption of exudate, and accelerated healing.

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Components of Medical Devices. Several medical devices utilize hydrogels as components. These devices include active drug delivery systems such as iontophoresis, warming and cooling devices, and medical electrodes.

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Cosmetic Applications. Hydrogel patches and applications can deliver cosmetic skin care products to consumers and skin care providers for uses that include moisturizers, face masks, cooling masks and applicators.

Sales and Marketing

We continue to focus on sales and marketing efforts in the United States. As of September 30, 2018, we did not have any employees solely dedicated to sales, however, some of our employees perform in a sales capacity in addition to their other duties.

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Competition

To our knowledge, AquaMed is one of three manufacturers using electron beam technology for high performance hydrogels for the wound care, cosmetic and drug delivery industries.

Sources and Availability of Raw Materials; Principal Suppliers

In general, raw materials essential to our business are readily available from multiple sources. For reasons of quality assurance, availability, or cost effectiveness, certain components and raw materials are available only from a sole supplier. The principal suppliers for our raw materials are Berry Global, Inc., DeWolf Chemical, Inc. and Univar Inc. Our policy is to maintain sufficient inventory of components so that our production will not be significantly disrupted even if a particular component or material is not available for a period of time.

Because we have no direct control over these suppliers, interruptions or delays in the products and services provided by these parties may be difficult to remedy in a timely fashion. In addition, if such suppliers are unable or unwilling to deliver the necessary products or raw materials, we may be unable to redesign or adapt our technology to work without such raw materials or products or find alternative suppliers or manufacturers. In such events, we could experience interruptions, delays, increased costs or quality control problems, or be unable to sell the applicable products, all of which could have a significant adverse impact on our revenue.

Other than as discussed above, we believe that, due to the size and scale of production of our suppliers, there should be an adequate supply of raw materials from our other suppliers.

Customers

During the nine months ended September 30, 2018, one customer accounted for 62.5% of our contract manufacturing revenue. We are uncertain as to this customer’s intentions to use our services during the fiscal year ending December 31, 2019.

Patents, Proprietary Rights and Trademarks

We own or license trademarks covering our company and our products. We currently hold patent rights to one patent in Europe, which covers the use of lignin for inhibiting restenosis and thrombosis formation, and coated medical devices where the coating includes lignin. These patent rights are set to expire in September 2021. In addition, in connection with the Internal Reorganization, we expect to receive an exclusive license with right to sub-license from Specialty Pharmaceutical Products, L.L.C. (which is presently held by Alliqua) to two issued patents, one in the U.S. and one in Europe, which cover technology relating to a transdermal patch containing transcutol. The transdermal patch is effective to deliver lidocaine to a patient. These licensed patent rights are expected to expire in April 2032. We also rely upon trade secrets and continuing technological innovations to develop and maintain our competitive position.

Government Regulation

Product Regulation. Under the Federal Food, Drug and Cosmetic Act, medical devices are classified by the FDA into one of three classes — Class I, Class II or Class III — depending on the degree of risk associated with each medical device and the extent of control needed to ensure safety and effectiveness. While some applications of hydrogels fall under the jurisdiction of the FDA, hydrogels are generally classified as Class I exempt devices and the majority of the hydrogel products that we manufacture are thereby exempt from the FDA filing of any regulatory submissions and/or pre-market notification requirements. To the extent that any FDA regulatory submissions are required, we will be required to file these submissions and maintain all appropriate documentation. With respect to registering the manufacturing facility with the FDA under the Code of Federal Regulations, 21 CFR 820.1, Scope: Part A, it is stated that the regulation does not apply to manufacturers of component parts of finished devices. Currently, hydrogels are sold as component parts to various medical device/cosmetic manufacturers.

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Quality Assurance Requirements. The FDA enforces regulations to ensure that the methods used in, and the facilities and controls used for, the manufacture, processing, packing and holding of drugs and medical devices conform with current good manufacturing practice (CGMP). The CGMP regulations enforced by the FDA are comprehensive and cover all aspects of manufacturing operations, from receipt of raw materials to finished product distribution, insofar as they bear upon whether drugs meet all the identity, strength, quality and purity characteristics required of them. The CGMP regulations for devices, called the Quality System Regulation, are also comprehensive and cover all aspects of device manufacture, from pre-production design validation to installation and servicing, insofar as they bear upon the safe and effective use of the device and whether the device otherwise meets the requirements of the Federal Food, Drug and Cosmetic Act. To assure compliance requires a continuous commitment of time, money and effort in all operational areas.

The FDA also conducts periodic inspections of drug and device registered facilities to assess their current CGMP status. If the FDA were to find serious non-compliant manufacturing or processing practices during such an inspection, it could take regulatory actions that could adversely affect our business, results of operations, financial condition and cash flows. With respect to domestic establishments, the FDA could initiate product seizures or in some instances require product recalls and seek to enjoin a product’s manufacture and distribution. In certain circumstances, violations could support civil penalties and criminal prosecutions. In addition, if the FDA concludes that a company is not in compliance with CGMP requirements, sanctions may be imposed that include preventing that company from receiving the necessary licenses to export its products and classifying that company as an “unacceptable supplier”, thereby disqualifying that company from selling products to federal agencies.

We conduct audits of our outside manufacturers and believe that we and our suppliers and outside manufacturers are currently in compliance with CGMP requirements. We are currently registered as a device manufacturer and human tissue distributor with the FDA and we intend to register as a drug facility with the FDA when we are required to do so.

Environmental Regulation. We are subject to various laws and governmental regulations concerning environmental matters and employee safety and health in the U.S. and other countries. We have made, and continue to make, significant investments to comply with these laws and regulations. We cannot predict the future capital expenditures or operating costs required to comply with environmental laws and regulations. We believe that we are currently compliant with applicable environmental, health and safety requirements in all material respects. However, we cannot assure you that current or future regulatory, governmental, or private action will not have a material adverse effect on our performance, results or financial condition.

In the future, if a loss contingency related to environmental matters, employee safety, health or conditional asset retirement obligations is recognized, we would record a liability for the obligation and it may result in a material impact on net income for the annual or interim period during which the liability is recorded. The investigation and remediation of environmental obligations generally occur over an extended period of time, and therefore we do not know if these events would have a material adverse effect on our financial condition, liquidity, or cash flow, nor can we assure you that such liabilities would not have a material adverse effect on our performance, results or financial condition.

Federal and State Anti-kickback, Self-referral, False Claims and Similar Laws. Our relationships with physicians, hospitals and the marketers of our products are subject to scrutiny under various federal anti-kickback, self-referral, false claims and similar laws, often referred to collectively as healthcare fraud and abuse laws. Healthcare fraud and abuse laws are complex, and even minor, inadvertent violations can give rise to claims that the relevant law has been violated. Certain states have similar fraud and abuse laws, imposing substantial penalties for violations. Any government investigation or a finding of a violation of these laws would likely result in a material adverse effect on the market price of our common stock, as well as our business, financial condition and results of operations. We believe that we are currently compliant with applicable anti-kickback, self-referral, false claims in all material respects.

Research and Development Costs

For the years ended December 31, 2017 and 2016, we did not incur any research and development costs.

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We intend to commit capital resources to research and development only as our cash resources allow. We have incurred all costs associated with the launch of our proprietary products and will only require research and development expenses for product enhancements and modifications and to obtain additional reimbursement coverage, which we do not expect to be significant.

Employees

As of September 30, 2018, we had six full-time employees. Of these employees, two are involved with finance, sales, marketing, and administration and four are involved with manufacturing and regulatory matters. Our employees are not represented by a labor union or other collective bargaining groups, and we consider relations with our employees to be good. We currently plan to retain and utilize the services of outside consultants for additional research, testing, regulatory, legal compliance and other services on an as needed basis.

Properties

We maintain a combined corporate office and manufacturing facility in Langhorne, Pennsylvania, where we lease approximately 16,500 square feet of office and manufacturing space. Our lease expires on January 31, 2026. We believe that our facility is well maintained and are suitable and adequate for our current needs.

Legal Proceedings

From time to time, we may become involved in lawsuits, investigations and claims that arise in the ordinary course of business. As of the date of this prospectus, we are not a party to any litigation whereby the outcome of such litigation, if determined adversely to us, would materially affect our financial position, results of operations or cash flows.

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BUSINESS OF TOP

TOP was incorporated on October 21, 2015 in Delaware and is an early stage biopharmaceutical company engaged in the business of discovering, developing and commercializing drugs containing cannabinoids, which are based on a proprietary cannabinoid product platform, for the treatment of various diseases, disorders and medical conditions, discussed more fully below.

TOP owns an exclusive license covering certain intellectual property of Tikun Olam Ltd. (“TOL”), which is a principal owner of TOP, for worldwide pharmaceutical products. TOL, a privately held Israeli corporation, is a widely recognized leader in medical cannabis research and production. TOL was founded in 2005 by philanthropist Tsachi Cohen and received the first government-issued license to supply medical cannabis in the State of Israel. In building its business, TOP has capitalized and plans to continue to capitalize on the reputation and consistency of TOL’s strains. TOP also owns six provisional patent applications with the U.S. Patent Office and three patents pursuant to the Patent Cooperation Treaty. The provisional patent applications cover formulations that include cannabinoids and/or other substances for the purpose of treating various medical conditions and disorders.

TOP’s business is focused on research and development of potential pharmaceutical products based on compounds derived from TOL’s proprietary strains. Through collaboration with TOL and leading medical experts at major Israeli hospitals and research organizations, TOP has been able to initially focus its efforts on Crohn’s Disease, ulcerative colitis, agitation in Alzheimer’s or other dementia, autism spectrum disorder, Tourette syndrome and acute migraines.

TOP’s former subsidiaries have also exclusively sublicensed certain rights, in each case in connection the production, research, development, promotion, marketing, sale, distribution and commercialization of pharmaceutical products derived from the intellectual property of TOL and TOP to the extent of their rights in and outside the United States, to:

•

Tikkun Pharma, Inc., a Delaware corporation (“Tikkun Pharma”), TOP’s former ownership interest in which has recently been distributed pro rata to its members, as it relates to the prevention, management and treatment of autoimmune diseases, disorders or symptoms related thereto (other than certain diseases or otherwise as more particularly described in “Sublicenses”), and

•

Jay Pharma, Inc., a Canadian corporation (“Jay Pharma”), TOP’s former ownership interest in which has recently been distributed pro rata to its members, as it relates to the prevention, management and treatment of cancer and diseases, disorders or symptoms related thereto.

TOP’s Objectives and Business Strategy

TOP’s corporate strategy is to research and develop pharmaceutical medicine candidates containing cannabinoids based on TOL’s proprietary strains for use in the treatment of various diseases, disorders and medical conditions. Cannabinoids may be derived from the cannabis plant or synthesized. Cannabis is a category of plants that include three species and seven sub-species. Although over 160 compounds have been isolated from cannabis plants, most interest has centered on understanding the two major active components: Delta9-Tetrahydrocannibinol (“THC”), which appears to have psychoactive and other effects, and Cannabidiol (“CBD”), which appears to have anti-inflammatory and other effects.

Both plant-derived and synthetic cannabinoids are considered controlled substances subject to United States’ Federal Controlled Substances Act of 1970 (the “CSA”) and regulations promulgated thereunder, except hemp containing less than .3% THC and cannabinoids derived therefrom to the extent cultivated and produced in accordance with the Agriculture Improvement Act of 2018 (the “2018 Farm Bill”) (“Exempt Hemp Products”). See “Government Laws and Regulations” below. At present, TOP intends to focus on research and development of potential pharmaceutical products based on compounds derived from the TOL’s proprietary strains. Due to the early stage of TOP’s business, its inexperience, and the current status of cannabis as a Schedule I controlled substance in the United States, which under the CSA makes it unlawful to manufacture, distribute, dispense or possess, TOP has not commenced active development of or any clinical trials with respect to any pharmaceutical products in the United States.

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Rather, TOP and TOL have conducted all research to date in Israel. In light of the difficulty in proceeding with clinical trials in the United States, TOP intends to continue its drug development activities in jurisdictions, including Israel, with more favorable laws and regulations regarding research utilizing plant-derived cannabinoids.

Although TOP has not yet developed any pharmaceutical products, it has exclusive access to TOL’s cannabis strains and database of Israeli medical cannabis patients, which contains important patient and treatment data which it expects will serve as a platform which it can utilize to establish products that TOP believes will be effective to treat specific diseases. TOP intends to continue to collaborate with TOL to further develop new products subject to the required approval of various jurisdictions. In addition, TOP may enter into joint ventures or sublicense the TOL intellectual property or license any intellectual property it may develop, as may be applicable, to more established pharmaceutical companies or other third parties.

TOP plans to invest significant capital and professional efforts in the development of cannabinoid-derived pharmaceuticals with the ultimate objective of obtaining approval by the FDA, the European Medicines Agency (“EMA”) and from regulatory authorities in other countries and regions (the “Other Agencies”).

TOP’s drug development strategy incorporates the following general steps:

•

determination of diseases, disorders and medical conditions that could potentially benefit from cannabinoid-based drugs;

•

conducting “freedom to operate” investigations on these conditions;

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preparation of patent applications and securing such applications and/or the licensing of existing patents;

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identifying the regulatory pathway with the FDA, the EMA and Other Agencies;

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conducting pre-clinical studies;

•

submitting Investigational New Drug (“IND”) applications to the FDA and similar required applications to EMA and/or Other Agencies

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proceeding with pre-clinical studies and/or proof of concept trials, and clinical trials under the protocols for submission and obtaining approval for the particular drug development project(s) as required by the FDA, EMA or Other Agencies; and

•

Submitting a New Drug Application (“NDA”) to the FDA and similar required applications to EMA and/or Other Agencies.

TOP operates in a highly-controlled regulatory environment with strict regulations and established requirements by the FDA, EMA and Other Agencies, relating to analytical, toxicological and clinical standards and protocols with respect to the research and development of pharmaceuticals. Regulations specifically cover research, development, manufacturing and reporting procedures, both pre- and post-approval.

Governmental authorities in many countries require that a new pharmaceutical product be approved or exempted from approval before any such pharmaceutical product can be marketed. The time to obtain approval varies by country and some pharmaceutical drugs may fail in pre-clinical or clinical trials and therefore may never be approved. The approval process is typically a lengthy process that requires conducting pre-clinical studies and clinical trials to seek and then hopefully receive regulatory approval, in compliance with applicable statutes and regulations, and the expenditure of substantial capital resources.

The steps required to obtain approval and the commercialization of a new drug in the United States are lengthy, complex and expensive, and the outcome is far from certain. These steps generally include:

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completion of formulation studies, preclinical studies, and animal studies in compliance with the FDA’s good laboratory protocols (“GLP”);

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submission to the FDA of an IND to support clinical trials in the United States;

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approval by an Institutional Review Board (“IRB”) before each trial may be initiated;

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performance of controlled clinical trials in accordance with FDA regulations and with current good clinical practice (“GCP”) to establish the safety and efficacy of the drug candidate for each target indication;

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if clinical trials show that a therapeutic candidate is safe and effective, submission of NDA to the FDA;

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satisfactory completion of an FDA inspection of the manufacturing facilities at which the drug will be produced to assess compliance with current good manufacturing practices (“GMP”), and to assure that the facilities, methods and controls are adequate; and

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FDA review and approval of the NDA.

If a drug, such as those contemplated by TOP, contains a controlled substance under the CSA and is categorized in Schedule I, II, or III, it will likely require scheduling by the DEA prior to any potential commercialization, which may never be achieved. This step may be required for drugs containing plant-derived cannabinoids other than Exempt Hemp Products, as well as synthetic cannabinoids.

TOP has established the following two wholly owned subsidiaries:

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TO Pharmaceuticals USA LLC, a Delaware limited liability company (“TOPUSA”), which was formed to operate TOP’s business in the United States and to hold any United States patents issued in connection with TOP’s business; and

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Tikun Olam IP Ltd., a Cayman Islands entity (“TOIP”), which was formed to operate TOP’s business anywhere in the world excluding the United States and to hold all patents issued in any country other than the United States.

TOP’s Relationship with TOL

TOP has developed a strategic relationship with TOL to benefit from the industry experience and expertise of TOL as a foundation for TOP’s business. TOP has entered into license agreements with TOL in order to leverage TOL’s intellectual property, including its proprietary genetics, trademarks, tradenames and products.

Tikun Olam is Hebrew for “Repairing the World” and is defined by acts of kindness performed to perfect, heal or repair the world. TOP believes that TOL is one of the first large-scale nationally licensed producers and distributors of medical cannabis in the world, has set the global standard for non-pharmaceutical medical cannabis research and is one of the leading medical cannabis companies in the world. Founded in 2005 by philanthropist Tzachi Cohen with products tested by Prof. Rafael Mechoulam at Hebrew University, TOL received the first government-issued license to supply medical cannabis in the State of Israel. TOP believes that TOL is a major participant in the Israeli market, and as of 2017 was reported to be supplying approximately one-third (1/3) of that nation’s 32,000 medical cannabis patients.

Over the last ten years, TOL has tracked those patients’ progress over time, based on the consistent and documented use of specific strains. TOP believes that this data is beneficial because such extensive data may be shared with scientists, physicians, hospitals, and collaborators for a variety of purposes, which may include prescribing or recommending particular strains of cannabis for patients with certain conditions, further research studies and the development of products.

TOL’s most well-known strain is Avidekel, a high-CBD and lower-THC variety with little or no psychoactive effects. Avidekel is expected to serve as the basis for CBD-based products to be developed by TOP.

By collaborating with TOL, the Company has been able and intends to continue to use TOL’s extensive experience in the medical cannabis industry, including its extensive database of medical cannabis patients, which TOP expects will continue to serve as a platform for further research studies and clinical trial products.

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TOP’s Research and Development Strategy

Our current focus is on research and development of formulations for the treatment of specific medical conditions, diseases and/or disorders described more fully below.

Product Pipeline

TOP’s business is focused on research and development of potential pharmaceutical products based on compounds derived from TOL’s proprietary strains. In connection with its business, TOP endeavors to discover, develop and commercialize new pharmaceutical drugs and treatments, including by exploiting TOL’s proprietary cannabinoid derivative product database, subject to approval by the FDA, the EMA and/or Other Agencies. TOP collaborates or intends to collaborate with TOL and leading medical experts at major Israeli and European and/or US hospitals and research organizations in drug development and clinical research. To date, all pre-clinical and clinical trials conducted by or on behalf of TOP have been conducted in Israel. Accordingly, the data from these studies may not be applicable to any NDA filed with the FDA. To achieve its goal, TOP has initially focused its research and development efforts on the following diseases and symptoms:

Crohn’s and Colitis

Inflammatory bowel disease (“IBD”) is a chronic autoimmune condition where parts of the digestive system become sore and inflamed. The disease can lead to irreversible damage to the gastrointestinal tract and require surgical removal of the intestine and affected areas. Two major forms of the disease are Crohn’s disease, which can affect any part of the digestive system, and ulcerative colitis, which often affects the rectum and the colon or the large intestine. IBD is a chronic condition, meaning that it is ongoing and typically lasts throughout life in those that are afflicted. The disease is often unpredictable, and there are periods of remission where there are few or no symptoms, which alternate with periods where symptoms are very active and debilitating. The peak incidence of IBD onset occurs between the ages of 15 and 30 years. Clinicians caring for children and adolescents afflicted with pediatric IBD must treat the underlying disease while also monitoring growth, puberty, and cognitive development, while seeking to minimize hospitalization time.

Therapies for IBD include anti-inflammatory therapies, immune system suppressors, antibiotics and surgical interventions. Anti-inflammatory therapies emerged as the largest therapy type segment for IBD in 2016 due to efficacy. Immune system suppressors emerged as the fastest growing segment due to reduction in surgeries and hospitalization rates. Approximately 1.86 billion patients have been diagnosed with IBD globally, with 1.54 billion patients currently receiving treatment. Increasing awareness of the disease, coupled with rising initiatives by regulatory bodies for development of novel treatment options, is estimated to provide the market with high growth potential. Traditional therapies, including products provided by Johnson & Johnson Services Inc., Pfizer Inc., Allergan and AbbVie Inc., have yielded $4.18 billion in annual sales around the world, which is expected to increase to $6.85 billion by 2022 with the approval of various pipeline drugs, according to Global Data’s Global Drug Forecast and Market Analysis to 2022.

TOP has entered into a clinical trial agreement dated April 28, 2017, (the “MOR Agreement”) with Prof. Timna Naftali (“Naftali”) and MOR Research Applications Ltd., an Israeli company (“MOR”) which is also the technology transfer company of Clalit Health Services (“Clalit”) and legal and authorized representative of Clalit and the Meir Hospital (Israel) (“Meir”), with respect to the commercialization of intellectual property that is developed by Clalit’s and Meir’s employees. The purpose of the MOR Agreement is to examine and use Avidekel, a proprietary cannabis plant of TOL to which TOP holds intellectual property rights, with respect to the treatment of patients with IBD, and in particular to conduct a randomized, placebo-controlled study to assess the benefit of Avidekel oil in patients with Crohn’s disease and achieve a written study that can be utilized to create an IBD-based treatment or drug approved by the applicable drug administration(s). In this study, approximately 50 patients were administered an oral dosage of oil containing Avidekel, while the control group was administered a placebo carrier oil without the active ingredients. Pursuant to the MOR Agreement, (a) TOP is obligated to pay to MOR (i) for the 80 subjects taking part in this study, an amount of US$120,000 (US$1,500 per subject), and (ii) an annual amount equal to 8% of TOP’s net revenues generated and actually received by TOP from the sale of the IBD drug to the public for the treatment of IDB; and (b) TOP retains all right, title and interest in and to all intellectual

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property and derivatives, modifications, enhancements and improvements thereto. The administration of this study has been completed and the results are awaiting final analysis. TOP expects Phase 2 trial results from this study to be announced in first quarter of 2019.

The primary endpoint of the study was measurement of reduction in Crohn’s Disease Activity Index CDAI Score of at least 100 after 8 weeks of treatment. Secondary efficacy endpoints included:

(i)

disease remission (CDAI drop of 150+)

(ii)

improvement of at least one point in Endoscopic disease activity index

(iii)

improvement of CRP and calprotectine

(iv)

improvement of blood cytokine levels and improved colonoscopy data.

Alzheimer’s Disease and Dementia

According to the Alzheimer’s Association, dementia is not a specific disease. It is an overall term that describes a group of symptoms associated with a decline in memory or other thinking skills severe enough to reduce a person’s ability to perform everyday activities. Alzheimer’s disease (“AD”) is reported to account for 60 to 80 percent of cases. Vascular dementia, which occurs after a stroke, is the second most common dementia type. There are many other conditions that can cause symptoms of dementia, including some that are reversible, such as thyroid problems and vitamin deficiencies. Dementia is caused by damage to brain cells, which damage interferes with the ability of brain cells to communicate with each other. When brain cells cannot communicate normally, thinking, behavior and feelings can be affected. People with dementia typically may have problems with short-term memory, keeping track of a purse or wallet, paying bills, planning and preparing meals, remembering appointments or traveling out of the neighborhood.

According to the Alzheimer’s Association, approximately 5.7 million people in the United States are living with AD, approximately half of which are diagnosed. Studies suggest that 40 – 50 percent of patients diagnosed with AD in the United States exhibit agitation. According to business information and analytics company GlobalData, the global AD market was $2.9 billion in 2016, and is predicted to reach $14.8 billion by 2026 across the U.S., Japan, France, Germany, Italy, Spain, and the UK, the seven major markets, reflecting an annual growth rate of 17.5%. Leading pharmaceutical companies in the AD drug market include Allergan plc and Novartis AG, which have expanded their global market presence through acquisitions of emerging brands. Other key players in the global AD drugs market include H. Lundbeck A.S., Eisai Co. Ltd., Daiichi Sankyo Company Limited, Merz Holding GmbH & Co KG., Ono Pharmaceutical Co. Ltd. and Johnson & Johnson.

TOP has entered into a clinical trial agreement dated August 15, 2017, (the “Lanaido Agreement”) with Dr. Hermush Vered (“Vered”) and Lanaido Hospital, an Israeli company (“Lanaido”) which is also the hospital at which Vered practices. Pursuant to the Lanaido Agreement, Lanaido, under the supervision of Vered, is conducting a randomized placebo-controlled study focused on evaluating the safety and efficacy of Avidekel oil for the treatment of subjects with agitation related to Alzheimer’s and other forms of dementia. Pursuant to the Lanaido Agreement, (a) TOP is obligated to pay to Lanaido $115,000; (b) TOP retains all right, title and interest in and to all intellectual property subject to the Lanaido Agreement; and (c) TOP is permitted to publish the results of and information pertaining to the study, whether, for any scientific, commercial or promotional purposes, at any time. TOP is currently in the process of enrolling approximately 60 patients in this study, who will be administered an oral dosage of oil containing Avidekel, while the control group will be administered a placebo carrier oil without the active ingredients. This administration is underway. TOP expects this Phase 2 Trial to be completed in the third quarter of 2019.

The primary efficacy endpoint of the study is the analysis of the proportion of subjects achieving a decrease of four points or more in Cohen-Mansfield Agitation Inventory (CMAI) during the treatment period at week sixteen compared to baseline starting point. Secondary efficacy endpoints include:

(i)

Assessment of the proportion of subjects achieving a CMAI ≥ 4-point decrease during the treatment period at each time point.

(ii)

Time to 4-point reduction in CMAI in treatment as compared to the control group.

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(ii)

Mean change in CMAI score.

(iv)

Mean change in Neuropsychiatric Inventory (NPI-NH) agitation/aggression sub-score.

Migraine and Headache

According to the American Migraine Foundation, a migraine is an episodic, unpredictable headache disorder that presents with disabling attacks. These migraine attacks may be successfully treated with acute medications. At present, some of these medications are available over the counter and are prescription medications. Acute medications fall into general classes of medicines including analgesics, ergotamines, and triptans.

In the U.S., more than 38 million people suffer from migraines. Some migraine studies estimate that 13% of adults in the U.S. population have migraines, and 2 – 3 million migraine suffers are chronic. According to a 2018 report by Grand View Research, Inc., the global migraine drug market size is expected to be approximately $7.8 billion by 2025, reflecting an 18.0% CAGR during the forecast period. TOP believes that this market is driven primarily by a rise in disease prevalence, development of novel therapies, lifestyle changes, and hormonal medications.

The global migraine drugs market has been mainly dominated by usage of generic triptans and other off-label drugs. Many currently prescribed drugs for both acute symptoms and preventative treatment are associated with poor efficacy and unfavorable side-effects. Amgen and Novartis have launched a new CGRP-based drug for migraines, Aimovig and Teva Pharmaceutical Industries Ltd.’s has also introduced its product Ajovy, which may significantly alter the treatment of migraine prevention. TOP anticipates that drug manufacturers such as Eli Lilly, Alder BioPharma, and Biohaven Pharma are likely to enter the market by 2019, and also believes that pricing will be a key differentiating factor as all CGRP-based therapies have a similar efficacy and safety profile.

TOP has entered into a clinical trial agreement dated December 21, 2017 (the “Soroka Agreement”) with Prof. Gal Ifergane (“Ifergane”) and Clalit through Soroka University Medical Center, an Israeli company (“Soroka”). Pursuant to the Soroka Agreement, Soroka, under the supervision of Ifergane, is conducting a randomized placebo-controlled study in order to assess the safety and efficacy of medical grade cannabis oil derived from the cannabis strain Erez in acute migraine patients. Pursuant to the Soroka Agreement, (a) TOP is obligated to pay to Soroka an amount equal to US$200,000, which is due in installments based upon the achievement of certain thresholds, including a fee per subject of US$1,927 for up to 88 subjects, (b) TOP retains all right, title and interest in and to all intellectual property subject to the Soroka Agreement; and (c) TOP is permitted to publish the results of and information pertaining to the study, whether, for any scientific, commercial or promotional purposes, at any time. TOP is currently enrolling approximately 60 patients in this study, who will be administered an oral dosage of oil containing Erez, while the control group will be administered a placebo carrier oil without the active ingredients. This administration is underway.

TOP expects that this Phase 2 trial will be completed in the first half of 2019.

Primary efficacy endpoint of the study is treatment success defined as headache pain relief resulting in improvement of at least two levels in migraine severity from baseline starting point within two hours after treatment initiation. Secondary efficacy endpoints include:

(i)

Patient global assessment at 2 hours, 4 hours and 24 hours after investigational product consumption.

(ii)

Overall satisfaction level at 2 hours, 4 hours and 24 hours after investigational product consumption.

(iii)

Pain relief: the percentage of patients with a reduction of headache severity from moderate or severe at baseline to mild or none at 2 hours.

(iv)

Pain free: the percentage of patients with a reduction of headache severity from moderate or severe at baseline to none (i.e. complete abolition of headache) at 2 hours.

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PEW in Hemodialysis

Hemodialysis-related protein-energy wasting (“PEW”) is common in patients with chronic kidney disease (“CKD”). PEW is one of the strongest predictors of mortality in patients with CKD. The International Society of Renal Nutrition and Metabolism (ISRNM) expert panel has defined PEW as a “state of decreased body stores of protein and energy fuels (body protein and fat masses)”. The ISRNM panel has also proposed diagnostic criteria of PEW with four categories. Cachexia is a severe form of PEW. The proposed causes of PEW are multi-factorial and include nutritional and non-nutritional mechanisms.

According to statistics by the National Kidney Foundation, as of 2018, there were more than 2 million people across the globe suffering from chronic kidney failure who are currently undergoing dialysis as an alternative treatment provided until renal transplantation is available. Even though the transplant percentages are rising each year, the dialysis rate remains relatively constant, due to the identification of new cases of diabetes and renal disorders such as kidney failure and chronic renal dysfunction. According to Grand View Research, the global hemodialysis and peritoneal dialysis market was $60.6 billion in 2017 and is expected to grow to $108.5 billion at a CAGR of 6.0% though 2025.

TOP has entered into a clinical trial agreement dated June 20, 2018 (the “Assaf Harofeh Agreement”) with Dr. Ilia Beberashvili (“Beberashvili”) and Medical Research and Development Fund for Health Services-Assaf Harofeh Medical Center (“Assaf Harofeh”), an Israeli company (“Assaf Harofeh”). Pursuant to the Assaf Harofeh Agreement, Assaf Harofeh, under the supervision of Beberashvili, is conducting a randomized, double-blind, placebo controlled, parallel-group, pilot study in order to investigate the safety and efficacy of medical grade cannabis oil derived from the strain Midnight in maintenance hemodialysis patients with PEW. Pursuant to the Assaf Harofeh Agreement, (a) TOP is obligated to pay to Assaf Harofeh an amount equal to US$137,000, (b) TOP retains all right, title and interest in and to all intellectual property subject to the Assaf Harofeh Agreement; and (c) TOP is permitted to publish the results of and information pertaining to the study, whether, for any scientific, commercial or promotional purposes, at any time. In this study, approximately 40 patients will be enrolled and administered an oral dosage of oil containing Midnight, while the control group will be administered a placebo carrier oil without the active ingredients. This study has been approved by Israeli authorities and TOP expects to begin enrolling patients in 2019. TOP expects this Phase 2 trial to be completed in the second half of 2019.

The primary efficacy endpoint of the study is treatment success defined as safety and tolerability after single and multiple oral doses in adult maintenance hemodialysis MHD patients and assessment of the effect on the appetite of adult patients on maintenance hemodialysis. Secondary efficacy endpoints include:

(i)

characterizing the pharmacokinetic profile of the Midnight cannabis oil (and its metabolites) after single and multiple oral doses;

(ii)

evaluating the effect nutritional scores (MIS, GNRI, OSND) in the study population;

(iii)

evaluating the effect on health-related quality of life in the study population; and

(iv)

evaluating the effect on muscle strength.

Additional Research and Development

TOP has entered into a clinical trial agreement dated June 6, 2018 (the “Sheba Agreement”) with Prof. Guy Ben Simon (“Simon”) and The Sheba Fund for Health Services and Research (R.A.), an Israeli company (“Sheba Fund”). Pursuant to the Sheba Agreement, the Sheba Fund, under the supervision of Simon, is conducting a study in order to assess the use of THC in medical grade cannabis oil derived from the strain Erez in connection with a certain indication. Pursuant to the Sheba Agreement, (a) TOP is obligated to pay to Sheba Fund an amount equal to US$61,000, which is due on a per subject and per visit basis for up to 20 subjects, (b) TOP retains all right, title and interest in and to all intellectual property subject to the Sheba Agreement; and (c) TOP is permitted to publish the results of and information pertaining to the study, whether, for any scientific, commercial or promotional purposes, at any time. TOP expects this Phase 2 trial to be completed in fourth quarter of 2019.

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Market Opportunities

Many pharmaceutical and biotechnology companies are seeking to capitalize on the anticipated growth in the pharmaceutical market for cannabinoid-based drugs by realizing and leveraging the growing set of data on the therapeutic effects of cannabis and cannabinoids. TOP believes that the potential applications for cannabinoids go beyond the three cannabinoid-based drugs derived from isolated synthetics: Marinol, Syndros and Casamet, that have been approved by the FDA to date. Cannabinoid-based drug candidates typically use CBD and THC, or a combination thereof, as their active ingredient(s). TOP, with the cooperation of TOL, has been conducting pre-clinical trials and randomized, placebo-controlled clinical trials on TOP’s products, each in Israel, using cannabinoid-based compounds to develop unique, condition-specific formulas, with the goal of ultimately commencing FDA-approved trials in the United States and EMA-approved trials in Europe.

In June 2018, the FDA approved Epidiolex, a cannabidiol (CBD) oral solution for the treatment of seizures associated with two rare and severe forms of epilepsy, Lennox-Gastaut syndrome and Dravet syndrome, in patients two years of age and older. This is the first FDA-approved drug that contains a purified drug substance derived from cannabis. It is also the first FDA approval of a drug for the treatment of patients with Dravet syndrome. TOP believes that this approval creates a precedent with FDA for similar drug substances derived from cannabis.

TOP believes that it is likely that the pharmaceutical market for cannabinoid-based drugs will eventually be classified as part of the specialty pharmaceutical market. The increasing diagnoses of certain chronic diseases has resulted in an increased need for specialty drugs. According to a 2017 report published by the HDA Research Foundation, “Specialty Pharmaceutical Distribution: Facts, Figures and Trends (2017 Edition),” spending on specialty drugs in 2016 in the U.S. was about $181 billion and estimated projections suggest that spending on specialty drugs may grow by 2020 to $300 billion to $400 billion.

Cannabinoids have a diverse pharmacology which TOP believes could provide significant potential for therapeutic applications across many diseases, disorders and medical conditions in areas that define specialty pharmaceutical drugs. TOP believes that spending on drug development projects in the cannabinoid-based pharmaceutical market sector could represent 5% of the overall specialty pharmaceutical market by the year 2020, which would suggest a market size of around $20 billion. According to Statista, an online statistic, market research and business intelligence portal that provides access to data from market and opinion research institutions, the U.S. market for cannabinoid-based pharmaceuticals will increase to $50 billion by 2029. TOP believes these estimates are reasonable given the significant amounts of capital that have been allocated for the development of cannabinoid-derived pharmaceuticals by numerous companies in the U.S. and globally, with the objective of obtaining regulatory approval by the FDA, EMA and other agencies. TOP believes that there will be rising demand for cannabinoid-derived drugs and that future growth is likely to be driven by favorable changes in legislation and demographic factors. Controlled substance laws differ between countries and legislation in certain countries may restrict or limit TOP’s ability to distribute or sell its drugs. TOP believes that the U.S. will represent a major market for TOP’s cannabinoid-based drug candidates. In the European Community, all medical cannabis products are currently considered pharmaceutical products. Several medical cannabis program regulatory frameworks exist in countries, including the Netherlands, Italy, Germany, Finland and the Czech Republic, and TOP anticipates that there will be policy changes in these and many member countries of the European Union regarding the medical use of cannabinoid-derived drugs, though no assurance can be given in this regard.

Over 160 chemical compounds have been isolated from the cannabis plant. The most common are CBD and THC. CBD and THC are believed to interact with CB1 and CB2 receptors, which are located throughout the human body. CB1 receptors are primarily located in the brain and central nervous system. CB2 receptors are located throughout the body including on immune processing cells, peripheral nerves and joint tissues and the gastrointestinal and urinary tracts that are responsible for regulating neurotransmission. The CB1 and CB2 receptors help control bodily reactions such as inflammation and pain, which are areas are of significant therapeutic interest with respect to drug development. Identifying cannabinoid receptors and the compounds that interact with them has helped accelerate clinical investigations of cannabinoid-based drugs.

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Endogenous cannabinoid receptors are present in the human central nervous system (“CNS”) and in peripheral sites. Two main endogenous cannabinoids are Anandamide (“AEA”) and 2-Arachydonilglyerol (“2-AG”). Both are synthesized on cell membrane phospholipids and activate neuronal pre-synaptic receptors, CB1 and CB2. AEA and 2-AG, the enzymes that synthesize and degrade them and the CB1 and CB2 receptors, constitute the human endocannabinoid system.

TOP believes cannabinoid-based drugs may provide a superior treatment model for patients suffering from certain diseases, disorders and medical conditions. To date, due to the challenges of researching plant-derived cannabinoids in the United States, including FDA and DEA restrictions, most U.S. research has been conducted utilizing synthetically produced cannabinoids, which as chemical compounds, are chemically identical to plant-derived cannabinoids. At present, there are two synthetic “THC” cannabinoids available, dronabinol and nabilone. Both have been approved in the U.S. for the treatment of nausea and vomiting associated with cancer chemotherapy in patients who have not responded adequately to conventional antiemetic treatments. Dronabinol capsules were also approved for treatment of anorexia associated with weight loss in patients with acquired immune deficiency syndrome, or AIDS. They are also often prescribed for pain control, as alternatives to opioids

Patents, Intellectual Property and Proprietary Rights

TOP has sought and intends to continue to seek patent protection in the U.S. and other countries, as appropriate, related to methods and compositions and proprietary technologies for the use of cannabinoids and cannabis-based compositions and methods for the treatment of certain diseases, disorders and medical conditions.

To date, TOP has filed five provisional patent applications with the USPTO, all related to the use of cannabinoids and/or cannabis-based compositions and methods to treat certain diseases, disorders or medical conditions. Assuming the successful completion of clinical trials, of which there can be no assurance, TOP believes that it will be able to secure patent protections and retain the intellectual property rights relating thereto. The table below sets forth TOP’s provisional patent applications:

Application number	Description of Provisional Patent	Filing Date
62/610,589	Use of cannabinoid compositions for the treatment of inflammatory skin disorders*	December 12, 2017
62/632,021	Use of cannabinoid compositions and methods for the treatment of protein energy wasting	February 19, 2018
62/674,235	Use of cannabinoid compositions for the treatment of inflammatory skin disorders	May 21, 2018
62/676,093	Use of cannabis-based compositions for the treatment of autistic spectrum disorders	May 24, 2018
62/776,076	Use of cannabis-based compositions for the treatment of Alzheimer’s disease and dementia	December 6, 2018
62/776,084	Use of cannabis-based compositions for the treatment of Migraine and headache	December 6, 2018

Sublicensed pursuant to the JP Sublicense Agreements (as defined below).

In addition:

•

on November 2, 2017, TOP filed a patent application under the Patent Cooperation Treaty, published May 11, 2018 (WO 2018/083697), relating to the methods of using of CBD and glatiramer acetate (“GA” or “copaxone”) for treating, preventing, ameliorating or delaying multiple sclerosis, and side effects associated with multiple sclerosis treatment.

•

on November 2, 2017, TOP filed a patent application under the Patent Cooperation Treaty, published May 11, 2018 (WO 2018/083695), relating to methods and formulations utilized in the methods which comprise cannabis plant extracts and copaxone.

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•

on March 28, 2017, TOP filed a patent application under the Patent Cooperation Treaty, published October 5, 2017 (WO 2017/168422), relating to compositions and methods for treating inflammatory condition of the gastrointestinal (“GI”) tract, specifically those related to Inflammatory Bowel Disease (“IBD”). Compositions according to this invention, due to their specific content of cannabinoids and methods comprising specific modes of administration thereof, are particularly applicable to the treatment of the two major IBDs, Crohn’s disease and colitis.

TOP seeks patent protection for the technology, inventions and improvements that it considers important to the development of its business, but only in those cases where TOP believes that the costs of obtaining patent protection is justified by the commercial potential of the drug candidate and/or proprietary technologies, and typically only in those jurisdictions that it believes present significant commercial opportunities. The commercial success of TOP will depend in part on obtaining and maintaining patent protection and trade secret protection for its drug candidates, and successfully defending these patents against third-party challenges. TOP’s ability to protect its drug candidates from unauthorized making, using, selling, offering to sell or importing by third parties is dependent on the extent to which it has rights under valid and enforceable patents that cover these activities.

U.S. and Worldwide Pharmaceutical Licenses with TOL

Pursuant to a 2015 binding memorandum of understanding (the “MOU”) between an equityholder of the Company’s parent (until July 13, 2018) and TOL, (i) TOP’s wholly owned subsidiary TO Pharmaceuticals USA LLC, a Delaware limited liability company (“TOPUSA”) entered into a license agreement dated as of April 13, 2017, as amended (the “US Pharma License”) with TOL relating to TOP’s U.S. pharmaceutical business (the “U.S. Pharmaceutical Business”); and (ii) TOP’s wholly owned subsidiary Tikun Olam IP Ltd., a Cayman Islands entity (“TOIP”) and TOL entered into a license agreement dated as of April 13, 2017, as amended (the “WW Pharma License”, and together with the US Pharma License, the “Pharma Licenses”) relating to TOP’s non-U.S. pharmaceutical business (the “Worldwide Pharmaceutical Business”; and together with the U.S. Pharmaceutical Business, the “Pharmaceutical Business”). Pursuant to the Pharma Licenses, TOL granted an exclusive, perpetual, non-revocable, royalty-free and sublicensable license to use TOL’s intellectual property, whenever developed, in connection with TOP’s Pharmaceutical Business. TOPUSA is permitted to use such intellectual property solely in the United States and TOIP is permitted to use such intellectual property anywhere in the world excluding the United States.

Each of TOPUSA and TOIP will own all intellectual property and improvements and modifications of TOL’s intellectual property relating to the Pharmaceutical Business that is developed or acquired collaboratively with TOL or solely by TOPUSA or TOIP, as applicable (collectively, the “New IP”). Each of TOPUSA and TOIP have the right to use all New IP in connection with the Pharmaceutical Business, including sublicensing such New IP to third-parties. Further, if any clinical trials are conducted solely by TOPUSA or TOIP, as applicable, or in collaboration with TOL, then the results of such clinical trials and all intellectual property in connection with such trials, are owned by TOPUSA or TOIP, as applicable. Each of TOPUSA and TOIP are required to grant to TOL a perpetual, non-revocable, royalty-free, non-exclusive and sublicensable license to New IP, any new strains developed during the term of the Pharma Licenses and the results of such clinical trials, including any improvements and modifications thereof by TOPUSA or TOIP, as applicable, or any other party expect TOL, in each case solely in connection with TOL’s cannabis business.

Pursuant to the MOU, TOPUSA, TOIP, or an affiliate, has paid or caused to be paid to TOL an aggregate of two million five hundred thousand U.S. Dollars ($2,500,000), of which $500,000 was paid to TOL on behalf of TOPUSA and TOIP. Full payment was made to TOL by or on behalf of each of TOPUSA and TOIP and their affiliates, and no royalties or other payments are required under the Pharma Licenses, except a two percent (2%) royalty payable to TOL with respect to TOIP’s sale of over-the-counter pharmaceutical products outside the U.S. which reasonably compete with a non-pharmaceutical medical cannabis product with substantially similar composition of active components sold by TOL or any licensee of TOL (other than TOIP) conducting business in the applicable jurisdiction pursuant to an effective legal license, permit or similar authority.

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The Pharma Licenses also provide that TOL (i) is not permitted to operate or license the intellectual property of TOL to any third party with respect to the Pharmaceutical Business anywhere in the world; (ii) TOL is required to continue to conduct research and development efforts, provide training and assistance with research and development, provide design and operations services, and assist in conducting clinical studies or trials; (iii) is required to expend certain additional funds, which it has expended, to enhance the TOL intellectual property; and (iv) is required to pay an amount equal to one-half of the costs and expenses relating to any infringement or threatened infringement action by a third-party which TOPUSA or TOIP, as applicable, takes reasonable action to stop or otherwise enforce its rights, provided, that such amount shall not exceed an aggregate of US$200,000 (the “Cap”). If the Cap is exceeded, then TOL shall nevertheless participate in and contribute towards, such costs, solely by means of offset against any royalties (“TOLLC Royalties”) due to TOL under a license agreement with an affiliate of TOP (“TOLLC”) (the “TOLLC License”), in amounts based on percentages of certain TOLLC Royalty thresholds.

With respect to TOL-owned trademarks, trade names and similar intellectual property, whether registered, under application for registration or not, together with the goodwill relating thereto (“TOL Marks”), all rights therein and any goodwill accruing during the term of the Pharma Licenses belongs to TOL. Further, each of TOPUSA and TOIP is not permitted to misuse or misappropriate any TOL Marks or take any other conduct that impairs or might tend to impair the validity or enforceability of any TOL Marks or registrations in connection with such TOL Marks. Each of TOPUSA and TOIP is required to affix all pharmaceutical products subject to the respective Pharma License and any related promotional and packaging materials with such Marks and any notices reasonably requested by TOL. TOL has the right, upon no less than fifteen business days prior written notice to TOPUSA or TOIP as applicable, to inspect the premises, books and records of TOPUSA or TOIP, in order to verify TOPUSA or TOIP, as applicable, is in compliance with the respective Pharma License and appropriate quality control as it relates to the TOL Marks. Each Pharma License also contains mutual indemnification, confidentiality obligations and non-competition covenants. Such non-competition covenants cover the term of the agreement and a period of twelve months after the termination or cancellation of the respective Pharma License.

Tikkun Pharma Sublicenses

TOPUSA has entered into an exclusive amended and restated sublicense agreement with Tikkun Pharma, Inc., a Delaware corporation (“Tikkun Pharma”), dated as of September 11, 2017 (the “TP USA Sublicense Agreement”), and TOIP has entered into an exclusive amended and restated sublicense agreement with Tikkun Pharma, dated as of September 11, 2017 (the “TP WW Sublicense Agreement”; and together with the TP USA Sublicense Agreement, the “TP Sublicense Agreements”), pursuant to which TOPUSA and TOIP each have granted a perpetual, non-revocable (subject to the terms of the TP Sublicense Agreements), fully paid, royalty-free, exclusive sublicense of TOL’s intellectual property and license of their respective intellectual property, in their respective territories, in connection with the production, research, development, promotion, marketing, sale, distribution and commercialization of pharmaceutical products derived from such intellectual property as it relates to the prevention, management and treatment of cancer or autoimmune diseases, disorders or symptoms related thereto, other than (1) Crohn’s Disease, coeliac diseases, any type of colitis (including without limitation microscopic and ulcerative colitis), any and all digestive and IBD, together with any diseases, disorders or symptoms related thereto, and (2) all diseases and disorders, and symptoms thereof, using glatiramer acetate (also known as Copaxone), whether alone or in a combination with any product, including not limited to, CBD (the “TP Limited Business”).

Pursuant to the TP Sublicense Agreements, TP is obligated to prepare, in consultation with TOP, and provide to the board of directors of Tikkun Pharma, a mutually acceptable commercialization plan covering the development and commercialization of the intellectual property subject thereto, which shall include, among other things, (1) a list of appropriate studies with specific cannabis-related indications and deadlines for initiating one or more such studies, and (2) a list of one or more inventions for which patent rights should be pursued, if appropriate. All improvements and modifications of TOL’s and TOP’s intellectual property relating solely to the TP Limited Business developed or acquired by Tikkun Pharma will be owned by Tikkun Pharma; provided, that Tikkun Pharma will grant to TOP a perpetual, royalty-free, non-exclusive license to use and exploit such intellectual property. To the extent this is not

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permissible under any license agreement with TOL, such intellectual property will be assigned to TOP or TOL as required by such license agreement.

With respect to TOL-owned trademarks, trade names, logos service marks, designs, emblems, signs, slogans, other similar designations of source or original and general intangibles of like nature, whether registered, under application for registration or not, together with the goodwill relating thereto (“Sublicensed Marks”), all rights therein and any goodwill accruing during the term of the TP Sublicense Agreements belong to TOL. Further, Tikkun Pharma is not permitted to misuse or misappropriate any Sublicensed Marks or any other conduct that impairs or might tend to impar the validity or enforceability of any Sublicensed Marks or registrations in connection with such Sublicensed Marks. Tikkun Pharma is required to affix all pharmaceutical products subject to the TP Sublicense Agreements and any related promotional and packaging materials with such Sublicensed Marks and any notices reasonably requested by TOP. TOP has the right, upon no less than fifteen business days prior written notice to Tikkun Pharma, to inspect the premises, books and records of Tikkun Pharma in order to verify Tikkun Pharma’s compliance with the TP Sublicense Agreement and appropriate quality control as it relates to the Sublicensed Marks.

Each of TOP and Tikkun Pharma have the right to immediately terminate each of the TP Sublicense Agreements upon the occurrence of a material breach of such agreement, subject to a thirty (30) calendar day cure period commencing after written notice by one party to the other, or the filing of a petition in bankruptcy by either TOPUSA or TOIP, respectively, or Tikkun Pharma, whether voluntary or involuntary, or if any petition, application or other pleading is filed or any proceeding is commenced seeking the appointment of a trustee, receiver or liquidator for the other party. The TP Sublicense Agreements also include mutual indemnification and confidentiality obligations. Tikkun Pharma has failed to fulfill certain of its obligations to TOP, with respect to which TOP has not exercised any remedial action.

Jay Pharma Sublicenses

TOPUSA has entered into an exclusive sublicense agreement with Jay Pharma, dated as of January 12, 2018 (the “JP USA Sublicense Agreement”), and TOIP has entered into an exclusive sublicense agreement with Jay Pharma, dated as of January 12, 2018 (the “JP WW Sublicense Agreement”; and together with the JP USA Sublicense Agreement, the “JP Sublicense Agreements”), pursuant to which TOPUSA and TOIP each have granted a perpetual, non-revocable (subject to the terms of the JP Sublicense Agreements), fully paid, royalty-free, exclusive sublicense of TOL’s intellectual property and license of their respective intellectual property, in their respective territories, in connection with the production, research, development, promotion, marketing, sale, distribution and commercialization of pharmaceutical products derived from such intellectual property as it relates to the prevention, management and treatment of cancer and diseases, disorders or symptoms related thereto (the “JP Limited Business”).

Pursuant to the JP Sublicense Agreements, Jay Pharma is obligated to prepare, in consultation with TOP, and provide to the board of directors of Jay Pharma, a mutually acceptable commercialization plan covering the development and commercialization of the intellectual property subject thereto, which shall include, among other things, (1) a list of appropriate studies with specific cannabis-related indications and deadlines for initiating one or more such studies, and (2) a list of one or more inventions for which patent rights should be pursued, if appropriate. All improvements and modifications of TOL’s and TOP’s intellectual property relating solely to the JP Limited Business developed or acquired by Jay Pharma will be owned by Jay Pharma; provided, that Jay Pharma will grant to TOP a perpetual, royalty-free, non-exclusive license to use and exploit such intellectual property. To the extent this is not permissible under any license agreement with TOL, such intellectual property will be assigned to TOP or TOL as required by such license agreement.

With respect to the Sublicensed Marks, all rights therein and any goodwill accruing during the term of the JP US Sublicense Agreements belong to TOL. Further, Jay Pharma is not permitted to misuse or misappropriate any Sublicense Marks or any other conduct that impairs or might tend to impar the validity or enforceability of any Sublicensed Marks or registrations in connection with such Sublicensed Marks. Jay Pharma is required to affix all pharmaceutical products subject to the JP Sublicense Agreements and any related promotional and packaging materials with such Sublicensed Marks and any notices reasonably

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requested by TOP. TOP has the right, upon no less than fifteen business days prior written notice to Jay Pharma to inspect the premises, books and records of Jay Pharma in order to verify Jay Pharma’s compliance with the JP Sublicense Agreements and appropriate quality control as it relates to the Sublicensed Marks.

Each of TOP and Jay Pharma have the right to immediately terminate the JP Sublicense Agreements upon the occurrence of a material breach of such agreement, subject to a thirty (30) calendar day cure period commencing after written notice by one party to the other, or the filing of a petition in bankruptcy by either TOPUSA or TOIP, respectively, or Jay Pharma, whether voluntary or involuntary, or any petition, application or other pleading is filed or any proceeding is commenced seeking the appointment of a trustee, receiver or liquidator for the other party. The JP Sublicense Agreements also include mutual indemnification and confidentiality obligations.

Competition

The emerging markets for cannabinoid-based drug research and development is and will likely remain competitive. In general, the biotechnology and pharmaceutical industries are characterized by rapidly advancing technologies, intense competition, and a strong emphasis on proprietary drugs.

TOP expects that it will be required to compete with a variety of multinational pharmaceutical companies and specialized biotechnology companies, as well as drugs and processes being developed at universities and other research institutions. TOP’s competitors may develop or may already have developed drugs comparable or competitive with TOP’s drug candidates. Competitive therapeutic treatments for diseases, disorders and medical conditions that are included in TOP’s drug development projects have already been approved and accepted by the medical community and any new treatments that may enter the market would face fierce competition. In addition to major pharmaceutical and biotechnology companies, such as the aforementioned competitors, TOP’s competitors also include public and private research institutions and several other U.S.-based companies that are in early stage discovery and preclinical development utilizing synthetic and/or plant-derived CBD and/or THC.

Currently, there are a number of large, well-established companies that are engaged in cannabinoid-based drug development. These include:

•

GW Pharmaceuticals, PLC, a United Kingdom company (NASDAQ: GWPH), has developed Epidiolex, which is pure plant-derived CBD and has been approved by the FDA for the treatment of Dravet syndrome, a form of childhood epilepsy. With respect to GW Pharmaceutical’s Sativex (nabiximols), a cannabis plant-derived formulation approved for the treatment of spasticity due to multiple sclerosis in numerous countries outside of the U.S., GW Pharmaceuticals has full commercial rights to this product and plans to meet with the FDA in the second half of 2018 to discuss data from its completed Phase 3 trials in Europe and to determine the optimal regulatory pathway in the U.S.

•

Arena Pharmaceuticals, Inc. (“Arena”), which is developing a synthetic selective CB2 receptor agonist for treatment of Crohn’s disease pain.

•

Insys Therapeutics, Inc. (NASDAQ: INSY), which in July 2016 obtained FDA approval for Syndros, an orally administered liquid formulation of dronabinol.

•

Nabilone, the first FDA approved synthetic THC drug, was originally developed by Eli Lilly & Company and received FDA approval in 1985. However, Eli Lilly withdrew that approval in 1989 for commercial reasons. Valeant Pharmaceuticals International Inc. (NYSE: VRX) acquired the rights from Eli Lilly in 2004 and the drug was approved again 2006.

•

Therapix Biosciences, Ltd., an Israeli corporation (NASDAQ: TRPX) is also exploring the use of THC plus palmidrol for Tourette Syndrome.

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Nexien Biopharma, Inc., a Delaware corporation, is a development stage biopharmaceutical company researching and developing cannabinoid-based formulations for the treatment of specific medical conditions, and/or disorders, which may include research and development as it relates to cannabinoid receptor modulators and/or terpenes in acute treatment situations during exposure to organophosphorus nerve agents and/or organophosphorus insecticides.

TOP believes that it has been able to and will continue to differentiate itself from its competitors because of, among other things, the following factors:

DATA

RESEARCH

CLINICAL DEVELOPMENT

•

TOL has amassed one of the largest medical cannabis treatment databases in the world, with over 20,000 patient records.

•

Patients have reported on the strain used, dosage prescribed and outcomes across a wide variety of diseases.

•

TOP has leveraged TOL’s data to selectively apply for 7 patents.

•

TOP and TOL scientists have been researching cannabinoids for over 40 years.

•

At least ten published peer-reviewed journal articles have been published by the TOP and TOL team.

•

TOP and TOL regularly conduct retrospective analyses on its patient dataset to identify optimal strains/disease states for clinical investigation.

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Two completed Phase II double-blind trials related to Crohn’s disease and colitis in two different treatment platforms.

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Currently recruiting accruing patients for two additional Phase II trials.

•

By early 2019, TOP anticipates that three additional Phase II trials will have commenced.

Established companies may have a competitive advantage due to their size and experiences, positive cash flows and institutional networks. Many of TOP’s competitors may have significantly greater financial, technical and human resources than TOP do. Due to these factors, TOP’s competitors may have a range of competitive advantages and may obtain regulatory approval of their drug candidates before TOP is able to develop or commercialize any drug candidates. TOP’s competitors may also develop drugs that are safer, more effective, more widely used and less expensive than those of TOP. Furthermore, some of these competitors may make acquisitions or establish collaborative relationships among themselves or with third parties to increase their ability to rapidly gain market share and/or increase their drug line. Large pharmaceutical companies may eventually enter or dominate the market for cannabinoid-derived pharmaceutical products. Given the rapid changes affecting the global, national, and regional economies in general and cannabis-related medical research and development in particular, TOP may not be able to create and maintain a competitive advantage in the marketplace. Time-to-market is an important factor and TOP’s success will depend on TOP’s ability to identify and develop innovative products that will be accepted by patients, regulators and insurance carriers.

TOP’s drug candidates may compete with synthetic and/or plant-derived cannabinoid drugs, in addition to competing with medical and recreational cannabis, in states or countries where the recreational and/or medical use of cannabis is legal. There is support in the United States for further legalization of cannabis, and as a result in markets where recreational and/or medical cannabis is not legal, TOP’s drug candidates may compete with cannabis purchased in the state-illegal drug market.

Mergers and acquisitions in the pharmaceutical and biotechnology industries may result in even more resources being concentrated among a smaller number of competitors. Smaller and other early-stage companies, such as TOP, may also prove to be significant competitors, particularly through collaborative arrangements with large and established companies. TOP anticipates competition in the United States with large and small companies in recruiting and retaining qualified scientific, management and commercial personnel, establishing clinical trial sites and subject registration for clinical trials, as well as in acquiring technologies complementary to its research projects.

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Government Laws and Regulations

TOP is an early stage company that ultimately intends to have its drug candidates approved in the U.S. If TOP commences this approval process, it would be subject to extensive regulation by regulatory agencies and its research and development, future manufacturing, distribution and sale of its drugs will become subject to the United States’ federal Controlled Substances Act of 1970 and regulations promulgated thereunder. While cannabis (other than Exempt Hemp Products) is a Schedule I controlled substance, drugs approved for medical use in the United States that contain cannabis or cannabis extracts must be placed in Schedules II-V, since approval by the FDA satisfies the “accepted medical use” requirement. Depending on the schedule onto which TOP’s approved drug candidates, if any, are placed, the manufacture, importation, exportation, domestic distribution, storage, sale and legitimate use of TOP’s future drugs may be subject to a significant degree of regulation by the DEA. In addition, individual states in the United States have also established controlled substance laws and regulations. Though state-controlled substances laws often mirror federal law, because the states are separate jurisdictions, they may ultimately be more restrictive than the CSA.

The U.S. Food, Drug, and Cosmetic Act (the “FDCA”) and its implementing regulations set forth, among other things, requirements for the research, testing, development, manufacture, quality control, safety, effectiveness, approval, labeling, storage, record keeping, reporting, distribution, import, export, advertising and promotion of drugs. Generally, TOP’s activities in other countries are and/or will be subject to regulations that are similar in nature and scope as those in the United States, although there can be important differences. Additionally, some significant aspects of regulation in the European Union are addressed in a centralized way through the EMA and the European Commission, but country-specific regulation remains essential in many respects. The process of obtaining regulatory marketing approvals and the subsequent compliance with appropriate federal, state, local and foreign statutes and regulations require the expenditure of substantial time and financial resources, and TOP may not be successful.

Regulations Related to the Drug Approval Process

TOP operates in a highly controlled regulatory environment. Strict regulations establish requirements relating to analytical, toxicological and clinical standards and protocols with respect to the testing of pharmaceuticals. Regulations also cover research, development, manufacturing and reporting procedures, sales and marketing, and advertising and promotional efforts, both pre- and post-approval. Failure to comply with regulations can result in stringent sanctions, including product recalls, withdrawal of approvals, seizure of products, civil penalties, and criminal prosecution. Further, many countries have stringent regulations relating to the possession and use of cannabis and/or drugs derived from cannabis.

Before obtaining regulatory approvals for the commercial sale of future drug candidates, TOP must demonstrate through pre-clinical studies and clinical trials that its drug candidates are safe and effective. Historically, the results from pre-clinical studies and early clinical trials often have not accurately predicted results of later clinical trials. In addition, many therapeutic candidates have shown promising results in clinical trials but subsequently failed to establish sufficient safety and efficacy results to obtain necessary regulatory approvals.

TOP has incurred and expects to incur substantial expense for, and continue to devote a significant amount of time to, pre-clinical studies and clinical trials. Many factors can delay the commencement and rate of completion of clinical trials, including the inability to recruit patients at the expected rate, the inability to follow patients adequately after treatment, the failure to manufacture sufficient quantities of materials used for clinical trials, or the emergence of unforeseen safety issues and governmental and regulatory delays. If a drug candidate fails to demonstrate safety and efficacy in clinical trials, this failure may delay development of other drug candidates, prevent receipt of regulatory clearance or approval and, ultimately, the commercialization of these products, and hinder TOP’s ability to conduct related pre-clinical studies and clinical trials in general. Additionally, if TOP experiences such failures, it may also experience challenges, delays or even the inability to obtain additional financing on acceptable terms and conditions.

Governmental authorities in all major markets require that a new drug be approved or exempted from approval before it is marketed, and have established high-standards for technical appraisal, which can result in an expensive and lengthy approval process. The time to obtain approval varies by country and some drugs are never approved. The lengthy process of conducting clinical trials, seeking approval and the

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subsequent compliance with applicable statutes and regulations, if approval is obtained, are very costly and require the expenditure of substantial resources.

United States

TOP intends to conduct some of its research and development relating to its drug candidates in the United States, at which time, TOP’s research and development, future manufacturing, distribution and sale of TOP’s drugs will become subject to the United States’ federal Controlled Substances Act of 1970 and regulations promulgated thereunder, which, among other things, places controlled substances onto one of five schedules, ranging from most restrictive to least. Cannabis (other than Exempt Hemp Products) is currently classified under Schedule I, which is reserved for those drug products viewed as having a high potential for abuse with no currently accepted medical use in treatment in the United States. No prescriptions may be written for Schedule I substances, and such substances are subject to production quotas imposed by the U.S. Drug Enforcement Administration (DEA). Accordingly, drugs approved for medical use in the United States that contain cannabis or cannabis extracts must be placed in Schedules II-V, since approval by the FDA satisfies the “accepted medical use” requirement. Depending on the schedule onto which TOP’s approved drug candidates, if any, are placed, the manufacture, importation, exportation, domestic distribution, storage, sale and legitimate use of TOP’s future drugs may be subject to a significant degree of regulation by the DEA. In addition, individual states in the United States have also established controlled substance laws and regulations. Though state-controlled substances laws often mirror federal law, because the states are separate jurisdictions, they may ultimately be more restrictive than the CSA.

Pre-clinical tests include in vitro and in vivo evaluation of the drug candidate, its chemistry, formulation and stability, and animal studies to assess potential safety and efficacy. Pre-clinical tests must be conducted in compliance with good laboratory practice regulations. Violations of these regulations can, in some cases, lead to invalidation of the studies, requiring them to be replicated. After laboratory analysis and pre-clinical testing, a sponsor files an Investigational New Drug Application, or IND, to begin human testing. Typically, a manufacturer conducts a three-phase human clinical testing program which itself is subject to numerous laws and regulatory requirements, including adequate monitoring, reporting, record keeping and informed consent. In Phase I, small clinical trials are conducted to assess endpoints, such as metabolism, pharmacokinetics, pharmacological actions, side effects associated with increasing doses, and, if possible, early evidence of effectiveness. Phase II clinical trials usually involve a limited patient population and are conducted to assess the effectiveness of the drug for a particular tissue-specific, or possibly genetically specific patient population, dosage tolerance, and optimum dosage, and to identify common adverse effects and safety risks. If a candidate demonstrates evidence of effectiveness and an acceptable safety profile in Phase II, Phase III clinical trials are conducted to obtain additional information about clinical efficacy and safety in a larger sample of patients, typically at geographically dispersed study sites, to provide the FDA with data to evaluate the overall risk-benefit relationship of the drug and information that may inform required labeling. The time and expense that will be required for TOP to perform this clinical testing can vary and is substantial. TOP cannot be certain that it will successfully complete Phase I, Phase II or Phase III testing for any drug candidate within any specific period, if at all. Furthermore, the FDA, applicable IRB(s), Data Safety Monitoring Board(s), where used or required, or TOP may suspend clinical trials for a given drug candidate at any time on various grounds, including finding that subjects or patients are exposed to unacceptable health risk.

If the clinical data from clinical trials (Phases I, II and III) are deemed to support the safety and effectiveness of any of TOP’s drug candidates for its intended use, then TOP may file with the FDA, a New Drug Application, or NDA, seeking approval to market the drug candidate for one or more specified intended uses. The purpose of the NDA is to provide the FDA with sufficient information so that it can assess whether it should approve the drug candidate for marketing for specific intended uses. The NDA normally contains, among other things, sections describing the chemistry, manufacturing, and controls, non-clinical pharmacology and toxicology, human pharmacokinetics and bioavailability, microbiology, the results of the clinical trials, and the proposed labeling which contains, among other things, the intended uses of the candidate drug. TOP has not completed clinical trials for any candidate drug for any intended use

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and therefore, cannot ascertain whether the clinical data will support and justify filing an NDA. Nevertheless, if and when TOP is able to ascertain that the clinical data supports and justifies filing an NDA, TOP intends to make such appropriate filing.

TOP cannot take any action to market any new drug in the United States until a marketing application has been approved by the FDA. The FDA has substantial discretion over the approval process and may disagree with TOP’s interpretation of the data submitted. The FDA has 60 days from its receipt of an NDA to determine whether the application will be accepted for filing based on a threshold determination that the application is sufficiently complete to permit a substantive review. Once a submission is accepted for filing, the FDA begins an exhaustive review, which currently takes ten-to-twelve months (but which may take a longer or shorter amount of time at the time (if ever) that TOP may be able to submit an NDA). The process may be significantly extended by requests for additional information or clarification regarding information already provided. As part of this review, the FDA may refer the application to an appropriate advisory committee, typically a panel of clinicians. Accordingly, the actual time required may vary substantially based upon the type, complexity and novelty of the drug. Government regulation may delay or prevent marketing of potential drugs for a considerable period and impose costly procedures on TOP’s activities. TOP cannot be certain that the FDA or other regulatory agencies will approve any of its proposed drugs in a timely manner, if at all. Success in pre-clinical or early stage clinical trials does not assure success in later-stage clinical trials. Even if a drug receives regulatory approval, the approval may be significantly limited to specific indications or uses and these limitations may adversely affect the commercial viability of the drug. Delays in obtaining, or failure to obtain, regulatory approvals, would have a material adverse effect on the business of TOP.

Even after TOP obtains FDA approval, it will be subject to pervasive and continuing regulation by the FDA and other regulatory agencies. Such post-approval regulatory requirements include, without limitation, recordkeeping requirements; adverse event reporting; providing updated safety and efficacy information via postmarket clinical trials (i.e., Phase IV trials); therapeutic sampling and distribution requirements; and complying with FDA promotion and advertising requirements, which include, among other things, standards for direct-to-consumer advertising, restrictions on promoting products for uses or in patient populations not consistent with the product’s approved labeling, limitations on industry-sponsored scientific and educational activities, and requirements for promotional activities involving the Internet. TOP also would be required to gain separate approval for the use or promotion of an approved drug as a treatment for indications other than those initially approved. In addition, side effects or adverse events that are reported during clinical trials can delay, impede or prevent marketing approval. Similarly, adverse events that are reported after marketing approval can result in additional limitations being placed on the drug’s use and, potentially, withdrawal of the drug from the market. Any adverse event, either before or after marketing approval, can result in product liability claims against TOP.

Additionally, therapeutic manufacturers, their subcontractors, and other entities involved in the manufacture and distribution of approved therapeutic candidates are required to register their establishments with the FDA and certain state agencies and are subject to periodic unannounced inspections by the FDA and some state agencies for compliance with current Good Manufacturing Practices (cGMPs). The FDA periodically inspects manufacturing facilities to assess compliance with ongoing regulatory requirements, including cGMPs, which impose extensive procedural, substantive, and record-keeping requirements upon TOP and any third-party manufacturers that it may decide to use if its drug products are approved. In addition, changes to the manufacturing process are strictly regulated, and, depending on the significance of the change, may require FDA approval before being implemented. FDA regulations would also require investigation and correction of any deviations from cGMPs and impose reporting and documentation requirements upon TOP and the third-party manufacturers, if any. Accordingly, manufacturers must continue to expend time, money and effort in the area of production and quality control to maintain compliance with cGMPs and other aspects of regulatory compliance. Failure to comply with the statutory and regulatory requirements may give rise to possible legal or regulatory actions, including, without limitation, warning letters, product recalls, seizure, injunction, and civil penalties.

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Orphan Drug Designation in the U.S.

Under the Orphan Drug Act, the FDA may grant orphan drug designation to a drug intended to treat a rare disease or condition, which is a disease or condition that affects fewer than 200,000 individuals in the United States. If the disease or condition affects more than 200,000 individuals in the United States, orphan drug designation may nevertheless be available if there is no reasonable expectation that the cost of developing and making the drug would be recovered from sales in the United States. In the United States, a drug that has received orphan drug designation is eligible for financial incentives, such as opportunities for grant funding towards clinical trial costs, tax credits for certain research and user fee waivers under certain circumstances. The Orphan Drug Act provides that, if a designated drug is approved for the rare disease or condition for which it was designated, the approved drug will be granted seven years of orphan drug exclusivity, which means the FDA generally will not approve any other application for a drug containing the same active moiety for the same indication for a period of seven years, except in limited circumstances, such as a showing of clinical superiority over the drug with orphan drug exclusivity. Orphan drug exclusivity does not prevent the FDA from approving a different drug for the same disease or condition, or the same drug for a different disease or condition. In the European Union, orphan drug designation also entitles a party to financial incentives such as a reduction of fees or fee waivers and ten years of market exclusivity following drug approval. This period may be reduced to six years if the orphan drug designation criteria are no longer met, including where it is shown that the drug is sufficiently profitable not to justify maintenance of market exclusivity.

Orphan drug designation must be requested before submission of an application for marketing approval. Products that qualify for orphan designation may also qualify for other FDA programs that are intended to expedite the development and approval process and, as a practical matter, clinical trials for orphan products may be smaller, simply because of the smaller patient population. Nonetheless, the same approval standards apply to orphan-designated products as for other drugs. Orphan drug designation does not convey any advantage in, or shorten the duration of, the regulatory review and approval process.

Priority Review, Fast Track, Breakthrough Therapy, and Accelerated Approval

The FDA has programs to expedite submission and consideration of certain drug drugs that address serious or life-threatening diseases or conditions. An application for a drug will receive priority review designation if it is for a drug that treats a serious condition and, if approved, would provide a significant improvement in safety or effectiveness. Priority review means that FDA will seek to complete its first-cycle review and take action on the application within six months rather than the customary ten-month standard review period. An applicant may request priority review at the time it submits its application. Priority review designation does not change the scientific/medical standard for approval or the quality of evidence necessary to support approval.

Additionally, the fast track program is intended to expedite or facilitate the process for reviewing new drugs that demonstrate the potential to address unmet medical needs involving serious or life-threatening diseases or conditions. If a drug receives fast track designation, the FDA may consider reviewing sections of the NDA on a rolling basis, rather than requiring the entire application to be submitted to begin the review. Products with fast track designation also may be eligible for more frequent meetings and correspondence with the FDA about the drug’s development. Other FDA programs intended to expedite development and review include accelerated approval (approval based on a surrogate endpoint that is reasonably likely to predict clinical benefit) and breakthrough therapy designation, which is available for drugs under development for serious or life-threatening conditions and where preliminary clinical evidence shows that the drug may have substantial improvement on at least one clinically significant endpoint over available therapy. If a drug receives breakthrough therapy designation, it will be eligible for the benefits of fast track designation, as well as for more intensive guidance from the FDA on an efficient drug development program and a commitment from the agency to involve senior FDA managers in such guidance. Even if a drug qualifies for fast track designation or breakthrough therapy designation, the FDA may later decide that the drug no longer meets the conditions for these designations, and/or may determine that the drug does not meet the standards for approval.

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In addition to regulating and auditing human clinical trials, the FDA regulates and inspects equipment, facilities, laboratories and processes used in the manufacturing and testing of drugs prior to providing approval to market a drug.

Pediatrics

Under the Pediatric Research Equity Act (PREA), NDAs or supplements to NDAs must contain data to assess the safety and efficacy of the drug for the claimed indications in all relevant pediatric subpopulations and to support dosing and administration for each pediatric subpopulation for which the drug is safe and effective. The FDA may grant full or partial waivers, or deferrals, for submission of data. Unless otherwise required by regulation, PREA generally does not apply to a drug for an indication for which orphan designation has been granted; however, beginning in 2020, PREA will apply to NDAs for orphan-designated drugs if the drug is a molecularly targeted cancer product intended for the treatment of an adult cancer and is directed at a molecular target that FDA has determined is substantially relevant to the growth or progression of a pediatric cancer. The Best Pharmaceuticals for Children Act (BPCA) provides NDA holders a six-month extension of any exclusivity — patent or non-patent — for a drug if certain conditions are met. Conditions for exclusivity include the FDA’s determination that information relating to the use of a new drug in the pediatric population may produce health benefits in that population, FDA making a written request for pediatric studies, and the applicant agreeing to perform, and reporting on, the requested studies within the statutory timeframe. Applications under the BPCA are treated as priority applications with all of the benefits conferred by such designation.

Federal and State Healthcare Fraud and Abuse Laws and Regulations

If TOP obtains regulatory approval for its drug products, it may also be subject to various federal, state and international laws pertaining to health care “fraud and abuse,” among others. These laws include, without limitation, anti-kickback, false claims, and drug pricing and transparency laws and regulations.

The federal Anti-Kickback Statute makes it illegal to solicit, offer, receive or pay any remuneration in exchange for, or to induce, the referral of any healthcare item or service payable under federal healthcare programs (e.g., Medicare, Medicaid, etc.), including the purchase or prescription of a specific drug. Many states have similar laws that are not restricted to federal healthcare programs. Federal and state false claims laws prohibit anyone from knowingly and willingly presenting, or causing to be presented for payment to the federal government (including, but not limited to, Medicare and Medicaid), claims for reimbursement, including claims for the sale of drugs or services, that are false or fraudulent, claims for items or services not provided as claimed, or claims for medically unnecessary items or services.

The U.S. federal Health Insurance Portability and Accountability Act of 1996, or HIPAA, includes a fraud and abuse provision that imposes criminal and civil liability for executing a scheme to defraud any healthcare benefit program, or knowingly and willfully falsifying, concealing or covering up a material fact or making any materially false statement in connection with the delivery of or payment for healthcare benefits, items or services.

TOP may also be subject to federal transparency laws, including the federal Physician Payment Sunshine Act, which requires applicable manufacturers of drugs and biologics, among others, to track and disclose payments and other transfers of value they make to physicians and teaching hospitals, as well as physician ownership and investment interests in the manufacturer. This information is subsequently made publicly available in a searchable format online. Failure to disclose required information may result in substantial civil monetary penalties for all payments, transfers of value or ownership or investment interests that are not timely, accurately and completely reported in an annual submission. In addition, there has been a recent trend of increased federal and state regulation of payments made to physicians for marketing, medical directorships, and other purposes. Some states impose a legal obligation on companies to adhere to voluntary industry codes of behavior (e.g., the PhRMA Code and the AdvaMed Code of Ethics), which apply to pharmaceutical and medical device companies’ interactions with healthcare providers; some mandate implementation of corporate compliance programs, along with the tracking and reporting of gifts, compensation and other remuneration to physicians, and some states limit or prohibit such gifts.

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costs for drug products. Several states have passed or introduced bills that would require disclosure of certain pricing information for prescription drugs that have no threshold amount or are above a certain annual wholesale acquisition cost. For example, Vermont passed legislation requiring certain drug companies to disclose information relating to justification of certain price increases. The U.S. Congress has also introduced bills targeting prescription drug price transparency, and two such bills — the Patient Right to Know Drug Prices Act (for private plans) and the Know the Lowest Price Act (for Medicare Parts C and D) — were signed into law on October 10, 2018.

If the government or a private “whistleblower” were to allege that TOP violated these laws, there could be a material adverse effect on TOP and its business, including its stock price. Even an unsuccessful challenge could cause adverse publicity and be costly to respond to, which could have a material adverse effect on TOP’s business, results of operations and financial condition. A finding of liability under these laws can have significant adverse financial implications for TOP and can result in payment of large penalties and possible exclusion from federal healthcare programs. Given the complexity and broad reach of these laws and regulations, and the increasing attention given by law enforcement authorities, TOP cannot assure you that some of its activities, or the activities of its employees, partners, agents, or other affiliates, will not be challenged or deemed to violate some of these laws.

The Foreign Corrupt Practices Act

The Foreign Corrupt Practices Act (“FCPA”) prohibits any U.S. individual or business from paying, offering, or authorizing payment or offering of anything of value, directly or indirectly, to any foreign official, political party or candidate for the purpose of influencing any act or decision of the foreign entity in order to assist the individual or business in obtaining or retaining business. The FCPA also obligates companies whose securities are listed in the United States to comply with accounting provisions requiring such companies to maintain books and records that accurately and fairly reflect all transactions of the corporation, including international subsidiaries, and to devise and maintain an adequate system of internal accounting controls for international operations.

European and Other International Government Regulation

In addition to regulations in the United States, TOP will be subject to a variety of regulations in other jurisdictions governing, among other things, clinical trials and any commercial sales and distribution of TOP’s drugs. Regardless of whether TOP obtains FDA approval for a drug, TOP must obtain the requisite approvals from regulatory authorities in foreign countries prior to the commencement of clinical trials or marketing of the drug in those countries.

Approximately 250 substances, including cannabis, are listed in the Schedules annexed to the United Nations Single Convention on Narcotic Drugs (New York, 1961, amended 1972), the Convention on Psychotropic Substances (Vienna, 1971) and the Convention against Illicit Traffic in Narcotic Drugs and Psychotropic Substances (introducing control on precursors) (Vienna, 1988). The purpose of these listings is to control and limit the use of these drugs according to a classification of their therapeutic value, risk of abuse and health dangers, and to minimize the diversion of precursor chemicals to illegal drug manufacturers. The 1961 UN Single Convention on Narcotic Drugs, as amended in 1972 classifies cannabis as Schedule I (“substances with addictive properties, presenting a serious risk of abuse”) and as Schedule IV (“the most dangerous substances, already listed in Schedule I, which are particularly harmful and of extremely limited medical or therapeutic value”) narcotic drug. The 1971 UN Convention on Psychotropic Substances classifies THC — the principal psychoactive cannabinoid of cannabis — as a schedule I psychotropic substance (Substances presenting a high-risk of abuse, posing a particularly serious threat to public health which are of very little or no therapeutic value).

Most countries in Europe are parties to these conventions which govern international trade and domestic control of these substances, including cannabis. They may interpret and implement their obligations in a way that creates a legal obstacle to TOP obtaining manufacturing and/or marketing approval for its drugs in those countries. These countries may not be willing or able to amend or otherwise modify their laws and regulations to permit TOP’s drug candidates to be manufactured and/or marketed, or achieving such amendments to the laws and regulations may take a prolonged period.

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Some countries outside of the United States have a similar process that requires the submission of a clinical trial application (“CTA”), much like the submissions of an IND in the U.S. prior to the commencement of human clinical trials. In the European Union, for example, a CTA must be submitted to the national health authority of each EU Member State in which the clinical trial is to be conducted and an independent ethics committee, much like the FDA and IRB, respectively. Once the CTA is approved in accordance with a country’s requirements, clinical trial development may proceed.

To obtain regulatory approval to commercialize a new drug under regulatory systems in the European Union, TOP must submit a marketing authorization application, or MAA. In the European Union, marketing authorization for a drug can be obtained through a centralized, mutual recognition, decentralized procedure, or the national procedure of an individual EU Member State. In accordance with the centralized procedure, the applicant may submit a single application for marketing authorization to the EMA. The agency will provide a positive opinion regarding the application if it meets certain quality, safety, and efficacy requirements. Following the opinion of the EMA, the European Commission makes a final decision to grant a centralized marketing authorization that permits the marketing of a drug in all 28 EU Member States and three of the four European Free Trade Associations (“EFTA”) states: Iceland, Liechtenstein and Norway. The centralized procedure is mandatory for certain medicinal drugs, including orphan drugs, drugs derived from certain biotechnological processes, advanced therapy drugs and certain other drugs containing a new active substance for the treatment of certain diseases. This route is optional for certain other drugs, including drugs that are a significant therapeutic, scientific or technical innovation, or whose authorization would be in the interest of public or animal health.

Unlike the centralized authorization procedure, the decentralized marketing authorization procedure requires a separate application to, and leads to separate approval by, the competent authorities of each EU Member State in which the drug is to be marketed. This application process is identical to the application that would be submitted to the EMA for authorization through the centralized procedure. The applicable EU Member State prepares a draft assessment and drafts of the related materials within 120 days after receipt of a valid application. The resulting assessment report is submitted to the concerned EU Member States who, within 90 days of receipt, must decide whether to approve the assessment report and related materials. If a EU Member State cannot approve the assessment report and related materials due to concerns relating to a potential serious risk to public health, disputed elements may be referred to the European Commission, whose decision is binding on all EU Member States.

The mutual recognition procedure is similarly based on the acceptance by the competent authorities of the EU Member States of the marketing authorization of a drug by the competent authorities of other EU Member States. The holder of a national marketing authorization may submit an application to the competent authority of another EU Member State requesting that this authority recognize the marketing authorization delivered by the competent authority of the other EU Member State.

For countries outside of the European Union, including countries in Eastern Europe, Latin America or Asia, the requirements governing the conduct of clinical trials, drug licensing, pricing and reimbursement vary from country to country. Internationally, clinical trials are generally required to be conducted in accordance with GCP, applicable regulatory requirements of each jurisdiction and the medical ethics principles that have their origin in the Declaration of Helsinki.

In the European Union, if a marketing authorization is granted for a drug containing a new active substance, that drug benefits from eight years of data exclusivity, during which generic marketing authorization applications referring to the data of that drug may not be accepted by the regulatory authorities, and a further two years of market exclusivity, during which such generic drugs may not be placed on the market. The two-year period may be extended to three years if during the first eight years a new therapeutic indication with significant clinical benefit over existing therapies is approved.

Orphan Drug Designation in the European Union

In the European Union, the EMA’s Committee for Orphan Medicinal Products grants orphan drug designation to promote the development of drugs that are intended for the diagnosis, prevention or treatment of life-threatening or chronically debilitating conditions affecting not more than five in 10,000 persons in the European Union. Additionally, orphan drug designation is granted for drugs intended for the

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diagnosis, prevention or treatment of a life-threatening, seriously debilitating or serious and chronic condition and when, without incentives, it is unlikely that sales of the drug in the European Union would be sufficient to justify the necessary investment in developing the drug. The application for orphan designation must be submitted to the EMA and approved before an application is made for marketing authorization for the drug. Once authorized, orphan drugs are entitled to ten years of market exclusivity. During this ten-year period, with a limited number of exceptions, neither the competent authorities of the EU Member States, the EMA, or the European Commission are permitted to accept applications or grant marketing authorization for other similar drugs with the same therapeutic indication. However, marketing authorization may be granted to a similar medicinal drug with the same orphan indication during the ten-year period with the consent of the marketing authorization holder for the original orphan medicinal drug or if the manufacturer of the original orphan medicinal drug is unable to supply sufficient quantities. Marketing authorization may also be granted to a similar drug with the same orphan indication if this latter drug is safer, more effective or otherwise clinically superior to the original orphan drug. The period of market exclusivity may, in addition, be reduced to six years if it can be demonstrated based on available evidence that the original orphan medicinal drug is sufficiently profitable not to justify maintenance of market exclusivity.

Accelerated Review

Under the Centralized Procedure in the European Union, the maximum timeframe for the evaluation of a MAA is 210 days (excluding “clock stops,” when additional written or oral information is to be provided by the applicant in response to questions asked by the Committee for Medicinal Products for Human Use, or CHMP). Accelerated evaluation might be granted by the CHMP in exceptional cases, when a medicinal drug is expected to be of a major public health interest. Three cumulative criteria must be fulfilled in such circumstances: the seriousness of the disease (e.g., heavy disabling or life-threatening diseases) to be treated; the absence or insufficiency of an appropriate alternative therapeutic approach; and anticipation of high therapeutic benefit. In this circumstance, EMA ensures that the opinion of the CHMP is given within 150 days.

Well-Established Medicinal Use

Under Article 10a of Directive 2001/83/EC, an applicant may, in substitution for the results of its own preclinical and clinical research, present detailed references to published literature demonstrating that the active substance(s) of a drug have a well-established medicinal use within the community with recognized efficacy and an acceptable level of safety. The applicant is entitled to refer to a variety of different types of literature, including reports of clinical trials with the same active substance(s) and epidemiological studies that indicate that the constituent or constituents of the drug have an acceptable safety/efficacy profile for a particular indication. However, use of the published literature exemption is restricted because in no circumstances will constituents be treated as having a well-established use if they have been used for less than 10 years from the first systematic and documented use of the substance as a medicinal drug in the EU. Even after 10 years of systematic use, the threshold for well-established medicinal use might not be met. European pharmaceutical law requires the competent authorities to consider among other factors, the period over which a substance has been used, the amount of patient use of the substance, the degree of scientific interest in the use of the substance (as reflected in the scientific literature) and the coherence (consistency) of all the scientific assessments made in the literature. For this reason, different substances may reach the threshold for well-established use after different periods, but the minimum period is 10 years. If the applicant seeks approval of an entirely new therapeutic use compared with that to which the published literature refers, additional pre-clinical and/or clinical results are required.

Informed Consent

Under Article 10c of Directive 2001/83/EC, following the grant of a marketing authorization the holder of such authorization may consent to a competent authority utilizing the pharmaceutical, preclinical and clinical documentation that it submitted to obtain approval for a medicinal drug to assess a subsequent application relating to a medicinal drug possessing the same qualitative and quantitative composition with respect to the active substances and the same pharmaceutical form.

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Law Relating to Pediatric Research

Regulation (EC) 1901/2006 (as amended by Regulation (EC) 1902/2006) governs the development of medicinal drugs for human use to meet the specific therapeutic needs of the pediatric population. It requires any application for marketing authorization made after July 26, 2008 in respect of a drug not authorized in the European Community on January 26, 2007 (the time the regulation entered into force), to include the results of all studies performed and details of all information collected in compliance with a pediatric investigation plan agreed by the Pediatric Committee of the EMA, unless the drug is subject to an agreed waiver or deferral or unless the drug is excluded from the scope of Regulation 1902/2006 (generics, hybrid medicinal drugs, biosimilars, homeopathic and traditional (herbal) medicinal drugs and medicinal drugs containing one or more active substances of well-established medicinal use). Waivers can be granted in certain circumstances where pediatric studies are not required or desirable. Deferrals can be granted in certain circumstances where the initiation or completion of pediatric studies should be deferred until appropriate studies in adults have been performed. Moreover, this regulation imposes the same obligation from January 26, 2009 on an applicant seeking approval of a new indication, pharmaceutical form or route of administration for a drug already authorized and still protected by a supplementary protection certificate granted under Regulation EC 469/2009 and its predecessor (EEC) 1768/92 or by a patent that qualifies for the granting of such a supplementary protection certificate. The pediatric Regulation 1901/2006 also provides, subject to certain conditions, a reward for performing such pediatric studies, regardless of whether the pediatric results provided resulted in the grant of a pediatric indication. This reward comes in the form of an extension of six months to the supplementary protection certificate granted in respect of the drug, unless the drug is subject to orphan drug designation, in which case the 10-year market exclusivity period for such orphan drugs is extended to 12 years. If any of the non-centralized procedures for marketing authorization have been used, the six-month extension of the supplementary protection certificate is only granted if the medicinal drug is authorized in all member states.

Post-Authorization Obligations

In the pre-authorization phase, the applicant must provide a detailed pharmacovigilance plan that it intends to implement post-authorization. An authorization to market a medicinal drug in the EU carries with it an obligation to comply with many post-authorization organizational and behavioral regulations relating to the marketing and other activities of authorization holders. These include requirements relating to post-authorization efficacy studies, post-authorization safety studies, adverse event reporting and other pharmacovigilance requirements, advertising, packaging and labeling, patient package leaflets, distribution and wholesale dealing. The regulations frequently operate within a criminal law framework and failure to comply with the requirements may not only affect the authorization, but also can lead to financial and other sanctions levied on the company in question and responsible officers. Because of the currently on-going overhaul of EU pharmacovigilance legislation, the financial and organizational burden on market authorization holders will increase significantly, including pursuant to the obligation to maintain a pharmacovigilance system master file that applies to all holders of marketing authorizations granted in accordance with Directive 2001/83/EC or Regulation (EC) No 726/2004. Marketing authorization holders must also collect data on adverse events associated with use of the authorized drug outside the scope of the authorization. Pharmacovigilance for biological drugs and medicines with a new active substance will be strengthened by subjecting their authorization to additional monitoring activities. The EU is currently in the process of issuing implementing regulations for the new pharmacovigilance framework.

Any authorization granted by member state authorities, which within three years of its granting is not followed by the actual placing on the market of the authorized drug in the authorizing member state, ceases to be valid. When an authorized drug previously placed on the market in the authorizing member state is no longer actually present on the market for a period of three consecutive years, the authorization for that drug shall cease to be valid. The same two three-year periods apply to authorizations granted by the European Commission based on the centralized procedure.

Israel

TOP, with the cooperation of TOL, has been conducting in Israel pre-clinical trials and randomized, placebo-controlled clinical trials using cannabinoid-based compounds to develop unique, condition-specific formulas based on TOL products. To conduct clinical testing on humans in Israel, special authorization

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must first be obtained from the ethics committee and general manager of the institution where the clinical studies are scheduled to be conducted, as required under the Guidelines for Clinical Trials in Human Subjects implemented pursuant to the Israeli Public Health Regulations (Clinical Trials in Human Subjects), as amended from time to time, and other applicable legislation. These regulations also require authorization from the Israeli Ministry of Health, except in certain circumstances, and in the case of genetic trials, special fertility trials and similar trials, an additional authorization of the overseeing institutional ethics committee. The institutional ethics committee must, among other things, evaluate the anticipated benefits that are likely to be derived from the project to determine if it justifies the risks and inconvenience to be inflicted on the human subjects, and the committee must ensure that adequate protection exists for the rights and safety of the participants as well as the accuracy of the information gathered from the clinical testing.

Israel’s Ministry of Health (“Ministry of Health”), which regulates medical testing, has adopted protocols that correspond, generally, to those of the FDA and the EMA, making it comparatively straightforward for studies conducted in Israel to satisfy FDA and the EMA’s requirements, thereby enabling medical technologies subjected to clinical trials in Israel to reach U.S. and EU commercial markets in an expedited fashion. Many members of Israel’s medical community have earned international prestige in their chosen fields of expertise and routinely collaborate, teach and lecture at leading medical centers throughout the world. Israel also has free trade agreements with the United States and the European Union.

The cannabinoid-based drugs TOP intends to develop contain a controlled substance (cannabis) as defined in the Israeli Dangerous Drugs Ordinance [New Version], 5733 – 1973. The research facilities through which TOP and TOL conduct research are located, at present, in Israel, where licenses to cultivate, possess and supply cannabis for medical research are granted by the Ministry of Health on an ad-hoc basis. TOP has initially used TOL’s research facilities but has not yet determined where any of its own research facilities, if any, may be located. TOP requires that the research facilities with which it enters into collaborative agreements maintain their existing licenses to conduct medical-based cannabinoid research. TOP may be required to obtain additional licenses and permits related to medical research for other prospect products if TOP enters into collaboration agreements with other hospitals or research institutes, which may include authorization from the ethics committee and general manager of each institution in which TOP intends to conduct its clinical trials, and in most cases, from the Ministry of Health.

Research and Development Activities

TOP incurred expenses of $235,096 and $106,179 during the fiscal years ended December 31, 2017 and 2016, respectively, and $340,109 and $73,822 for the nine-month periods ended September 30, 2018 and 2017, respectively, on research and development. None of these research or development costs are borne by any customers.

Employees

We currently have two employees engaged in executive management, including supervising third parties conducting drug candidate development, as well as relationships with third-party firms and individuals. We have one consultant who serves as our interim chief medical officer. Our employees are not subject to any collective bargaining agreement.

DESCRIPTION OF PROPERTY

TOP’s principal office is located at 77 Water Street, 8th Floor, New York, New York 10005. TOP’s telephone number is (303) 495-7583. TOP’s offices consist of approximately 200 square feet of executive offices and TOP believes that these facilities will be sufficient for the next twelve months.

LEGAL PROCEEDINGS

There are no pending legal proceedings to which TOP is a party, and TOP’s property is not the subject of any pending legal proceedings.

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MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS OF AQUAMED

The following discussion and analysis is intended to help prospective investors understand our business, financial condition, results of operations, liquidity and capital resources. You should read this discussion in conjunction with our combined financial statements and related notes thereto included elsewhere in this prospectus.

The statements in this discussion regarding industry outlook, expectations regarding our future performance, liquidity and capital resources and other non-historical statements are forward-looking statements. These forward-looking statements are subject to numerous risks and uncertainties, including, but not limited to, the risks and uncertainties described in “Risk Factors” and “Special Note Regarding Forward-Looking Statements.” Actual results may differ materially from those contained in any forward-looking statements.

The AquaMed Financial Statements and unaudited Interim Condensed Financial Statements, discussed below, reflect the AquaMed financial condition, results of operations, and cash flows. The financial information discussed below and included in this prospectus, however, may not necessarily reflect what the AquaMed financial condition, results of operations, or cash flows would have been had AquaMed been operated as a separate, independent entity during the periods presented, or what the AquaMed financial condition, results of operations, and cash flows may be in the future.

Overview

We manufacture a high-water content, electron beam cross-linked, aqueous polymer hydrogels, or gels, used for wound care, medical diagnostics, transdermal drug delivery and cosmetics. We believe that we are one of the leading manufacturers of high-performance gels in the United States. We specialize in custom gels by capitalizing on proprietary manufacturing technologies. We have historically served as a contract manufacturer, supplying our gels to third parties who incorporate them into their own products. Our contract manufacturing business provides custom hydrogels to the OEM market.

Liquidity and Capital Resources

As of September 30, 2018, we had no cash and cash equivalents as we are a carve out of Alliqua’s contract manufacturing business, all cash management and other treasury-related functions on a centralized basis for all of its divisions, were performed by Alliqua.

Net cash used in operating activities was $1.2 million and $0.8 million for the nine months ended September 30, 2018 and 2017, respectively.

Net cash used in investing activities was nominal for the nine months ended September 30, 2018, and 2017, respectively.

Net cash used in financing activities for the nine months ended September 30, 2018 consisted of the advances from the Parent, Alliqua.

At September 30, 2018, current assets totaled $0.7 million and current liabilities totaled $0.6 million, as compared to current assets totaling $0.2 million and current liabilities totaling $0.2 million at December 31, 2017. As a result, we had working capital of $0.1 million at September 30, 2018 compared to working capital of $0 at December 31, 2017.

The Company expects to continue incurring losses for the foreseeable future and will need to raise additional capital to support ongoing operations.

Management is evaluating all options to raise sufficient funds to fund the Company’s working capital requirements through equity offerings. There can be no assurances, however, that management will be able to obtain sufficient additional funds when needed, or that such funds, if available, will be obtained on terms satisfactory to the Company. The ability of the Company to continue as a going concern is dependent upon its ability to raise additional capital and achieve profitable operations. The financial statements do not include any adjustments relating to the recoverability and classification of recorded assets and liabilities that might be necessary should the Company be unable to continue as a going concern.

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Results of Operations

Year Ended December 31, 2017 Compared to the Year Ended December 31, 2016

Revenues, net. For the year ended December 31, 2017 revenues decreased by $0.2 million, or 7%, to $1.9 million from $2.1 million for the year ended December 31, 2016. The decrease in our overall revenue was due to a decrease in orders from contract manufacturing customers.

Gross profit. Our gross profit was $0.147 million for the year ended December 31, 2017 compared to gross loss of ($0.114 million) for the year ended December 31, 2016. The improved results for the year ended December 31, 2017, as compared to the year ended December 31, 2016 was primarily due to a decrease in stock-based compensation and a stricter emphasis on manufacturing operating efficiency. Gross margin was approximately 7% for the year ended December 31, 2017. Gross margin was approximately a negative (5%) for the year ended December 31, 2016.

The components of cost of revenues are as follows for the years ended December 31, 2017 and 2016 (in thousands):

	Year Ended December 31,
	2017			2016
Cost of revenues
Materials and finished products		$	674		$	629
Stock-based compensation			45			184
Compensation and benefits			481			616
Depreciation and amortization			288			288
Equipment, production and other expenses			357			549
Total cost of revenues		$	1,845		$	2,266

Selling, general and administrative expenses. The following table highlights selling, general and administrative expenses by type for the years ended December 31, 2017 and 2016 (in thousands):

	Year Ended December 31,
	2017			2016
Selling, general and administrative expenses
Compensation and benefits		$	184		$	269
Stock-based compensation			198			563
Other expenses and professional fees			734			918
Total selling, general and administrative expenses		$	1,116		$	1,750

Selling, general and administrative expenses decreased by $0.7 million to $1.1 million for the year ended December 31, 2017, as compared to $1.8 million for the year ended December 31, 2016. The decrease in selling, general and administrative expenses is attributable to our organizational focus on managing operating expenditures and decrease in stock-based compensation.

Compensation and benefits decreased by $0.1 million to $0.2 million for the year ended December 31, 2017, as compared to $0.3 million for the year ended December 31, 2016. The decrease in compensation and benefits was primarily due to the decrease in the average number of full-time employees in 2017 compared to 2016.

Stock-based compensation decreased by $0.4 million, to $0.2 million for the year ended December 31, 2017, as compared to $0.6 million for the year ended December 31, 2016. The decrease in stock-based compensation is primarily due to a reduced amount of unvested employee stock options outstanding.

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Other expenses and professional fees decreased by $0.2 million to $0.7 million for the year ended December 31, 2017 from $0.9 million for the year ended December 31, 2016. Other selling, general and administrative expenses consist of costs associated with our selling efforts and general management, including information technology, travel, training and recruiting. The decrease is due to lower legal and consulting fees.

Income tax benefit. During the year ended December 31, 2017, we recorded an income tax benefit of approximately $16,000. The income tax benefit is primarily attributable to the impairment of goodwill assets. During the year ended December 31, 2016, we recorded an income tax benefit of approximately $64,000.

On December 22, 2017 the U.S. government enacted significant changes to federal tax law following the passage of the Tax Cuts and Jobs Act (“the Act”). The Act significantly changes the U.S. corporate tax system. The Company has reasonably estimated the accounting for the effects of the Act during the year ended December 31, 2017. Our financial statements for the year ended December 31, 2017 reflect certain effects of the Act including a reduction in the corporate tax rate from 34% to 21%. As we have recorded a full valuation allowance against our net deferred tax assets as of December 31, 2017, these changes have no impact on the income tax benefit for year ending December 31, 2017. Given the significant changes resulting from and complexities associated with the Act, the financial impacts for the fourth quarter and full year 2017 are provisional and subject to further analysis, interpretation and clarification of the Act, which could result in changes to these estimates during 2018. The Company will reflect any adjustments to the provisional amounts within one year from the enactment date of the Act, if applicable. For additional discussion of the impact on the income tax provision, other income tax balances and related disclosures, see “Note 9 — Income Taxes” in the Notes accompanying the audited Consolidated Financial Statements.

Nine Months Ended September 30, 2018 Compared to the Nine Months Ended September 30, 2017

Revenues, net. For the nine months ended September 30, 2018 revenues increased by $0.5 million, or 32%, to $1.8 million from $1.3 million for the nine months ended September 30, 2017. The increase in our overall revenue was due to an increase in orders fulfilled for our contract manufacturing customers.

Gross profit. Our gross profit was $0.4 million for the nine months ended September 30, 2018 compared to gross profit of $0.004 million for the nine months ended September 30, 2017. The improved results for the nine months ended September 30, 2018, as compared to the nine months ended September 30, 2017 was primarily due to the greater volume of contract manufacturing fulfilled orders and a stricter emphasis on operating efficiency. Gross margin was approximately 23% for the nine months ended September 30, 2018. Gross margin was approximately 1% for the nine months ended September 30, 2017.

The components of cost of revenues are as follows for the nine months ended September 30, 2018 and 2017 (in thousands):

	Nine Months Ended September 30,
	2018			2017
Cost of revenues
Materials and finished products		$	502		$	268
Stock-based compensation			33			25
Compensation and benefits			299			384
Depreciation and amortization			217			217
Equipment, production and other expenses			303			432
Total cost of revenues		$	1,354		$	1,326

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Selling, general and administrative expenses. The following table highlights selling, general and administrative expenses by type for the nine months ended September 30, 2018 and 2017 (in thousands):

	Nine Months Ended September 30,
	2018			2017
Selling, general and administrative expenses
Compensation and benefits		$	301		$	151
Stock-based compensation			173			158
Professional fees			715			289
Other expenses and professional fees			544			177
Total selling, general and administrative expenses		$	1,733		$	775

Selling, general and administrative expenses increased by $0.9 million to $1.7 million for the nine months ended September 30, 2018, as compared to $0.8 million for the nine months ended September 30, 2017. The increase in selling, general and administrative expenses is directly attributable to higher professional fees related to legal and consulting fees.

Compensation and benefits increased by $0.1 million to $0.3 million for the nine months ended September 30, 2018, as compared to $0.2 million for the nine months ended September 30, 2017. The increase in compensation and benefits was primarily due the change in employees’ roles and allocation in 2018 compared to 2017.

Stock-based compensation increased by a nominal amount for the nine months ended September 30, 2018, as compared the nine months ended September 30, 2017. The increase in stock-based compensation is primarily due to a change in stock price in 2018 compared to 2017.

Other expenses and professional fees increased by $0.8 million to $1.3 million for the nine months ended September 30, 2018 from $0.5 million for the nine months ended September 30, 2017. Other selling, general and administrative expenses consist of costs associated with our selling efforts and general management, including information technology, travel, training and recruiting. The increase was due to higher legal and consulting expenses.

Off Balance Sheet Arrangements

As of September 30, 2018, we had no off-balance sheet arrangements in the nature of guarantee contracts, retained or contingent interests in assets transferred to unconsolidated entities (or similar arrangements serving as credit, liquidity or market risk support to unconsolidated entities for any such assets), or obligations (including contingent obligations) arising out of variable interests in unconsolidated entities providing financing, liquidity, market risk or credit risk support to us, or that engage in leasing, hedging or research and development services with us.

Critical Accounting Policies

Our critical accounting policies are described in the notes to our financial statements for the year ended December 31, 2017 and included elsewhere herein.

Recent Accounting Pronouncements

Recently issued accounting pronouncements are addressed in Note 1 in the notes to our financial statements for the year ended December 31, 2017 and included elsewhere herein.

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MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND PLAN OF OPERATION OF TOP

Forward-Looking Statements

The following discussion contains management’s discussion and analysis of TOP’s financial condition and results of operations and TOP’s plan of operation and should be read together with “Selected Historical Consolidated Financial Data for TOP” and the historical consolidated financial statements and the notes thereto included herein. This discussion contains forward-looking statements that reflect TOP’s plans, estimates and beliefs and involve numerous risks and uncertainties, including but not limited to those described in the “Risk Factors” section hereof. Actual results may differ materially from those contained in any forward-looking statements. These statements are based on information available to us as of the date hereof and while we believe that information provides a reasonable basis for these statements, that information may be limited or incomplete. TOP’s statements should not be read to indicate that it has conducted an exhaustive inquiry into, or review of, all relevant information. These statements are inherently uncertain, and you are cautioned not to unduly rely on these statements. You should not rely upon forward-looking statements or forward-looking information as predictions of future events. Furthermore, such forward-looking statements or forward-looking information speak only as of the date hereof. Except as required by law, TOP undertakes no obligation to update any forward-looking statements or forward-looking information to reflect events or circumstances after the date of such statements. You should carefully read “Cautionary Statement Concerning Forward-Looking Statements” and “Risk Factors.”

Overview

TOP is an early stage company with no revenues from operations. There is substantial doubt that TOP can continue as an on-going business for the next twelve months without raising additional capital. TOP does not anticipate that it will generate revenues from its research and development activities related to its drug development projects in the near future, due to the protracted revenue model of pursuing pharmaceutical drug development in accordance with the pathway set forth by the FDA and non-U.S. regulatory authorities.

As a relatively new business engaged in start-up operations and activities, TOP will require substantial additional funding to successfully complete any of its drug development programs. At present, TOP cannot estimate the substantial capital requirements needed to secure regulatory approvals for its drug candidates. Nevertheless, TOP estimates that it will need to raise at a minimum $2 million during the next 12 months to continue its drug development programs and fund the operating costs related to being a public company. Determining a budget is subject to a number of factors. In general, this estimate may be higher if our research efforts prove to be successful, or lower if the research efforts produce results that warrant a decision to cease ongoing research and development efforts. Failure to obtain this necessary capital at acceptable terms, if at all, when needed, may force TOP to delay, limit, or terminate its drug development efforts to secure regulatory approvals and would adversely impact its planned research and development efforts in connection with the Company’s future drug candidates, which may make it more difficult for TOP to attain profitability.

Pursuant to the Merger Agreement, TOP will merge with and into Merger Sub with TOP as the surviving company and following the Merger, will become a wholly owned subsidiary of AquaMed, subject to the terms and conditions in the Merger Agreement. The current members of TOP and other third-party investors in AquaMed will receive approximately 90% of the total number of shares of AquaMed common stock outstanding immediately after the Merger and the proposed concurrent Private Placement, before giving effect to any fees payable in equity to financial advisors or other intermediaries. After giving effect to the Merger and the proposed distribution to the stockholders of Alliqua, Inc. of the shares of common stock of AquaMed owned thereby, AquaMed expects to have a class of equity securities publicly traded on the Nasdaq Capital Market, which it believes will enhance its and TOP’s access to capital; however, no assurance can be given that AquaMed or TOP will successfully raise capital on terms that will permit the successful execution of its business plan.

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Results of Operations for the nine months ended September 30, 2018 and 2017

Net loss for the nine months ended September 30, 2018 was ($636,888), an increase of $112,130 or 21% from the net loss of ($524,758) for the nine months ended September 30, 2017, as a result of an increase of $266,287 or 360% in research and development expenses from the corresponding period in 2017 due to TOP’s escalating research and development activities, which more than offset a decrease of $154,157 or 34% in selling, general and administrative expenses, which resulted primarily from a $125,308 or 49% decrease in professional fees.

Professional fees consisted primarily of legal fees to external counsel for patent and related development matters. During the period ended September 30, 2018, the Company’s efforts were focused on filings with the U.S. and non-U.S. patent offices and the development of protocols and investigative brochures, and the payment of fees to members of the medical advisory board and consultants for scientific development.

Results of Operations for the years ended December 31, 2017 and 2016

Net loss for the years ended December 31, 2017 was ($737,670), a decrease of $322,725 or 30% from the net loss of ($1,060,395) for the year ended December 31, 2016, as a result of decreased selling, general and administrative expenses, which resulted primarily from a $335,069 or 55% decrease in professional fees. This decrease more than offset an increase of $128,917 in research and development expenses from the 2017 period.

Professional fees consisted primarily of legal fees to external counsel for patent and related development matters. During the year ended December 31, 2018, the Company’s efforts were focused on filings with the U.S. and non-U.S. patent offices and the development of protocols and investigative brochures, and the payment of fees to members of the medical advisory board and consultants for scientific development.

Liquidity and Capital Resources

At September 30, 2018, TOP had no cash. In November 2018, TOP raised $500,000 in connection with which it issued $500,000 principal amount of 5% convertible promissory notes due March 31, 2019 (the “Bridge Notes”). For the nine-month period ended September 30, 2018, TOP used net cash in operating activities of $404,626, and for the year ended December 31, 2017, TOP used net cash in operating activities of $625,393, which it funded by borrowing such amount from an affiliate pursuant to a master services agreement. On September 26, 2018, TOP agreed to permit the affiliate to convert its aggregate $1,036,256 obligations under the master services agreement into up to six percent (6%) of the fully diluted equity of TOP.

In November 2018, TOP issued $500,000 principal amount of Bridge Notes to four accredited investors. The Bridge Notes bear interest at a rate of 5% per annum, payable upon maturity at March 31, 2019. The Bridge Notes convert automatically upon consummation of the Merger at a conversion price equal to 80% of the per share price in the Private Placement.

The Company entered into five agreements to conduct clinical trials in Israel, pursuant to which it is obligated to pay an aggregate of approximately $633,000, of which approximately $137,000 was paid as of September 30, 2018 and approximately $496,000 remained owing as of such date.

TOP’s ability to create sufficient working capital to sustain it over the next twelve-month period, and beyond, is dependent on it raising additional equity or debt capital, or entering into strategic arrangements with one or more third parties. While management of the TOP believes that TOP will be successful in its current and planned activities, there can be no assurance that sufficient capital will be available to TOP, that TOP will be successful in efforts to raise sufficient equity or debt capital, that the terms of any financing transaction will be favorable to TOP, or that TOP will engage in strategic relationships, in the aggregate sufficient to sustain the operations of TOP. There is also no assurance that TOP’s drug candidate development activities will be successful in the short term or the long term in generating revenues from operations sufficient to sustain its operations.

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TOP currently has no agreements, arrangements or understandings with any person to obtain funds through bank loans, lines of credit or any other sources.

Notwithstanding TOP’s proposed capital raise from the private sale of equity securities concurrent with the Merger, there can be no assurance that TOP will continue to be successful in raising equity capital and have adequate capital resources to fund its operations or that any additional funds will be available to TOP on favorable terms or in amounts required by TOP. TOP estimates that it will need to raise at a minimum $2 million during the next 12 months to continue its drug candidate development projects and fund the operating costs related to being a public company. Determining a budget is subject to a number of factors. In general, this estimate may higher if TOP’s research efforts prove to be successful or lower if the research efforts produce results that warrant a decision to cease ongoing research and development efforts. If TOP determines that it is necessary to raise additional funds, it may choose to do so through public or private equity or debt financing, a bank or non-bank loan line of credit, or other arrangements. If TOP is unable to obtain adequate capital resources to fund its operations, it may be required to delay, scale back or eliminate some or all of its planned operations, which may have a material adverse effect on its business, results of operations and ability to operate as a going concern.

Any additional equity financing may be dilutive to stockholders, and new equity securities may have rights, preferences or privileges senior to those of existing common stockholders. Debt or equity financing may subject TOP to restrictive covenants and significant interest costs.

Capital Expenditure Plan During the Next Twelve Months

To date, TOP has not raised significant equity capital. TOP intends to utilize the capital that it raises to fund its ongoing research efforts and administrative costs, including the costs incurred by being a public reporting company. However, there can be no assurance that TOP will be successful in raising capital in sufficient amounts and/or at terms and conditions satisfactory to TOP. TOP’s revenues are expected to come from its drug candidate development programs. As a result, TOP expects to continue to incur operating losses unless and until it obtains regulatory approval with respect to one or more of its drug candidate development projects and is able to market and sell such approved products sufficient to generate sufficient cash flow to meet operating expenses. There can be no assurance that TOP will obtain regulatory approval or that the market will adopt its anticipated future drug products. In the event that TOP is not able to successfully: (i) raise equity capital and/or debt financing; or (ii) market its drugs after obtaining regulatory approval, its financial condition and results of operations will be materially and adversely affected.

Going Concern Consideration

Off-Balance Sheet Arrangements

As of September 30, 2018 and December 31, 2017, TOP did not have any off-balance sheet arrangements as defined in Item 303(a)(4)(ii) of Regulation S-K promulgated under the Securities Act of 1934.

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Contractual Obligations and Commitments

Management Agreements

TOP has entered into an offer letter agreement dated October 19, 2018 with Seth Yakatan to serve as its chief executive officer for an annual salary of $150,000. Mr. Yakatan is also eligible to receive options for three percent (3%) of AquaMed’s outstanding stock after giving effect to the Merger and the Private Placement.

TOP has entered into a consulting agreement dated as of November 1, 2018 with Broom Street Associates to provide the services of Dr. Mitchell Glass as TOP’s chief medical officer, at an annual rate of $120,000, payable half in cash and half in equity.

TOP entered into an employment agreement dated March 9, 2016 with Sidney Taubenfeld to serve as an executive vice president of TOP for an annual salary of $168,000. TOP has also issued warrants to Mr. Taubenfeld to purchase 39,505 Class A Units, of which 28,218 are vested as of September 30, 2018, at an exercise price of $12.40 per Class A Unit, which after the Merger will be exercisable for 737,894 shares of common stock, of which approximately 527,067 are vested as of September 30, 2018, at an exercise price of $0.66 per share.

TOP has issued a warrant to Bernard Sucher, a manager of TOP, which is exercisable for an aggregate of 11,187 Class A Units, half of which are exercisable at exercise prices of $15.11 and $45.32 per Class A Unit, which after the Merger will be exercisable for 208,959 shares of common stock, half of which are exercisable at exercise prices of $.81 and $2.43 per share.

U.S. and Worldwide Pharmaceutical Licenses with TOL

Pursuant to the MOU (i) TOPUSA entered into the US Pharma License; and (ii) TOIP the WW Pharma License. Pursuant to the Pharma Licenses, TOL granted an exclusive, perpetual, non-revocable, royalty-free and sublicensable license to use TOL’s intellectual property, whenever developed, in connection with the TOP’s Pharmaceutical Business. TOPUSA is permitted to use such intellectual property solely in the United States and TOIP is permitted to use such intellectual property anywhere in the world excluding the United States.

Sublicenses

TOPUSA and Tikkun Pharma have entered into the TP USA Sublicense Agreement, and TOIP and Tikkun Pharma have entered into TP WW Sublicense Agreement, pursuant to which TOPUSA and TOIP each have granted a perpetual, non-revocable (subject to the terms of the TP Sublicense Agreements), fully paid, royalty-free, exclusive sublicense of TOL’s intellectual property and license of their respective intellectual property, in their respective territories, in connection with the TP Limited Business. TOP received a 50% ownership interest in Tikkun Pharma. Tikkun Pharma has failed to fulfill certain of its obligations to TOP, with respect to which TOP has not exercised any remedial action.

TOPUSA and Jay Pharma have entered into the JP USA Sublicense Agreement, and TOIP and Jay Pharma have entered into (the JP WW Sublicense Agreement, pursuant to which TOPUSA and TOIP each have granted a perpetual, non-revocable (subject to the terms of the JP Sublicense Agreements), fully paid, royalty-free, exclusive sublicense of TOL’s intellectual property and license of their respective intellectual property, in their respective territories, in connection with the JP Limited Business. TOP received a 50% ownership interest in Jay Pharma.

Clinical Trials Agreements

TOP has entered into the MOR Agreement to examine and use Avidekel, a proprietary cannabis plant of TOL to which TOP holds intellectual property rights, with respect to the treatment of patients with inflammatory bowel diseases (“IBD”). The goal of such examination and use is to achieve a written study that can be utilized to create an IBD-based treatment or drug approved by the applicable drug administration(s). Pursuant to the MOR Agreement, (a) TOP is obligated to pay to MOR (i) for the 80 subjects taking part in this study, an amount of US$120,000 (US$1,500 per subject), and (ii) an annual

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amount equal to 8% of TOP’s net revenues generated and actually received by TOP from the sale of the IBD drug to the public for the treatment of IDB; and (b) TOP retains all right, title and interest in and to all intellectual property and derivatives, modifications, enhancements and improvements thereto.

TOP has entered into the Lanaido Agreement to conduct a study focused on evaluating the safety and efficacy of Avidekel oil for the treatment of subjects with agitation related to Alzheimer’s and other forms of dementia. Pursuant to the Lanaido Agreement, (a) TOP is obligated to pay to Lanaido approximately $115,000; (b) TOP retains all right, title and interest in and to all intellectual property subject to the Lanaido Agreement; and (c) TOP is permitted to publish the results of and information pertaining to the study, whether, for any scientific, commercial or promotional purposes, at any time.

TOP has entered into the Soroka Agreement to conduct a double-blind placebo controlled, randomized trial in order to assess the safety and efficacy of medical grade cannabis oil derived from the cannabis strain Erez in acute migraine patients. Pursuant to the Soroka Agreement, (a) TOP is obligated to pay to Soroka an amount equal to US$200,000, which is due in installments based upon the achievement of certain thresholds, including a fee per subject of US$1,927 for up to 88 subjects, (b) TOP retains all right, title and interest in and to all intellectual property subject to the Soroka Agreement; and (c) TOP is permitted to publish the results of and information pertaining to the study, whether, for any scientific, commercial or promotional purposes, at any time.

TOP has entered into the Assaf Harofeh Agreement to conduct a randomized, double-blind, placebo controlled, parallel-group, pilot study in order to investigate the safety and efficacy of medical grade cannabis oil derived from the strain Midnight in the maintenance hemodialysis patients with protein-energy wasting (“PEW”). Pursuant to the Assaf Harofeh Agreement, (a) TOP is obligated to pay to Assaf Harofeh an amount equal to approximately US$137,000, (b) TOP retains all right, title and interest in and to all intellectual property subject to the Assaf Harofeh Agreement; and (c) TOP is permitted to publish the results of and information pertaining to the study, whether, for any scientific, commercial or promotional purposes, at any time.

TOP has entered into the Sheba Agreement to conduct a study in order to assess the use of THC in medical grade cannabis oil derived from the strain Erez in benign essential blepharospasm (“BEB”). Pursuant to the Sheba Agreement, (a) TOP is obligated to pay to Sheba Fund an amount equal to US$61,000, which is due on a per subject and per visit basis for up to 20 subjects, (b) TOP retains all right, title and interest in and to all intellectual property subject to the Sheba Agreement; and (c) TOP is permitted to publish the results of and information pertaining to the study, whether, for any scientific, commercial or promotional purposes, at any time.

Contingencies

In the normal course of business, TOP may receive inquiries or become involved in legal disputes regarding various litigation matters. In the opinion of management, any potential liabilities resulting from such claims would not have a material adverse effect on TOP’s consolidated financial statements.

Critical Accounting Policies

Our significant accounting policies are described in the notes to our financial statements as of December 31, 2017 and included elsewhere herein.

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LIQUIDITY AND CAPITAL RESOURCES FOLLOWING THE TRANSACTIONS

The following discussion and analysis intended to help prospective investors understand our liquidity and capital resources following the transactions. You should read this discussion in conjunction with our combined financial statements and related notes thereto included elsewhere in this prospectus.

The statements in this discussion are forward-looking statements. These forward-looking statements are subject to numerous risks and uncertainties, including, but not limited to, the risks and uncertainties described in “Risk Factors” and “Special Note Regarding Forward-Looking Statements.” Actual results may differ materially from those contained in any forward-looking statements.

Immediately following the Merger, we expect to have no cash except the remaining proceeds of the Private Placement, which we believe will be sufficient to fund our operations for at least twelve months, including continued funding of its drug candidate development projects, any operating losses and funding the operating costs related to being a public company. For the nine-month period ended September 30, 2018, TOP used net cash in operating activities of $404,626, and for the year ended December 31, 2017, TOP used net cash in operating activities of $625,393, which it funded by borrowing such amount from TOG. On September 26, 2018, TOP agreed to permit TOG to convert its aggregate $1,036,256 obligations into up to six percent (6%) of the fully diluted equity of TOP, which TOG has done.

For the nine-month period ended September 30, 2018, AquaMed used net cash in operating activities of $1.2 million, and for the year ended December 31, 2017, AquaMed used net cash in operating activities of .8 million, which was funded by Alliqua.

In November 2018, to fund its working capital needs and transaction expenses relating to the Merger, TOP issued $500,000 principal amount of 5% convertible promissory notes (the “Bridge Notes”) to four accredited investors. The Bridge Notes bear interest at a rate of 5% per annum, payable upon maturity at March 31, 2019. The Bridge Notes convert automatically upon consummation of the Merger at a conversion price equal to 80% of the per share price in the Private Placement.

Neither TOP nor AquaMed has any material commitments for capital expentitures. TOP has entered into five agreements to conduct clinical trials in Israel, pursuant to which it is obligated to pay an aggregate of approximately $633,000, of which approximately $137,000 was paid as of September 30, 2018 and approximately $496,000 remained owing as of such date. After giving effect to the Merger, these will be the primary obligations of the Company other than ordinary course expenses.

We currently have no agreements, arrangements or understandings with any person to obtain funds through bank loans, lines of credit or any other sources. Our ability to create sufficient working capital to sustain the Company over the next twelve-month period, and beyond, is dependent on raising additional equity or debt capital or entering into strategic arrangements with one or more third parties. While our management believes that we will be successful in our current and planned activities, there can be no assurance that sufficient capital will be available to us, that we will be successful in efforts to raise sufficient equity or debt capital, that the terms of any financing transaction will be favorable to us, or that we will engage in strategic relationships, in the aggregate sufficient to sustain our operations. There is also no assurance that our hydrogel manufacturing operations will operate profitably or that our drug candidate development activities will be successful in the short term or the long term in generating revenues from operations sufficient to sustain our operations.

In general, our estimated cash needs may be higher if our research efforts prove to be successful or lower if the research efforts produce results that warrant a decision to cease ongoing research and development efforts. If we determine that it is necessary to raise additional funds, we may choose to do so through public or private equity or debt financing, a bank or non-bank loan line of credit, or other arrangements. If we are unable to obtain adequate capital resources to fund our operations, we may be required to delay, scale back or eliminate some or all of our planned operations, which may have a material adverse effect on our business, results of operations and ability to operate as a going concern.

Any additional equity financing may be dilutive to stockholders, and new equity securities may have rights, preferences or privileges senior to those of existing common stockholders. Debt or equity financing may subject us to restrictive covenants and significant interest costs.

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Capital Expenditure Plan During the Next Twelve Months

To date, we have not raised significant equity capital. We intend to utilize any capital that we raise to fund our ongoing research efforts and administrative costs, including the costs incurred by being a public reporting company. However, there can be no assurance that we will be successful in raising capital in sufficient amounts and/or at terms and conditions satisfactory to us. Our revenues are expected to come from our hydrogel manufacturing business and drug candidate development programs. As a result, we expect to continue to incur operating losses unless and until we obtain regulatory approval with respect to one or more of our drug candidate development projects and may be able to market and sell such approved products sufficient to generate sufficient cash flow, in addition to cash flow generated by the hydrogel manufacturing business, to meet operating expenses. There can be no assurance that we will obtain regulatory approval or that the market will adopt our anticipated future drug products, or that our hydrogel manufacturing business will be profitable. In the event that we are not able to successfully: (i) raise equity capital and/or debt financing; or (ii) market our drugs after obtaining regulatory approval, or (iii) operate our hydrogel manufacturing business profitably, our financial condition and results of operations will be materially and adversely affected.

Going Concern Consideration

For the fiscal year ended December 31, 2017, TOP recorded a net loss of ($737,670) and used cash in operating activities of $625,393. For the nine-month period ended September 30, 2018, TOP recorded a net loss of ($636,888), and used cash in operations of $404,626. For the nine-month period ended September 30, 2018, AquaMed used net cash in operating activities of $1.2 million, and for the fiscal year ended December 31, 2017, AquaMed used net cash in operating activities of $.8 million, which was funded by Alliqua, which funding will no longer be available. TOP has incurred losses since inception, resulting in a members’ equity deficit of $2,434,853 as of September 30, 2018. AquaMed has also historically generated losses from operations. In light of, among other things, TOP’s and AquaMed’s working capital deficits, lack of available cash and cash equivalents and history of operating losses, in order to remain in business and maintain its drug development activities, the Company must raise capital from sources other than the actual sale from any drugs that it may develop, as it is unlikely that profits from the Company’s hydrogel manufacturing business, if any, would be sufficient to sustain the Company’s cash flow needs. Accordingly, there is substantial doubt about whether the Company will be able to continue as a going concern. The reports of TOP’s and AquaMed’s independent registered public accounting firm with respect to their financial statements at December 31, 2017, and for the year ended December 31, 2017, each contain an explanatory paragraph as to TOP’s and AquaMed’s respective potential inability to continue as a going concern. These opinions indicate that substantial doubt exists regarding TOP’s and AquaMed’s ability to remain in business. Such an opinion may adversely affect the surviving company’s’s ability to obtain new financing on reasonable terms or at all.

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MANAGEMENT OF THE COMPANY FOLLOWING THE TRANSACTIONS

The following table presents information concerning the individuals who are expected to serve as our executive officers and directors, and their anticipated titles, following the Spin-Off and Merger, including a brief summary of the business experience of each of them. We are in the process of identifying additional executive officers and directors and we expect to provide details in an amendment to this prospectus.

Name	Age	Position
Executive Officers
Seth Yakatan	48	Chief Executive Officer
Mitchell Glass	67	Chief Medical Officer
Sidney Taubenfeld	58	Vice President
Directors
David Johnson	60	Chairman of the Board of Directors
Berel Farkas	30	Director

Executive Officers

Seth Yakatan, Chief Executive Officer

Mr. Yakatan has served as chief executive officer of TOP since October 2018. Mr Yakatan has served as a director of FitLife Brands, Inc. and iSatori, Inc., which was acquired by FitLife Brands, Inc., since September 2014. He also served as interim Chief Financial Officer of iSatori, Inc. from April 2015 until the its merger with FitLife Brands. Mr. Yakatan served as interim CEO of Kalytera Therapeutics, Inc. from December 2015 through January 2017, and also served as a director thereof from December 2015 through July 2017. Mr. Yakatan and is a founder of Katan Associates, a consulting firm. Mr. Yakatan brings more than 24 years of experience as a life sciences business development and corporate finance professional, actively supporting small cap and major companies in achieving corporate, financing, and asset monetization objectives. Mr. Yakatan began his career as a venture capital analyst with Ventana Growth Funds and Sureste Venture Management, where he gained significant experience in creating successful venture-backed life science and biotechnology companies. Prior to founding Katan Associates in 2001, Mr. Yakatan worked in merchant banking at Union Bank of California, N.A., in the Specialized Lending Media and Telecommunications Group. During his six years there, he completed the placement of subordinated debt and private equity investments, exceeding $3 billion in transaction value. Mr. Yakatan holds an MBA in Finance from the University of California, Irvine, and a BA in History and Public Affairs from the University of Denver.

Mitchell Glass, Chief Medical Officer

Dr. Mitchell Glass has served as TOP’s chief medical officer since November 2018. Since November 2012, Dr. Glass has served as an executive director and as executive vice president of research and development of Invion Ltd (ASX: IVX). Since August 2013, Dr. Glass has served as the chairman of the board of Accolade Pharmaceuticals LLC, a privately held specialty pharmaceutical company. Since October 2017, Dr. Glass has served as the chief medical officer of Strados Labs LLC, a privately held medical device and services developer. Since 2010, Dr. Glass has also served as the manager of Broom Street Associates LLC, a consulting firm to early stage pharmaceutical and medical device companies. Dr. Glass holds an M.D (1977) and an A.B (1973), with special honors in biology, from the University of Chicago.

Sidney Taubenfeld

Sidney Taubenfeld has served as President of TOP since March 2016. Mr. Taubenfeld started his career as a clinical pharmacist at Bellevue Hospital before becoming buy-side healthcare equities research analyst and portfolio manager. For more than three years prior thereto, he worked at Scopia Capital, PAW Partners, Balyasny Asset Management (BAM), RH Capital, and Celsion Corporation. Mr. Taubenfeld received a B.S. from the Brooklyn College of Pharmacy and did graduate work in Pharmacology at New York Medical College.

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Board of Directors

David I. Johnson, Chairman of the Board of Directors

Mr. Johnson has served on the board of directors of Alliqua since November 2012 and has served as the President and Chief Executive Officer of Alliqua since February 2013. Mr. Johnson was formerly President of the ConvaTec Division of Bristol-Myers Squibb, Inc. until 2008 when he orchestrated a sale of the division from its pharmaceutical parent to Avista Capital Partners and Nordic Capital in a deal valued at $4.1 billion. Concurrently, he acquired and integrated the assets of Copenhagen-based Unomedical to expand ConvaTec Inc.’s manufacturing and infrastructure into Europe. From 2008 through 2012, Mr. Johnson served as the Chief Executive Officer of ConvaTec Inc. Prior to his tenure with ConvaTec Inc., Mr. Johnson held several senior positions in the U.S., Europe and Canada with Zimmer Inc., Fisher Scientific, and Baxter Corporation. He served as a member of ConvaTec Inc.’s board of directors and the board of the Advanced Medical Technology Association (AdvaMed), where he chaired the Global Wound Sector Team for four years. Mr. Johnson received an Undergraduate Business Degree in Marketing from the Northern Alberta Institute of Technology in Edmonton, Alberta, Canada, completed the INSEAD Advanced Management Program in Fontainbleau, France, and is a fellow from the Wharton School of the University of Pennsylvania. Mr. Johnson’s extensive experience in the pharmaceutical and biotechnology fields, as well as his executive leadership experience, make him an asset that will serve as a bridge between the board of directors and our executive officers.

Berel (“Barry”) Farkas, Director

Berel (Barry) Farkas has served as a Manager of TOP since July 2018, and as a Manager of TOG since June 2015, and as Chairman of the Board thereof since July 2016. Since 2011, Mr. Farkas has served as a partner of Lightstone Management, LLC, a real estate investment firm.

Our Board of Directors Following the Spin-Off and Director Independence

Immediately following the Spin-Off, we expect that our Board of Directors will comprise five (5) directors. The corporate governance standards of the Nasdaq Capital Market require that the board have a majority of independent directors, and we expect our Board of Directors to include a majority of independent directors and board committees composed of the requisite number of independent directors at the time of the Spin-Off under the corporate governance standards of the Nasdaq Capital Market and the independence requirements of Rule 10A-3 of the Exchange Act.

Effective upon the completion of the Spin-Off, our Board of Directors will have the following committees, each of which will operate under a written charter that will be posted on our website immediately prior to the Spin-Off.

Audit Committee

The Audit Committee will be established in accordance with Section 3(a)(58)(A) and Rule 10A-3 under the Exchange Act. The responsibilities of our Audit Committee will be more fully described in our Audit Committee charter. We anticipate that our Audit Committee will, among other duties:

•

oversee financial reporting, accounting, control and compliance matters;

•

appoint and evaluate the independent auditor;

•

review with the internal and independent auditors the scope, results and adequacy of their audits and effectiveness of internal controls;

•

review material financial disclosures;

•

pre-approve all audit and permitted non-audit services;

•

annually review our compliance programs and receive regular updates about compliance matters;

•

annually review our disclosure controls and procedures; and

•

review and make recommendations to our Board of Directors about related-person transactions.

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The Audit Committee will have at least three members and will include a requisite number of directors that will meet the independence requirements set forth in the listing standards of the Nasdaq Capital Market, Rule 10A-3 under the Exchange Act and our Audit Committee charter. Each member of the Audit Committee will be financially literate, and at least one member of the Audit Committee will have accounting and related financial management expertise and satisfy the criteria to be an “audit committee financial expert” under the rules and regulations of the SEC, as those qualifications will be interpreted by our Board of Directors in its business judgment. The initial members of the Audit Committee will be determined prior to the Spin-Off.

Compensation Committee

The responsibilities of our Compensation Committee will be more fully described in our Compensation Committee charter, and we anticipate that they will include, among other duties:

•

approving and recommending full Board of Directors approval of the CEO’s compensation based upon an evaluation of the CEO’s performance by the independent directors;

•

reviewing and approving senior management’s compensation;

•

administering incentive and equity compensation plans and, in consultation with senior management, approving compensation policies; and

•

reviewing executive compensation disclosures and the annual compensation risk assessment.

The Compensation Committee will include a requisite number of directors that will meet the independence requirements set forth in the listing standards of the Nasdaq Capital Market, Rule 10C-1 under the Exchange Act and our Compensation Committee charter. The members of the Compensation Committee will be “non-employee directors” (within the meaning of Rule 16b-3 under the Exchange Act) and “outside directors” (within the meaning of Section 162(m) of the Code (“Section 162(m)”)). The initial members of the Compensation Committee will be determined prior to the Spin-Off.

Nominating/Corporate Governance Committee

The responsibilities of our Nominating/Corporate Governance Committee will be more fully described in our Nominating/Corporate Governance Committee charter, and we anticipate that they will include, among other duties:

•

monitoring our Board of Directors’ structure and operations;

•

setting criteria for Board of Directors membership;

•

searching for and screening candidates to fill Board of Directors vacancies and recommend candidates for election;

•

evaluating director and Board of Directors performance and assess Board of Directors composition and size;

•

evaluating our corporate governance process; and

•

recommending to our Board of Directors whether to accept the resignation of incumbent directors that fail to be re-elected in uncontested elections.

The Nominating/Corporate Governance Committee will include a requisite number of directors that will meet the independence requirements set forth in the listing standards of the Nasdaq Capital Market and our Nominating/Corporate Governance Committee charter. The initial members of the Nominating/Corporate Governance Committee will be determined prior to the Spin-Off.

Codes of Conduct

We are committed to high standards of ethical conduct and professionalism. Prior to the completion of the Spin-Off, we will adopt a Code of Business Conduct that confirms our commitment to ethical behavior in the conduct of all our activities. The Code of Business Conduct will apply to all our directors, all our officers (including our CEO, CFO and Principal Accounting Officer) and employees and it will set forth our

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policies and expectations on a number of topics including avoiding conflicts of interest, confidentiality, insider trading, protection of AquaMed and customer property and providing a proper and professional work environment. We expect to continue to follow the same corporate governance practices immediately following the Distribution.

Director Nomination Process

Our initial Board of Directors will be selected through a process involving TOP and us. We intend to adopt corporate governance principles designed to assure excellence in the execution of the Board of Directors’ duties. These principles will be outlined in Corporate Governance Guidelines which, in conjunction with our Amended and Restated Articles of Incorporation, Amended and Restated Bylaws, Code of Business Conduct, Board of Directors committee charters and related policies will form the framework for the effective governance of AquaMed. Our Corporate Governance Guidelines will be available on our website prior to the Spin-Off.

Communicating with the Board or Chairman

After the Spin-Off, stockholders and other interested parties may communicate with the Board of Directors, individual directors, the non-management directors as a group, or with the Chairman, by writing in care of the Corporate Secretary, AquaMed Technologies, Inc., 2150 Cabot Boulevard West, Suite B, Langhorne, PA 19047. The Corporate Secretary will review all submissions and forward to members of the Board of Directors all appropriate communications that in the Corporate Secretary’s judgment are not offensive or otherwise objectionable and do not constitute commercial solicitations.

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EXECUTIVE COMPENSATION

Summary

This section discusses the anticipated compensation to be paid by us to our executive officers following the Spin-Off and Merger for our fiscal year beginning January 1, 2019 and ending December 31, 2019 (“Fiscal 2019”).

Historical Compensation of Executive Officers Prior to the Spin-Off

Mr. Johnson served as AquaMed’s chief executive officer during its last completed fiscal year and Joseph Warusz served as its chief financial officer during its last completed fiscal year beginning on April 1, 2018. From January 1, 2018 through March 30, 2018, Brian Posner served as the chief financial officer of AquaMed. None of Mr. Johnson, Mr. Warusz or Mr. Posner received any compensation for their service as executive officers of AquaMed during its last completed fiscal year. Mr. Yakatan, Dr. Glass and Mr. Taubenfeld were not employed by AquaMed prior to the Spin-Off and Merger and therefore none of their historical compensation is discussed in this section.

Executive Officers and Compensation Going Forward

Expected AquaMed Executive Officers

Following the Spin-Off and Merger, we expect the following individuals to become our executive officers:

•

Seth Yakatan, who is currently the Chief Executive Officer of TOP, is expected to become our Chief Executive Officer;

•

Mitchell Glass, who is currently the Chief Medical Officer of TOP, is expected to serve as our Chief Medical Officer; and

•

Sidney Taubenfeld, who is currently the President of TOP, is expected to serve as our vice president.

Following the Spin-Off, we will form our own board-level compensation committee (our “Compensation Committee”) that will be responsible for approving and overseeing our executive compensation programs. We expect to adopt a long-term equity-based incentive program and to offer post-employment benefits and severance programs similar to the programs that existed at Alliqua prior to the Spin-Off. Following the Spin-Off, our Compensation Committee will review and monitor the effect of the Spin-Off and the Merger on our executive compensation programs, and may make any adjustments it deems appropriate based on the Spin-Off or Merger or any other factors.

Fiscal 2019 Expected AquaMed Compensation

The recommended compensation levels for the individuals who are expected to become our named executive officers for periods after the Spin-Off and Merger are as follows:

Name and principal position	Salary			Annual Incentive Target(1)		Long Term Incentive Target(1)		Target Total Direct Compensation(1)
Seth Yakatan		$	150,000		—		—		—
Dr. Mitchell Glass		$	120,000		—		—		—
Sidney Taubenfeld		$	168,000		—		—		—

(1)

Does not include options, warrants or other securities issued or granted to the named executive officers. See “Security Ownership of Certain Beneficial Owners, Directors and Executive Officers.”

Following the Spin-off, our Board of Directors, with the assistance of the Compensation Committee, expects to consider appropriate annual and long-term incentive targets and total compensation packages for our executive officers.

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Treatment of Outstanding Alliqua Equity Awards

Any outstanding Alliqua employee equity awards will be unaffected by the Spin-Off and the Merger. Any Alliqua equity awards held by individuals who are or become our employees in connection with the Spin-Off (including Mr. Johnson) will not see any adjustment in connection with the Spin-Off and/or the Merger.

AquaMed Employee Equity Plan

We expect to adopt an equity incentive plan (the “AquaMed Employee Equity Plan”) prior to the Spin-Off and Merger for the purpose of allowing us to grant equity and equity-based incentive awards to our eligible employees following the Spin-Off and the Merger. We expect to reserve approximately 2,000,000 shares of our common stock for issuance under the plan. The number of reserved shares would be subject to future adjustments to reflect any future stock splits, reverse stock splits, stock dividends, subdivisions, consolidations, recapitalizations, reorganizations, mergers and other similar events, as determined in the plan administrator’s discretion.

We expect the terms of the AquaMed Employee Equity Plan to allow us to grant incentive stock options, nonqualified stock options, stock appreciation rights, restricted stock, restricted stock units, performance awards and other awards which may be granted singly, in combination, or in tandem, and which may be paid in cash or shares of common stock. All of our employees would be eligible to participate in the plan.

Our Compensation Committee would have broad authority to grant awards and otherwise administer the AquaMed Employee Equity Plan. The plan would become effective upon the effective time of the Spin-Off and would continue in effect for a period of 10 years thereafter, unless earlier terminated by our Board of Directors. Our Board of Directors would have the authority to amend the plan in such respects as it deemed desirable, provided that any amendments that would increase the share reserve (other than pursuant to a recapitalization event described above), expand the class of persons eligible to participate in the plan or the types of awards available for grant under the plan, or that would otherwise be considered a material modification for purposes of applicable tax or securities laws or exchange listing requirements, would require the approval of our stockholders.

The form and terms of the plan are still under evaluation, and we expect to provide details in an amendment to this prospectus.

Employment Agreements

On the Spin-off Date, we expect to enter into an employment agreement with Mr. Yakatan in connection with his service as Chief Executive Officer of AquaMed. The form and terms of our executive compensation program for periods after the Spin-Off and Merger are still under evaluation, and we expect to provide details in an amendment to this prospectus. In addition, any such agreements would be subject to review and approval of our Compensation Committee. Subject thereto:

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CERTAIN RELATIONSHIPS AND RELATED PARTY TRANSACTIONS

AquaMed Agreements with Alliqua

Following the Distribution, Alliqua will not own any of our shares and we will operate independently of Alliqua. In addition, we do not expect to depend on Alliqua to conduct our business following the Distribution. In order to govern the ongoing relationships between us and Alliqua after the Spin-Off, we and Alliqua intend to enter into agreements providing for various rights following the Spin-Off and under which we and Alliqua will agree to indemnify each other against certain liabilities arising from our respective businesses. For a summary of the terms of the material agreements we expect to enter into with Alliqua, see “The Asset Contribution and Separation Agreement and the Ancillary Agreements”. Following the Distribution, our Chairman, Mr. David Johnson will continue serving as a director of Alliqua. Accordingly, transactions with Alliqua may continue to constitute related party transactions under SEC rules and under our related party transactions policy.

TOP

T.O. Global LLC

Until July 13, 2018, TOP was a wholly-owned subsidiary of TOG (“TOG”), which provided funding to TOP pursuant to a master intercompany service agreement (the “Master Services Agreement”), under which TOG advanced funds on behalf of or otherwise extended loans to TOP sufficient to fund TOP’s operations. As of December 31, 2017 and 2016, TOP owed to T.O Global LLC $2,154,310 and $1,528,917, respectively, thereunder. These obligations were unsecured and due on demand with no interest. On September 26, 2018, TOP agreed to permit TOG to convert its aggregate $1,036,256 obligations under the Master Services Agreement into up to six percent (6%) of the fully diluted equity of TOP. In December 2018, TOG exercised this conversion right in full for 39,721 Class A Units.

TOP leases its offices on a month to month basis from TOG. The terms of the lease call for monthly base payments of $1,000. Total rent expense for the years ended December 31, 2017 and 2016 amounted to $12,000, for each of the years.

Management Agreements

U.S. and Worldwide Pharmaceutical Licenses with TOL

Pursuant to the MOU, TOL, which is expected to beneficially own approximately 12% of our outstanding common stock after giving effect to the Merger and the Private Placement, entered into (i) the US Pharma License with TOPUSA; and (ii) the WW Pharma License with TOIP. Pursuant to the Pharma

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Licenses, TOL granted an exclusive, perpetual, non-revocable, royalty-free and sublicensable license to use TOL’s intellectual property, whenever developed, in connection with the TOP’s Pharmaceutical Business. TOPUSA is permitted to use such intellectual property solely in the United States (except the State of New York) and TOIP is permitted to use such intellectual property anywhere in the world excluding the United States. Pursuant to the Pharma Licenses, TOP paid or caused to be paid to TOL an aggregate of $500,000 on behalf of TOPUSA and TOIP. No royalties or other payments are required under the Pharma Licenses except a two percent (2%) royalty payable to TOL with respect to TOIP’s sale of over-the-counter pharmaceutical products outside the U.S. which reasonably compete with a non-pharmaceutical medical cannabis product with substantially similar composition of active components sold by TOL or any licensee of TOL (other than TOIP) conducting business in the applicable jurisdiction pursuant to an effective legal license, permit or similar authority.

Sublicenses

TOPUSA has entered into the TP USA Sublicense Agreement, and TOIP has entered into the TP WW Sublicense Agreement, pursuant to which TOPUSA and TOIP each have granted a perpetual, non-revocable (subject to the terms of the TP Sublicense Agreements), fully paid, royalty-free, exclusive sublicense of TOL’s intellectual property and license of their respective intellectual property, in their respective territories, in connection with the TP Limited Business. TOP received a 50% ownership interest in Tikkun Pharma. Tikkun Pharma has failed to fulfill certain of its obligations to TOP, with respect to which TOP has not exercised any remedial action.

TOPUSA has entered into the JP USA Sublicense Agreement, and TOIP has entered into the JP WW Sublicense Agreement, pursuant to which TOPUSA and TOIP each have granted a perpetual, non-revocable (subject to the terms of the JP Sublicense Agreements), fully paid, royalty-free, exclusive sublicense of TOL’s intellectual property and license of their respective intellectual property, in their respective territories, in connection with the JP Limited Business. TOP received a 50% ownership interest in Jay Pharma.

Related Party Transaction Policy

Our Board of Directors intends to adopt a written policy requiring the approval by the Nominating/Corporate Governance Committee of all transactions in excess of $120,000 between AquaMed and any related person. For the purposes of this policy, a related person is any person who was in any of the following categories at any time during the fiscal year: (i) a director or executive officer of AquaMed; (ii) any nominee for director; (iii) any immediate family member of a director or executive officer, or of any nominee for director (immediate family members are any child, stepchild, parent, stepparent, spouse, sibling, mother-in-law, father-in-law, son-in-law, daughter-in-law, brother-in-law or sister-in-law of such director, executive officer or nominee for director, and any person (other than a tenant or employee) sharing the household of such director, executive officer or nominee for director and any person who was in any of the following categories when a transaction in which such person had a direct or indirect material interest occurred or existed); (iv) any beneficial owner of more than 5% of AquaMed’s common stock; or (v) any immediate family member of any such beneficial owner. A transaction includes, but is not limited to, any financial transaction, arrangement or relationship (including any indebtedness or guarantee of indebtedness) or any series of similar transactions, arrangements or relationships. In determining whether to approve an interested transaction, the Nominating/Corporate Governance Committee will take into account, among other factors it deems appropriate, whether the interested transaction is on terms no less favorable than terms generally available to an unaffiliated third party under the same or similar circumstances and the extent of the related party’s interest in the transaction. No director will participate in any discussion or approval of an interested transaction for which he or she (or an immediate family member) is a related party, except that the director will provide all material information concerning the interested transaction to the Nominating/Corporate Governance Committee. For as long as there are any members of our Board of Directors associated with or employed by Alliqua, each will recuse himself or herself from decisions by our Board of Directors regarding matters relating to Alliqua including matters relating to the agreements between us and Alliqua described above.

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SECURITY OWNERSHIP OF CERTAIN BENEFICIAL OWNERS, DIRECTORS AND
EXECUTIVE OFFICERS

As of the date of this prospectus, Alliqua beneficially owns all the outstanding shares of our common stock. After the Spin-Off, Alliqua will not own any shares of our common stock. The following table provides information regarding the anticipated beneficial ownership of our common stock following consummation of the Spin-Off, the Merger, and all transactions to be consummated in connection therewith or conditioned thereon, by:

•

each of our stockholders who we believe (based on the assumptions described below) will beneficially own more than 5% of our outstanding common stock;

•

each of our directors following the Spin-Off and Merger;

•

each of our executive officers following the Spin-Off and Merger; and

•

all of our directors and executive officers following the Spin-Off and Merger as a group.

Except as otherwise noted below, we based the share amounts on each person’s beneficial ownership of Alliqua common stock on December 31, 2018 or TOP membership units as of December 31, 2018, after giving effect to the exchange ratio set forth in the Merger Agreement and the consummation of the Merger and the transactions contemplated thereby, including the Private Placement.

To the extent our directors and executive officers own Alliqua common stock at the Record Date of the Spin-Off, they will participate in the Distribution on the same terms as other holders of Alliqua common stock.

Except as otherwise noted in the footnotes below, each person or entity identified in the table has sole voting and investment power with respect to the securities he, she or it holds.

Immediately following the Spin-Off, the Merger, and the transactions contemplated thereby, including the Private Placement, we estimate that approximately 17,204,000 shares of our common stock will be issued and outstanding, based on the approximately 5,005,210 shares of Alliqua common stock outstanding on December 31, 2018.

Name and Address of Beneficial Owner(1)	Number of Shares Beneficially Owned(2)		Percentage Beneficially Owned(2)
5% Owners
Tikun Olam Ltd. 183 Ibn Gabirol Street Tel Aviv, 6200715, Israel		2,120,784		12.3%
Tsachi Cohen 183 Ibn Gabirol Street Tel Aviv, 6200715, Israel		2,120,784(3)		12.3%
Menachem Silber 77 Water Street, 8th Floor New York, NY 10005		1,175,961		6.8%
Eric Lerner 77 Water Street, 8th Floor New York, NY 10005		913,664		5.3%
Officers and Directors
Berel Farkas		1,638,932(4)		9.5%
David I. Johnson		119,847(5)		*
Seth Yakatan(6)		—		—
Mitchell Glass		5,385		*

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Name and Address of Beneficial Owner(1)	Number of Shares Beneficially Owned(2)		Percentage Beneficially Owned(2)
Sidney Taubenfeld		527,067(7)		3.0%
All executive officers and directors of the Company, as a group		2,290,512		13.2%

Represents ownership of less than 1%

(1)

Unless otherwise indicated, the address of each person or group is c/o TO Pharmaceuticals, LLC, 77 Water Street, 8th Floor, New York, New York 10005.

(2)

Shares of common stock beneficially owned and the respective percentages of beneficial ownership of common stock assumes the exercise of all options, warrants and other securities convertible into common stock beneficially owned by such person or entity currently exercisable or exercisable within 60 days of January 8, 2019. Shares issuable pursuant to the exercise of stock options and warrants exercisable within 60 days are deemed outstanding and held by the holder of such options or warrants for computing the percentage of outstanding common stock beneficially owned by such person, but are not deemed outstanding for computing the percentage of outstanding common stock beneficially owned by any other person.

(3)

Comprised of 2,120,784 shares of our common stock owned by TOL.

(4)

Comprised of (i) 308,199 shares of our common stock owned directly by Mr. Farkas, and (ii) 1,330,733 shares of our common stock owned by two limited liability companies.

(5)

Based upon 342,814 shares of Alliqua common stock beneficially owned by Mr. Johnson as of December 31, 2018. The address for Mr. Johnson is c/o Alliqua BioMedical, Inc., 2150 Cabot Boulevard, West, Suite B, Langhorne, PA 19067.

(6)

This table does not include options that Mr. Yakatan is eligible to receive, exercisable for three percent (3%) of AquaMed’s outstanding stock after giving effect to the Merger and the Private Placement, which is expected to be an amount equal to approximately 525,000 shares of our common stock and which are not exercisable within 60 days.

(7)

Comprised of 737,894 shares of our common stock issuable upon exercise of a warrant issued by TOP to Mr. Taubenfeld, of which approximately 527,067 are exercisable as of January 8, 2019, at an exercise price of $0.66 per share.

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DESCRIPTION OF OUR CAPITAL STOCK

General

Prior to the Distribution, Alliqua, as our sole stockholder, will approve and adopt our Amended and Restated Certificate of Incorporation, and our Board of Directors will approve and adopt our Amended and Restated Bylaws. The following summarizes information concerning our capital stock, including material provisions of our Amended and Restated Certificate of Incorporation, our Amended and Restated Bylaws and certain provisions of Delaware law. You are encouraged to read our form of Amended and Restated Certificate of Incorporation and our form of Amended and Restated Bylaws, which are filed as exhibits to our Registration Statement on Form S-1, of which this prospectus is part, for greater detail with respect to these provisions.

Authorized Capital Stock

Immediately following the Spin-Off, our authorized capital stock will consist of 100,000,000 shares of common stock, par value $0.001 per share, and 5,000,000 shares of “blank check” preferred stock, par value $0.001 per share.

Shares Outstanding

Immediately following the Spin-Off, the Merger, and the transactions contemplated thereby, including the Private Placement, we estimate that approximately 17,204,000 shares of our common stock will be issued and outstanding, based on approximately 5,005,210 shares of Alliqua common stock outstanding as of December 31, 2018.

Common Stock

Dividend Rights

Subject to preferences that may be applicable to any then outstanding preferred stock, holders of our common stock are entitled to receive dividends, if any, as may be declared from time to time by our Board of Directors out of legally available funds. See “Dividend Policy.”

Voting Rights

Except as required by law or matters relating solely to the terms of preferred stock, each outstanding share of common stock will be entitled to one vote on all matters submitted to a vote of stockholders. Holders of shares of our common stock shall have no cumulative voting rights. Except in respect of matters relating to the election and removal of directors on our Board of Directors and as otherwise provided in our Amended and Restated Certificate of Incorporation or required by law, all matters to be voted on by our stockholders must be approved by a majority of the shares present in person or by proxy at the meeting and entitled to vote on the subject matter. In the case of election of directors, all matters to be voted on by our stockholders must be approved by a plurality of the voting power of the shares present in person or by proxy at the meeting and entitled to vote thereon.

Liquidation

In the event of the liquidation, dissolution or winding up of our company, holders of our common stock are entitled to share ratably in the net assets legally available for distribution to stockholders after the payment of all of our debts and other liabilities and the satisfaction of any liquidation preference granted to the holders of any then outstanding shares of preferred stock.

Rights and Preferences

Holders of our common stock have no preemptive, conversion, subscription or other rights, and there is no redemption or sinking fund provisions applicable to our common stock. The rights, preferences and privileges of the holders of our common stock are subject to, and may be adversely affected by, the rights of the holders of shares of any series of our preferred stock that we may designate in the future.

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Preferred Stock

The Board of Directors is authorized, subject to any limitations prescribed by law, without further vote or action by the shareholders, to issue from time to time shares of preferred stock in one or more series. Preferred stock may be convertible into shares of our common stock or other series of preferred stock. Each such series of preferred stock shall have such number of shares, designations, preferences, voting powers, qualifications, and special or relative rights or privileges as shall be determined by the Board of Directors, which may include, among others, dividend rights, voting rights, liquidation preferences, conversion rights and preemptive rights. Issuance of preferred stock by our Board of Directors may result in such shares having dividend or liquidation preferences senior to the rights of the holders of our common stock and could dilute the voting rights of the holders of our common stock.

Prior to the issuance of shares of each series of preferred stock, the Board of Directors is required by the Delaware General Corporation Law and our certificate of incorporation to adopt resolutions and file a certificate of designation with the Secretary of State of the State of Delaware. The certificate of designation fixes for each class or series the designations, powers, preferences, rights, qualifications, limitations and restrictions. Once designated by our Board of Directors, each series of preferred stock may have specific financial and other terms.

Delaware Anti-Takeover Law and Provisions of our Amended and Restated Certificate of Incorporation and Amended and Restated Bylaws

Delaware Anti-Takeover Law

We are subject to Section 203 of the Delaware General Corporation Law. Section 203 generally prohibits a public Delaware corporation from engaging in a “business combination” with an “interested stockholder” for a period of three years after the date of the transaction in which the person became an interested stockholder, unless:

•

prior to the date of the transaction, the board of directors of the corporation approved either the business combination or the transaction which resulted in the stockholder becoming an interested stockholder;

•

the interested stockholder owned at least 85% of the voting stock of the corporation outstanding at the time the transaction commenced, excluding for purposes of determining the number of shares outstanding (i) shares owned by persons who are directors and also officers and (ii) shares owned by employee stock plans in which employee participants do not have the right to determine confidentially whether shares held subject to the plan will be tendered in a tender or exchange offer; or

•

on or subsequent to the date of the transaction, the business combination is approved by the board and authorized at an annual or special meeting of stockholders, and not by written consent, by the affirmative vote of at least 662∕3% of the outstanding voting stock which is not owned by the interested stockholder.

Section 203 defines a business combination to include:

•

any merger or consolidation involving the corporation and the interested stockholder;

•

any sale, transfer, pledge or other disposition involving the interested stockholder of 10% or more of the assets of the corporation;

•

subject to exceptions, any transaction that results in the issuance or transfer by the corporation of any stock of the corporation to the interested stockholder;

•

subject to exceptions, any transaction involving the corporation or any direct or indirect majority-owned subsidiary of the corporation which has the effect, directly or indirectly, of increasing the proportionate share of the stock of any class or series, or securities convertible into the stock of any class or series, of the corporation or of any such subsidiary which is owned by the interested stockholder; or

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•

the receipt by the interested stockholder of the benefit of any loans, advances, guarantees, pledges or other financial benefits provided by or through the corporation.

In general, Section 203 defines an interested stockholder as any entity or person beneficially owning 15% or more of the outstanding voting stock of the corporation or any entity or person affiliated with, or controlling, or controlled by, the entity or person. The term “owner” is broadly defined to include any person that, individually, with or through that person’s affiliates or associates, among other things, beneficially owns the stock, or has the right to acquire the stock, whether or not the right is immediately exercisable, under any agreement or understanding or upon the exercise of warrants or options or otherwise or has the right to vote the stock under any agreement or understanding, or has an agreement or understanding with the beneficial owner of the stock for the purpose of acquiring, holding, voting or disposing of the stock.

The restrictions in Section 203 do not apply to corporations that have elected, in the manner provided in Section 203, not to be subject to Section 203 of the Delaware General Corporation Law or, with certain exceptions, which do not have a class of voting stock that is listed on a national securities exchange or authorized for quotation on the Nasdaq Stock Market or held of record by more than 2,000 stockholders. Our Amended and Restated Certificate of Incorporation and Bylaws do not opt out of Section 203.

Section 203 could delay or prohibit mergers or other takeover or change in control attempts with respect to us and, accordingly, may discourage attempts to acquire us even though such a transaction may offer our stockholders the opportunity to sell their stock at a price above the prevailing market price.

Certificate of Incorporation and Bylaws

Provisions of our Amended and Restated Certificate of Incorporation and Bylaws may delay or discourage transactions involving an actual or potential change in our control or change in our management, including transactions in which shareholders might otherwise receive a premium for their shares, or transactions that our shareholders might otherwise deem to be in their best interests. Therefore, these provisions could adversely affect the price of our common stock. Among other things, our Amended and Restated Certificate of Incorporation and Bylaws:

•

permit our board of directors to issue up to 5,000,000 shares of preferred stock, without further action by the shareholders, with any rights, preferences and privileges as they may designate, including the right to approve an acquisition or other change in control;

•

provide that the authorized number of directors may be changed only by resolution of a majority of the total number of authorized directors whether or not there exist any vacancies in the previously authorized directorships (the “Whole Board”);

•

provide that all vacancies, including newly created directorships, may, except as otherwise required by law, be filled by the affirmative vote of a majority of directors then in office, even if less than a quorum;

•

do not provide for cumulative voting rights (therefore allowing the holders of a majority of the shares of common stock entitled to vote in any election of directors to elect all of the directors standing for election, if they should so choose);

•

provide that special meetings of our shareholders may be called only by the the Board of Directors acting pursuant to a resolution adopted by a majority of the Whole Board or holders of a majority of the outstanding voting power of the shares of capital stock of the Company; and

•

set forth an advance notice procedure with regard to the nomination, other than by or at the direction of our board of directors, of candidates for election as directors and with regard to business to be brought before a meeting of shareholders.

Limitation on Liability and Indemnification of Directors and Executive Officers

Our Amended and Restated Certificate of Incorporation will limit our directors’ liability to the fullest extent permitted under Delaware law. Delaware law provides that directors of a corporation will not be personally liable for monetary damages for breach of their fiduciary duties as directors, except for liability:

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•

for any breach of a director’s duty of loyalty to us and our stockholders;

•

for any act or omission not in good faith or that involves intentional misconduct or a knowing violation of law;

•

under Section 174 of the Delaware General Corporation Law (unlawful payment of dividends or redemption of shares); or

•

for any breach of a director’s duty of loyalty to us or our stockholders.

If the Delaware General Corporation Law is amended to authorize corporate action further eliminating or limiting the personal liability of directors, then the liability of our directors shall be eliminated or limited to the fullest extent permitted by the Delaware General Corporation Law, as so amended.

Delaware law provides, and our Amended and Restated Bylaws will provide that we will, in certain situations, indemnify our directors and officers and may indemnify other employees and other agents, to the fullest extent permitted by law. Any indemnified person is also entitled, subject to certain limitations, to payment or reimbursement of reasonable expenses in advance of the final disposition of the proceeding.

We intend to maintain a directors’ and officers’ insurance policy pursuant to which our directors and officers are insured against liability for certain actions taken in their capacities as directors and officers. We believe that these provisions in our Amended and Restated Certificate of Incorporation and Bylaws and any such insurance policy are necessary to attract and retain qualified persons as directors and officers.

Insofar as indemnification for liabilities arising under the Securities Act, may be permitted to directors, officers or control persons, in the opinion of the SEC, such indemnification is against public policy as expressed in the Securities Act and is therefore unenforceable.

Authorized but Unissued Shares

Our authorized but unissued shares of common stock and preferred stock are available for future issuance without your approval. We may use additional shares for a variety of purposes, including future public offerings to raise additional capital, to fund acquisitions and as employee compensation. The existence of authorized but unissued shares of common stock and preferred stock could render more difficult or discourage an attempt to obtain control of us by means of a proxy contest, tender offer, merger or otherwise.

Choice of Forum

Our Amended and Restated Bylaws will provide that the sole and exclusive forum for (i) any derivative action or proceeding brought on our behalf; (ii) any action asserting a claim of breach of fiduciary duty owed by any director or officer or other employee to us or our stockholders; (iii) any action asserting a claim against us or any director or officer or other employee arising pursuant to any provision of the Delaware General Corporation Law, our Amended and Restated Certificate of Incorporation or our Amended and Restated Bylaws (in each case, as may be amended from time to time); (iv) any action asserting a claim against us or any director or officer or other employee of governed by the internal affairs doctrine; or (v) any other internal corporate claim as defined in Section 115 of the Delaware General Corporation Law or any successor provision, shall be in the Court of Chancery of the State of Delaware, or, if the Court of Chancery of the State of Delaware does not have jurisdiction, the Superior Court of the State of Delaware, or, if the Superior Court of the State of Delaware does not have jurisdiction, the United States District Court for the District of Delaware, subject to the court’s having personal jurisdiction over the indispensable parties named therein. The enforceability of similar choice of forum provisions in other companies’ certificates of incorporation has been challenged in legal proceedings, and it is possible that a court could rule that these types of provisions to be inapplicable or unenforceable.

Stock Exchange Listing

We intend to list our common stock on the Nasdaq Capital Market under the symbol “TOPP.”

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SHARES ELIGIBLE FOR FUTURE SALE

There is currently no public market for our common stock. Future sales of substantial amounts of our common stock in the public market, or the availability of such shares for sale in the public market, could adversely affect the market price of our common stock prevailing from time to time and could impair our ability to raise capital through sales of equity securities.

Sale of Restricted Securities

The shares of our common stock distributed to Alliqua stockholders will be freely transferable, except for shares received by individuals who are our affiliates. Individuals who may be considered our affiliates after the Spin-Off include individuals who control, are controlled by or are under common control with us, as those terms generally are interpreted for federal securities law purposes. These individuals may include some or all of our directors and executive officers. Individuals who are our affiliates will be permitted to sell their shares of our common stock only pursuant to an effective registration statement under the Securities Act, or an exemption from the registration requirements of the Securities Act, such as those afforded by Section 4(1) of the Securities Act or Rule 144 thereunder.

Rule 144

In general, under Rule 144 as currently in effect, a person (or persons whose shares are aggregated), including an affiliate, who beneficially owns “restricted securities” of a “reporting company” may not sell these securities until the person has beneficially owned them for at least six months. Thereafter, affiliates may not sell within any three-month period a number of shares in excess of the greater of: (i) 1% of the then outstanding shares of common stock as shown by the most recent report or statement published by the issuer; and (ii) the average weekly reported trading volume in such securities during the four preceding calendar weeks.

Sales under Rule 144 by our affiliates will also be subject to restrictions relating to manner of sale, notice and the availability of current public information about us and may be affected only through unsolicited brokers’ transactions.

Persons not deemed to be affiliates who have beneficially owned “restricted securities” for at least six months but for less than one year may sell these securities, provided that current public information about the Company is “available,” which means that, on the date of sale, we have been subject to the reporting requirements of the Exchange Act for at least 90 days and are current in our Exchange Act filings. After beneficially owning “restricted securities” for one year, our non-affiliates may engage in unlimited re-sales of such securities.

Shares received by our affiliates in the Distribution or upon exercise of stock options or upon vesting of other equity-linked awards may be “controlled securities” rather than “restricted securities.” “Controlled securities” are subject to the same volume limitations as “restricted securities” but are not subject to holding period requirements.

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LEGAL MATTERS

The validity of the common stock to be distributed in the Spin-Off will be passed upon for the Company by Haynes & Boone, LLP, New York, New York.

EXPERTS

The financial statements of each of AquaMed and TOP as of December 31, 2017 and 2016 and for each of the two years ended December 31, 2017 and 2016 included in this prospectus have been so included in reliance on the report of Marcum LLP, an independent registered public accounting firm, given on the authority of said firm as experts in auditing and accounting.

WHERE YOU CAN FIND MORE INFORMATION

We have filed a Registration Statement on Form S-1 with the SEC with respect to the shares of our common stock that Alliqua’s stockholders will receive in the Distribution as contemplated by this prospectus. This prospectus is a part of and does not contain all the information set forth in, the Registration Statement and the other exhibits and schedules to the Registration Statement. For further information with respect to us and our common stock, please refer to the Registration Statement including its other exhibits and schedules. Statements we make in this prospectus relating to any contract or other document are not necessarily complete and you should refer to the exhibits attached to the Registration Statement for copies of the actual contract or document. You may review a copy of the Registration Statement including its exhibits and schedules at the SEC’s public reference room, located at 100 F Street, N.E., Washington, D.C. 20549, as well as on the Internet website maintained by the SEC at www.sec.gov. Please call the SEC at 1-800-SEC-0330 for more information on the public reference room. Information contained on, or hyperlinked from, any website we refer to in this prospectus does not and will not constitute a part of this prospectus or the Registration Statement on Form S-1 of which this prospectus is a part.

As a result of the Spin-Off, we will become subject to the information and reporting requirements of the Exchange Act and, in accordance with the Exchange Act, we will file periodic reports, proxy statements and other information with the SEC.

You may request a copy of any of our filings with the SEC at no cost by writing us at the following address:

Before the Spin-Off, at:

Investor Relations
Alliqua BioMedical, Inc.
2150 Cabot Boulevard West
Suite B
Langhorne, PA 19047
Phone: 215-702-8550

After the Spin-Off, at:

Investor Relations
AquaMed Technologies, Inc.
2150 Cabot Boulevard West
Suite B
Langhorne, PA 19047
Phone: 215-702-8550

We intend to furnish holders of our common stock with annual reports containing combined financial statements prepared in accordance with U.S. generally accepted accounting principles and audited and reported on by an independent registered public accounting firm.

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REPORT OF INDEPENDENT REGISTERED PUBLIC ACCOUNTING FIRM

To the Shareholders and Board of Directors of
Alliqua BioMedical, Inc.

Opinion on the Financial Statements

We have audited the accompanying balance sheets of AquaMed Technologies, Inc. (a segment of Alliqua BioMedical, Inc.) (the “Company”), as of December 31, 2017 and 2016, the related statements of operations, parent’s net investment and cash flows for each of the two years in the period ended December 31, 2017, and the related notes (collectively referred to as the “financial statements”). In our opinion, the financial statements present fairly, in all material respects, the financial position of the Company as of December 31, 2017 and 2016, and the results of its operations and its cash flows for each of the two years in the period ended December 31, 2017, in conformity with accounting principles generally accepted in the United States of America

Explanatory Paragraph — Going Concern

The accompanying financial statements have been prepared assuming that the Company will continue as a going concern. As more fully described in Note 3, the Company has incurred significant losses and needs to raise additional funds to meet its obligations and sustain its operations. These conditions raise substantial doubt about the Company’s ability to continue as a going concern. Management’s plans in regard to these matters are also described in Note 3. The financial statements do not include any adjustments that might result from the outcome of this uncertainty.

Basis for Opinion

These financial statements are the responsibility of the Company’s management. Our responsibility is to express an opinion on the Company’s financial statements based on our audits. We are a public accounting firm registered with the Public Company Accounting Oversight Board (United States) (“PCAOB”) and are required to be independent with respect to the Company in accordance with the U.S. federal securities laws and the applicable rules and regulations of the Securities and Exchange Commission and the PCAOB.

We conducted our audits in accordance with the standards of the PCAOB. Those standards require that we plan and perform the audits to obtain reasonable assurance about whether the financial statements are free of material misstatement, whether due to error or fraud. The Company is not required to have, nor were we engaged to perform, an audit of its internal control over financial reporting. As part of our audits we are required to obtain an understanding of internal control over financial reporting but not for the purpose of expressing an opinion on the effectiveness of the Company’s internal control over financial reporting. Accordingly, we express no such opinion.

Our audits included performing procedures to assess the risks of material misstatement of the financial statements, whether due to error or fraud, and performing procedures that respond to those risks. Such procedures included examining, on a test basis, evidence regarding the amounts and disclosures in the financial statements. Our audits also included evaluating the accounting principles used and significant estimates made by management, as well as evaluating the overall presentation of the financial statements. We believe that our audits provide a reasonable basis for our opinion.

/s/ Marcum llp
Marcum llp

We have served as the Company’s auditor since 2010.

New York, NY
January 8, 2019

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AQUAMED TECHNOLOGIES, INC.
(A SEGEMENT OF ALLIQUA BIOMEDICAL, INC.)

STATEMENTS OF CASH FLOWS
(in thousands)

	Years Ended December 31,
	2017			2016
Operating Activities
Net loss		$	(953)		$	(1,776)
Adjustments to reconcile net loss to net cash used in operating activities:
Depreciation and amortization			316			324
Amortization of deferred lease incentive			(8)			(9)
Deferred income tax expense			(16)			(63)
Provision for doubtful accounts			2			12
Provision for excess and slow moving inventory			5			—
Changes in operating assets and liabilities:
Accounts receivable			(27)			212
Inventory			60			46
Prepaid expenses and other assets			18			15
Accounts payable			(84)			(35)
Accrued expenses and other liabilities			(90)			(43)
Net Cash Used in Operating Activities			(777)			(1,317)
Investing Activities
Purchase of improvements and equipment			(7)			—
Net Cash Used in Investing Activities			(7)			—
Financing Activities
Advances from parent			784			1,317
Net Cash Provided by Financing Activities			784			1,317
Net Increase (Decrease) in Cash and Cash Equivalents			—			—
Cash and Cash Equivalents – Beginning of year			—			—
Cash and Cash Equivalents – End of year		$	—		$	—
Supplemental Disclosure of Cash Flows Information
Cash paid during the period for:
Interest		$	—		$	—
Taxes			—			—

The accompanying notes are an integral part of these financial statements.

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AQUAMED TECHNOLOGIES, INC.
(A SEGMENT OF ALLIQUA BIOMEDICAL, INC.)

NOTES TO FINANCIAL STATEMENTS
FOR YEARS ENDED DECEMBER 31, 2017 AND 2016

Description of Business and Basis of Presentation

AquaMed Technologies, Inc. (“AquaMed” or the “Company”) manufactures high water content, electron beam cross-linked, aqueous polymer hydrogels, or gels, used for wound care, medical diagnostics, transdermal drug delivery and cosmetics. The Company believes that it is one of the leading manufacturers of high-performance gels in the United States. The Company specializes in custom gels by capitalizing on proprietary manufacturing technologies. The Company has, historically, served as a contract manufacturer, supplying its gels to third parties who incorporate them into their own products.

Recent Developments

On November 27, 2018, AquaMed, a wholly-owned subsidiary of Alliqua BioMedical, Inc. (“Alliqua” or the “Parent”), AQ TOP, LLC, a Delaware limited liability company and a wholly-owned subsidiary of AquaMed (“Merger Sub”), and TO Pharmaceuticals, LLC, a Delaware limited liability company (“TOP”), entered into an Agreement and Plan of Merger (the “Merger Agreement”), pursuant to which, among other things, subject to the satisfaction or waiver of the conditions set forth in the Merger Agreement, Merger Sub will merge with and into TOP, with TOP becoming a wholly-owned subsidiary of the AquaMed and the surviving company of the merger (the “Merger”). The Merger is intended to qualify for federal income tax purposes as a tax-free contribution under the provisions of Section 351(a) of the Internal Revenue Code of 1986, as amended.

The Merger will occur after the consummation by Alliqua of the following steps:

(1)

Pursuant to an Asset Contribution and Separation Agreement to be entered into by and between Alliqua and AquaMed (the “Separation Agreement”) prior to consummation of the Merger, Alliqua will transfer certain assets and liabilities utilized primarily in connection with its custom hydrogels contract manufacturing business to AquaMed (the “Separation”),

(2)

AquaMed will issue a to be determined number of shares of common stock to Alliqua in consideration of the contribution of assets pursuant to the Separation Agreement (the “Distribution Consideration”),

(3)

Alliqua will distribute to its stockholders all of the issued and outstanding shares of common stock, par value $0.001 per share, of AquaMed by way of a pro rata dividend (the “Distribution”), and

(4)

Alliqua will consummate the previously announced reverse merger transaction with Adynxx, Inc. (“Adynxx”), pursuant to that certain Agreement and Plan of Merger and Reorganization, dated as of October 11, 2018, by and among Alliqua, Embark Merger Sub, Inc. and Adynxx.

At the effective time of the Merger, all of the outstanding membership units of TOP will be converted into the right to receive, in the aggregate, merger consideration consisting of shares of AquaMed common stock. Immediately after the effective time of the Merger and consummation of the Private Placement (as defined below), before giving effect to any fees payable in equity to financial advisors or other intermediaries, the current members of TOP and the third-party investors that participate in the Private Placement are expected to hold approximately 90% of the total number of shares of AquaMed common stock outstanding (on a fully diluted basis).

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AQUAMED TECHNOLOGIES, INC.
(A SEGMENT OF ALLIQUA BIOMEDICAL, INC.)

NOTES TO FINANCIAL STATEMENTS
FOR YEARS ENDED DECEMBER 31, 2017 AND 2016

Description of Business and Basis of Presentation – (continued)

effective time of the Merger (the “Private Placement”) (iv) the accuracy of the parties’ representations and warranties and the performance of their respective covenants contained in the Merger Agreement, and (v) receipt of an independent third-party valuation of the AquaMed common stock to be issued in the Distribution.

The Merger Agreement contains customary and other representations, warranties and covenants, including a covenant for AquaMed to use (i) commercially reasonable efforts to consummate and make effective the Separation and payment of the Distribution Consideration contemplated by the Distribution Agreement in accordance with its terms and (ii) reasonable best efforts to consummate the Private Placement.

Basis of Presentation

The Company is being presented as a carve out of the Contract Manufacturing segment of Alliqua, which includes AquaMed and certain other accounts of Alliqua and collectively presents the Company on a standalone basis.

Management believes the assumptions underlying the Company’s standalone financial statements are reasonable. Nevertheless, the financial statements may not include all of the actual expenses that would have been incurred had the Company operated as a standalone company during the periods presented, and may not reflect the Company’s results of operations, financial position and cash flows had the Company operated as a standalone company during the periods presented. Actual costs that would have been incurred if the Company had operated as a standalone company would depend on multiple factors, including organizational structure and strategic decisions made in various areas.

Alliqua used a centralized approach to cash management and financing its operations, including the operations of the Company. Accordingly, none of the cash and cash equivalents of Alliqua have been allocated to the Company in the financial statements. Transactions between Alliqua and the Company are accounted for through Parent’s Net Investment.

Significant Accounting Policies and Estimates

Use of Estimates in the Financial Statements

The preparation of the financial statements in conformity with generally accepted accounting principles requires management to make estimates and assumptions that affect the amounts reported in the financial statements and accompanying notes. These estimates and assumptions include valuing the allowance for doubtful accounts, inventory reserves, deferred taxes and related valuation allowances, and the fair values of long-lived assets. Actual results could differ from the estimates.

Trade Accounts Receivable

Trade accounts receivable are stated at the amount the Company expects to collect and do not bear interest. The Company evaluates the collectability of accounts receivable based on a combination of factors. In circumstances where a specific customer is unable to meet its financial obligations to the Company, a provision to the allowances for doubtful accounts is recorded against amounts due to reduce the net recognized receivable to the amount that is reasonably expected to be collected. For all other customers, a provision to the allowances for doubtful accounts is recorded based on factors including the length of time the receivables are past due, the current business environment and the Company’s historical experience. Provisions to the allowances for doubtful accounts are recorded to selling, general and administrative expenses. Account balances are charged off against the allowance when it is probable that the receivable will not be recovered. The allowance for doubtful accounts was $2,000 as of December 31, 2017 and $14,000 as of December 31, 2016.

F-8

TABLE OF CONTENTS

AQUAMED TECHNOLOGIES, INC.
(A SEGMENT OF ALLIQUA BIOMEDICAL, INC.)

NOTES TO FINANCIAL STATEMENTS
FOR YEARS ENDED DECEMBER 31, 2017 AND 2016

Description of Business and Basis of Presentation – (continued)

Inventory

Inventory is stated at the lower of cost, the value determined by the first-in, first-out method, or net realizable value. At each balance sheet date, the Company evaluates inventories for excess quantities, obsolescence or shelf life expiration. This evaluation includes analysis of historical sales levels by product, projections of future demand, the risk of technological or competitive obsolescence for products, general market conditions, and a review of the shelf life expiration dates for products. To the extent that management determines there are excess or obsolete inventory or quantities with a shelf life that is too near its expiration for the Company to reasonably expect that it can sell those products prior to their expiration, the Company adjusts the carrying value to estimated net realizable value.

Improvements and Equipment

Improvements and equipment are recorded at cost. Depreciation of equipment is computed utilizing the straight-line method over the estimated useful lives of the assets. Amortization of leasehold improvements is computed utilizing the straight-line method over the lesser of the lease term or the estimated useful life. Repairs and maintenance costs are expensed as incurred. The cost of major additions and improvements is capitalized, while maintenance and repair costs that do not improve or extend the lives of the respective assets are charged to operations as incurred.

Revenue Recognition

Revenue is recognized when persuasive evidence of an arrangement exists, delivery has occurred, title and risk of loss have passed to the customer, there is a fixed or determinable sales price, and collectability of that sales price is reasonably assured.

Cost of Goods Sold and Selling, General and Administrative Expenses

Costs associated with the production and procurement of product are included in cost of goods sold, including shipping and handling costs such as inbound freight costs, purchasing and receiving costs, inspection costs and other product procurement related charges. All other expenses are included in selling, general and administrative expenses, as the predominant expenses associated therewith are general and administrative in nature.

Shipping and Handling

Amounts billed to customers for shipping and handling are included in revenues. The related shipping and freight charges incurred by the Company are included in cost of goods sold and were not material for either the years ended December 31, 2017 or 2016.

Income Taxes

Income taxes are accounted for under the asset and liability method as if the Company were a separate taxpayer during the period that its operations were included as part of a federal consolidated tax return filing group with its parent company. Under this method, deferred tax assets and liabilities are recognized for the expected future tax consequences attributable to temporary differences between the financial statement carrying amounts and their respective tax bases of assets and liabilities and the expected benefits of net operating loss and credit carryforwards. Deferred tax assets and liabilities are measured using enacted tax rates expected to apply to taxable income in the years in which those temporary differences are expected to be recovered or settled. The effect on deferred tax assets and liabilities of a change in tax rates is recognized in operations in the period enacted. A valuation allowance is provided when it is more likely

F-9

TABLE OF CONTENTS

AQUAMED TECHNOLOGIES, INC.
(A SEGMENT OF ALLIQUA BIOMEDICAL, INC.)

NOTES TO FINANCIAL STATEMENTS
FOR YEARS ENDED DECEMBER 31, 2017 AND 2016

Description of Business and Basis of Presentation – (continued)

than not that a portion or all of a deferred tax asset will not be realized. The ultimate realization of deferred tax assets is dependent upon the generation of future taxable income and the reversal of deferred tax liabilities during the period in which related temporary differences become deductible.

The Company adopted the provisions of Accounting Standards Codification Topic 740 (“ASC 740”) related to the accounting for uncertainty in income taxes recognized in an enterprise’s consolidated financial statements. ASC 740 prescribes a comprehensive model for the financial statement recognition, measurement, presentation and disclosure of uncertain tax positions taken or expected to be taken in income tax returns.

The benefit of tax positions taken or expected to be taken in the Company’s income tax returns are recognized in the financial statements if such positions are more likely than not of being sustained upon examination by taxing authorities. Differences between tax positions taken or expected to be taken in a tax return and the benefit recognized and measured pursuant to the interpretation are referred to as “unrecognized benefits”. A liability is recognized (or amount of net operating loss carryover or amount of tax refundable is reduced) for an unrecognized tax benefit because it represents an enterprise’s potential future obligation to the taxing authority for a tax position that was not recognized as a result of applying the provisions of ASC 740. Interest costs and related penalties related to unrecognized tax benefits are required to be calculated, if applicable. The Company’s policy is to classify assessments, if any, for tax related interest as interest expense and penalties as selling, general and administrative expenses. No interest or penalties were recorded during the years ended December 31, 2017 and 2016. As of December 31, 2017, and December 31, 2016, no liability for unrecognized tax benefits was required to be reported. The Company does not expect any significant changes in its unrecognized tax benefits in the next year.

Under the separate entity method, the Company is assumed to file a separate return with the taxing authority, thereby reporting its taxable income or loss and paying the applicable tax to or receiving the appropriate refund from its parent. However, since there is no tax-sharing agreement in place between the Company and its parent, any taxes payable or receivable on current taxable income or loss at the end of each reporting date is treated as a capital contribution or dividend.

Parent’s Net Investment

The Company’s equity on the Balance Sheet represents Alliqua’s net investment in the Company’s business and is presented as “Parent’s Net Investment” in lieu of stockholder’s equity. The Statement of Changes in Parent’s Net Investment includes net cash transfers between Alliqua and the Company. Alliqua performs cash management and other treasury-related functions on a centralized basis for all of its divisions, which includes the Company. Liabilities recorded by Alliqua, whose related expenses have been pushed down to the Company, are included in the Parent’s Net Investment.

All transactions reflected in the Parent’s Net Investment in the accompanying Balance Sheets have been considered cash receipts and payments for purposes of the Statements of Cash Flows and are reflected in the financing activities in the accompanying Statements of Cash Flows.

Earnings per share data has not been presented in the accompanying Financial Statements because the Company did not operate as a separate legal entity with its own capital structure during the periods presented.

Subsequent Events

The Company evaluates events and/or transactions occurring after the balance sheet date and before the issue date of the carve-out financial statements to determine if any of those events and/or transactions requires adjustment to or disclosure in the carve-out financial statements.

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TABLE OF CONTENTS

AQUAMED TECHNOLOGIES, INC.
(A SEGMENT OF ALLIQUA BIOMEDICAL, INC.)

NOTES TO FINANCIAL STATEMENTS
FOR YEARS ENDED DECEMBER 31, 2017 AND 2016

Description of Business and Basis of Presentation – (continued)

Recent Accounting Principles

In August 2018, the FASB issued ASU 2018-13, “Fair Value Measurement (Topic 820): Disclosure Framework — Changes to the Disclosure Requirements for Fair Value Measurement”. The amendments in this update is to improve the effectiveness of disclosures in the notes to the financial statements by facilitating clear communication of the information required by GAAP that is most important to users of each entity’s financial statements. The amendments in this update apply to all entities that are required, under existing GAAP, to make disclosures about recurring or nonrecurring fair value measurements. The amendments in this update are effective for all entities for fiscal years beginning after December 15, 2019, and interim periods within those fiscal years. The Company does not expect that this guidance will have a material impact on its consolidated financial statements.

In July 2018, the FASB issued ASU 2018-11, “Leases (Topic 842): Target Improvements”. The amendments in this Update also clarify which Topic (Topic 842 or Topic 606) applies for the combined component. Specifically, if the non-lease component or components associated with the lease component are the predominant component of the combined component, an entity should account for the combined component in accordance with Topic 606. Otherwise, the entity should account for the combined component as an operating lease in accordance with Topic 842. An entity that elects the lessor practical expedient also should provide certain disclosures. The Company is currently evaluating the adoption of this guidance and does not expect that this guidance will have a material impact on its consolidated financial statements. The Company has not adopted this Standard and will do so at the effective date.

In July 2018, the FASB issued ASU 2018-10, “Codification Improvements to Topic 842, Leases”. The amendments in this Update affect narrow aspects of the guidance issued in the amendments in Update 2016-02 as described in the table below. The amendments in this update related to transition do not include amendments from proposed Accounting Standards Update, Leases (Topic 842): Targeted Improvements, specific to a new and optional transition method to adopt the new lease requirements in Update 2016-02. That additional transition method will be issued as part of a forthcoming and separate Update that will result in additional amendments to transition paragraphs included in this update to conform with the additional transition method. The Company is currently evaluating the adoption of this guidance and does not expect that this guidance will have a material impact on its consolidated financial statements. The Company has not adopted this Standard and will do so when specified by the FASB.

In June 2018, the FASB issued ASU 2018-07, “Compensation — Stock Compensation (Topic 718): Improvements to Nonemployee Share-Based Payment Accounting”. The amendments in this update is to maintain or improve the usefulness of the information provided to the users of financial statements while reducing cost and complexity in financial reporting. The areas for simplification in this Update involve several aspects of the accounting for nonemployee share-based payment transactions resulting from expanding the scope of Topic 718, to include share-based payment transactions for acquiring goods and services from nonemployees. Some of the areas for simplification apply only to nonpublic entities. The amendments in this update are effective for all entities for fiscal years beginning after December 15, 2018, and interim periods within those fiscal years. The Company does not expect that this guidance will have a material impact on its consolidated financial statements.

F-11

TABLE OF CONTENTS

AQUAMED TECHNOLOGIES, INC.
(A SEGMENT OF ALLIQUA BIOMEDICAL, INC.)

NOTES TO FINANCIAL STATEMENTS
FOR YEARS ENDED DECEMBER 31, 2017 AND 2016

Description of Business and Basis of Presentation – (continued)

measurement period beginning in the reporting period that includes the Act’s enactment date and ending when the Company has obtained, prepared, and analyzed the information needed in order to complete the accounting requirements but in no circumstances should the measurement period extend beyond one year from the enactment date. The Company has evaluated the Act and, based on the information available, recorded provisional amounts as the impacts can be reasonably estimated. These impacts are disclosed in “Note 8 — Income Taxes” in the Notes accompanying the audited Financial Statements.

In February 2016, the FASB issued Accounting Standards Update 2016-02, “Leases (Topic 842)” (“ASU 2016-02”). The standard requires a lessee to recognize assets and liabilities on the balance sheet for leases with lease terms greater than 12 months. The standard is effective for annual reporting periods beginning after December 15, 2018, which for the Company will commence with the year beginning January 1, 2019, with early application permitted. The adoption will require a modified retrospective approach for leases that exist or are entered into after the beginning of the earliest period presented. The Company is currently evaluating the standard to determine the impact of the adoption on the consolidated financial statements.

In November 2015, the FASB issued Accounting Standards Update 2015-17, “Income Taxes (Topic 740): Balance Sheet Classification of Deferred Taxes” (“ASU 2015-07”), an update to accounting guidance to simplify the presentation of deferred income taxes. The guidance requires an entity to classify all deferred tax liabilities and assets, along with any valuation allowance, as noncurrent in the balance sheet. The guidance is effective for public companies with annual reporting periods beginning after December 15, 2016, including interim periods within that reporting period. Early application is permitted. The Company has elected to early adopt ASU 2015-17 during the year ended December 31, 2015 with retrospective application. The adoption of ASU 2015-17 did not have a material impact on the Company’s consolidated financial statements.

In May 2014 the FASB issued Accounting Standards Update (ASU) No. 2014-09, Revenue from Contracts with Customers (Topic 606), which supersedes all existing revenue recognition requirements, including most industry-specific guidance. This new standard requires a company to recognize revenue when it transfers goods or services to customers in an amount that reflects the consideration that the company expects to receive for those goods or services. The FASB subsequently issued amendments to ASU No. 2014-09 that have the same effective date and transition date. These new standards became effective for us on January 1, 2018 and will be adopted using the modified retrospective method through a cumulative-effect adjustment, if any, directly to retained earnings as of that date. The Company has performed a review of these new standards as compared to our current accounting policies for its contract manufacturing revenues. As of December 31, 2017, the Company has not identified any accounting changes that would materially impact the amount of reported revenues with respect to our contract manufacturing revenues.

Carve-Out Assumptions and Allocations

The expenses of AquaMed for the years ended December 31, 2017 and 2016, including executive compensation, have been allocated by management between AquaMed and Alliqua, based either on specific attribution of those expenses or, where necessary and appropriate, based on management’s best estimate of an appropriate proportional allocation.

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TABLE OF CONTENTS

AQUAMED TECHNOLOGIES, INC.
(A SEGMENT OF ALLIQUA BIOMEDICAL, INC.)

NOTES TO FINANCIAL STATEMENTS
FOR YEARS ENDED DECEMBER 31, 2017 AND 2016

Carve-Out Assumptions and Allocations – (continued)

The following expenses included in the accounting records of AquaMed have been attributed by management to the operations being retained by AquaMed, accordingly:

	Year Ended December 31,
	2017			2016
Selling, general and administrative expenses
Compensation and benefits		$	184		$	269
Stock-based compensation			198			563
Other expenses and professional fees			734			918
Total selling, general and administrative expenses		$	1,116		$	1,750

Going Concern

The Company’s financial statements are prepared using accounting principles generally accepted in the United States of America applicable to a going concern that contemplates the realization of assets and liquidation of liabilities in the normal course of business.

The Company has experienced recurring losses since its merger with Alliqua BioMedical, Inc. in 2010. As of December 31, 2017, the Company had a $0 cash balance. For the years ended December 31, 2017 and 2016, the Company incurred net losses of $1.0 million and $1.8 million, respectively. These factors raise substantial doubt as to the Company’s ability to continue as a going concern within one year from the date these financial statements are issued.

The Company expects to continue incurring losses for the foreseeable future and will need to raise additional capital to support ongoing operations.

Inventory

Inventory consists of the following (in thousands):

	December 31, 2017			December 31, 2016
Raw materials		$	98		$	135
Work in process			—			21
Finished goods			—			2
Less: Inventory reserve for excess and slow moving inventory			(5)			—
Total		$	93		$	158

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TABLE OF CONTENTS

AQUAMED TECHNOLOGIES, INC.
(A SEGMENT OF ALLIQUA BIOMEDICAL, INC.)

NOTES TO FINANCIAL STATEMENTS
FOR YEARS ENDED DECEMBER 31, 2017 AND 2016

Accrued Expenses and Other Current Liabilities

Accrued expenses and other current liabilities consist of the following (in thousands):

	December 31, 2017			December 31, 2016
Salaries, benefits and incentive compensation		$	92		$	111
Professional fees			28			60
Other			27			66
Total accrued expenses and other current liabilities		$	147		$	237

Operating Leases

The Company leases one commercial manufacturing facility through an operating lease agreement for this facility located in Langhorne, Pennsylvania, through 2026. Tenant improvements are included in leasehold improvements on the balance sheet.

Future minimum lease payments, excluding expense reimbursements, under noncancelable operating leases at December 31, 2017 are as follows (in thousands):

2018		207
2019		207
2020		207
2021		207
2022		207
Thereafter		639
Total	$	1,674

Concentration of Risk

Revenue for the years ended December 31, 2017 and 2016, and accounts receivable as of December 31, 2017 from the Company’s largest customers, were as follows:

	% of Total Revenue				Accounts Receivable December 31, 2017
Customer	2017		2016		Accounts Receivable December 31, 2017
A		65%		72%		100%
B		16%		12%		0%

Improvements and Equipment, net

Improvements and equipment consist of the following (in thousands):

	Useful Life (Years)	December 31,
	Useful Life (Years)	2017			2016
Machinery and equipment	3 – 10		$	2,893		$	2,893
Office furniture and equipment	3 – 10			56			49
Leasehold improvements	(A)			228			228
				3,177			3,170
Less: Accumulated depreciation and amortization				(2,655)			(2,339)
Improvements and equipment, net			$	522		$	831

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TABLE OF CONTENTS

AQUAMED TECHNOLOGIES, INC.
(A SEGMENT OF ALLIQUA BIOMEDICAL, INC.)

NOTES TO FINANCIAL STATEMENTS
FOR YEARS ENDED DECEMBER 31, 2017 AND 2016

Improvements and Equipment, net – (continued)

(A)

Leasehold improvements are amortized over the shorter of the remaining lease term or estimated useful life.

Depreciation and Amortization expense was $316,000 and $324,000 for the years ended December 31, 2017 and 2016, respectively.

Income Taxes

These carve out financial statements are included in Alliqua’s Consolidated U.S. Federal return, while AquaMed files on a standalone basis in some state and local jurisdictions, including Pennsylvania, and has tax returns subject to examination by tax authorities generally beginning in the year ended December 31, 2014 and through December 31, 2017. However, to the extent we utilize our net operating loss (“NOL”) carryforwards in the future, the tax years in which the attribute was generated may still be adjusted upon examination by the Internal Revenue Service or state tax authorities of the future period tax return in which the attribute is utilized.

The income tax (benefit) provision consists of the following:

	For The Years Ended December 31,
	2017			2016
Federal:
Current		$	—		$	—
Deferred			(13)			(50)
State and local:
Current			—			—
Deferred			(3)			(13)
Income tax (benefit) provision		$	(16)		$	(63)

For the years ended December 31, 2017 and 2016, the expected tax benefit based on the statutory rate reconciled with the actual benefit is as follows:

	For The Years Ended December 31,
	2017		2016
U.S. federal statutory rate		34.0%		34.0%
State tax rate, net of federal benefit		0.1%		0.2%
Permanent differences – Other		0.0%		(0.3)%
Tax Reform – Federal Rate Change		(139.0)%		0.0%
Tax Reform – Change in valuation allowance		139.0%		0.0%
Change in valuation allowance		(32.4)%		(30.4)%
Income tax benefit		1.7%		3.5%

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TABLE OF CONTENTS

AQUAMED TECHNOLOGIES, INC.
(A SEGMENT OF ALLIQUA BIOMEDICAL, INC.)

NOTES TO FINANCIAL STATEMENTS
FOR YEARS ENDED DECEMBER 31, 2017 AND 2016

Income Taxes – (continued)

On December 22, 2017 the U.S. government enacted significant changes to federal tax law following the passage of the Tax Cuts and Jobs Act (“the Act”). The Act significantly changes the U.S. corporate tax system. The Company has reasonably estimated the accounting for the effects of the Act during the year ended December 31, 2017. Our financial statements for the year ended December 31, 2017 reflect certain effects of the Act including a reduction in the corporate tax rate from 34% to 21%. As we have recorded a full valuation allowance against our net deferred tax assets as of December 31, 2017, these changes have no impact on the income tax benefit for year ended December 31, 2017. We have recorded changes to our deferred tax assets and liabilities due to enactment of the Act. As a result of the change in U.S. corporate income tax rate, the Company recorded a decrease in our net deferred tax asset of approximately $1.3 million, which was offset by a decrease in valuation allowance. Given the significant changes resulting from and complexities associated with the Act, the financial impacts for the fourth quarter and full year 2017 are provisional and subject to further analysis, interpretation and clarification of the Act, which could result in changes to these estimates during 2018. During the quarter ended September 30, 2018, the Company finalized its U.S. federal 2017 income tax return, which resulted in an immaterial change in the net deferred tax asset, before valuation allowance, as of the enactment date. The Company has not adjusted the provisional estimates recorded during period ended December 31, 2017 under SAB 118 and will complete the accounting for the income tax effects of the Act prior to the end of the one-year measurement period.

As of December 31, 2017 and 2016, the Company’s deferred tax assets consisted of the effects of temporary differences attributable to the following:

	As of December 31,
	2017			2016
Deferred tax assets:
Net operating loss carryforwards		$	2,752		$	3,823
Intangible Assets			233			415
Goodwill and Tradename			29			—
Accruals			21			51
Other			2			5
Total deferred tax assets			3,037			4,294
Valuation allowance			(2,957)			(4,027)
Deferred tax assets, net of valuation allowance		$	80		$	267
Deferred tax liabilities:
Property and equipment			(80)			(267)
Intangible assets			—			—
Goodwill and Trade Name			—			(16)
Total deferred tax liabilities			(80)			(283)
Net deferred tax liabilities		$	—		$	(16)

The deferred tax assets associated with net operating losses included in the table above reflect proforma net operating losses as if the Company were a separate taxpayer during the periods presented. The corporate income tax returns of AquaMed, for the years ended December 31, 2017 and 2016, reported approximately $10.2 million and $9.7 million of federal NOL carryovers, respectively, which substantially begin to expire in 2028 and through 2035. Similarly, the subsidiary’s Pennsylvania state returns reported

F-16

TABLE OF CONTENTS

AQUAMED TECHNOLOGIES, INC.
(A SEGMENT OF ALLIQUA BIOMEDICAL, INC.)

NOTES TO FINANCIAL STATEMENTS
FOR YEARS ENDED DECEMBER 31, 2017 AND 2016

Income Taxes – (continued)

state NOL carryovers of approximately $7.7 million and $7.7 million, as of December 31, 2017 and December 31, 2016, respectively. However, these loss carryforwards on a separate company basis may be subject to limitations on the amounts that may be utilized pursuant to Internal Revenue Code section 382 and applicable state law. The Company will need to determine the amounts that may be utilized on a separate company basis in the future as necessary.

In assessing the realization of deferred tax assets, management considers whether it is more likely than not that some portion or all of the deferred tax assets will be realized. The ultimate realization of the deferred tax assets is dependent upon the future generation of taxable income during the periods in which those temporary differences become deductible. Management considers the scheduled reversal of deferred tax liabilities, projected future taxable income and tax planning strategies in making this assessment. The deferred tax liabilities related to goodwill cannot be used in this determination since goodwill assets are considered to be assets with an indefinite life for financial reporting purposes. After consideration of all the evidence, both positive and negative, management has recorded a full valuation allowance against net deferred tax assets at December 31, 2017 and December 31, 2016 because management has determined that it is more likely than not that these deferred tax assets will not be realized. The valuation allowance decreased by $1.1 million and increased by $0.6 million during the years ended December 31, 2017 and December 31, 2016, respectively. The decrease in tax year ended December 31, 2017 is primarily related to the decrease in the corporate tax rate from 34% to 21% due to the enactment of the Act. The increase in tax year ended December 31, 2016 is primarily related to changes to book-tax basis differences in fixed assets and intangible assets.

10.

Subsequent Event

On November 27, 2018, AquaMed Technologies, Inc. (“AquaMed”), a wholly-owned subsidiary of Alliqua, AQ TOP, LLC, a Delaware limited liability company and a wholly-owned subsidiary of AquaMed (“Merger Sub”), and TO Pharmaceuticals, LLC, a Delaware limited liability company (“TOP”), entered into an Agreement and Plan of Merger (the “Merger Agreement”), pursuant to which, among other things, subject to the satisfaction or waiver of the conditions set forth in the Merger Agreement, Merger Sub will merge with and into TOP, with TOP becoming a wholly-owned subsidiary of the AquaMed and the surviving company of the merger (the “Merger”) See Note 1 — Recent Developments.

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TABLE OF CONTENTS

AQUAMED TECHNOLOGIES, INC.
(A SEGMENT OF ALLIQUA BIOMEDICAL, INC.)

CONDENSED STATEMENTS OF CASH FLOWS
(Unaudited)
(in thousands)

	Nine Months Ended September 30,
	2018			2017
Operating Activities
Net loss		$	(1,323)		$	(759)
Adjustments to reconcile net loss to net cash used in operating activities:
Depreciation and amortization			243			237
Amortization of deferred lease incentive			(6)			(6)
Deferred income tax expense			—			(12)
Provision for doubtful accounts			2			(12)
Provision for excess and slow moving inventory			(5)			(5)
Changes in operating assets and liabilities:
Accounts receivable			(75)			(160)
Inventory			(85)			(8)
Prepaid expenses and other assets			(334)			16
Accounts payable			242			(39)
Accrued expenses and other liabilities			104			(99)
Net Cash Used in Operating Activities			(1,237)			(847)
Investing Activities
Purchase of improvements and equipment			—			(7)
Net Cash Used in Investing Activities			—			(7)
Financing Activities
Advances from parent			1,237			854
Net Cash Provided by Financing Activities			1,237			854
Net Increase (Decrease) in Cash and Cash Equivalents			—			—
Cash and Cash Equivalents – Beginning of period			—			—
Cash and Cash Equivalents – End of period		$	—		$	—
Supplemental Disclosure of Cash Flows Information
Cash paid during the period for:
Interest		$	—		$	—
Taxes			—			—

The accompanying notes are an integral part of these financial statements.

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TABLE OF CONTENTS

AQUAMED TECHNOLOGIES, INC.
(A SEGMENT OF ALLIQUA BIOMEDICAL, INC.)

NOTES TO CONDENSED UNAUDITED FINANCIAL STATEMENTS
FOR THE NINE MONTHS ENDED SEPTEMBER 30, 2018 AND 2017

Description of Business and Basis of Presentation

Aquamed Technologies, Inc. (“AquaMed” or the “Company”) manufactures high water content, electron beam cross-linked, aqueous polymer hydrogels, or gels, used for wound care, medical diagnostics, transdermal drug delivery and cosmetics. The Company believes that it is one of the leading manufacturers of high-performance gels in the United States. The Company specializes in custom gels by capitalizing on proprietary manufacturing technologies. The Company has, historically, served as a contract manufacturer, supplying its gels to third parties who incorporate them into their own products.

Recent Developments

The Merger will occur after the consummation by Alliqua of the following steps:

(1)

(2)

(3)

(4)

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TABLE OF CONTENTS

AQUAMED TECHNOLOGIES, INC.
(A SEGMENT OF ALLIQUA BIOMEDICAL, INC.)

NOTES TO CONDENSED UNAUDITED FINANCIAL STATEMENTS
FOR THE NINE MONTHS ENDED SEPTEMBER 30, 2018 AND 2017

Description of Business and Basis of Presentation – (continued)

Basis of Presentation

The accompanying unaudited condensed financial statements of the Company have been prepared in accordance with generally accepted accounting principles (“GAAP”) for interim financial information, which are the accounting principles that are generally accepted in the United States of America. Accordingly, they do not include all of the information and footnotes required by GAAP for complete financial statements. In the opinion of management, all adjustments (consisting of normal recurring accruals) considered necessary for a fair presentation have been included. These interim unaudited condensed financial statements should be read in conjunction with the Company’s audited financial statements and notes for the years ended December 31, 2017 and 2016 included elsewhere herein.

Significant Accounting Policies and Estimates

Use of Estimates in the Financial Statements

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TABLE OF CONTENTS

AQUAMED TECHNOLOGIES, INC.
(A SEGMENT OF ALLIQUA BIOMEDICAL, INC.)

NOTES TO CONDENSED UNAUDITED FINANCIAL STATEMENTS
FOR THE NINE MONTHS ENDED SEPTEMBER 30, 2018 AND 2017

Description of Business and Basis of Presentation – (continued)

Trade Accounts Receivable

Trade accounts receivable are stated at the amount the Company expects to collect and do not bear interest. The Company evaluates the collectability of accounts receivable based on a combination of factors. In circumstances where a specific customer is unable to meet its financial obligations to the Company, a provision to the allowances for doubtful accounts is recorded against amounts due to reduce the net recognized receivable to the amount that is reasonably expected to be collected. For all other customers, a provision to the allowances for doubtful accounts is recorded based on factors including the length of time the receivables are past due, the current business environment and the Company’s historical experience. Provisions to the allowances for doubtful accounts are recorded to selling, general and administrative expenses. Account balances are charged off against the allowance when it is probable that the receivable will not be recovered. The allowance for doubtful accounts was $3,500 as of September 30, 2018 and $2,000 as of December 31, 2017.

Inventory

Income Taxes

In accordance with ASC 740-270, Income Taxes — Interim Reporting, the Company is required at the end of each interim period to determine the best estimate of its annual effective tax rate and apply that rate to year-to-date ordinary income or loss. The resulting tax expense (or benefit) is adjusted for the tax effect of specific events, if any, required to be discretely recognized in the interim period as they occur. For the nine months ended September 30, 2018 and 2017, the Company recorded tax expense of none and $12,000, respectively. The Company has not recorded net deferred tax assets as of September 30, 2018 or December 31, 2017 because it maintained a full valuation allowance against all material deferred tax assets, and management has determined that it is more likely than not that the Company will be unable to realize those future benefits. The Company’s effective tax rate differs from the statutory rates of 21% and 34% as of September 30, 2018 and 2017, respectively, primarily attributable to losses for which no benefit is recognized. As of September 30, 2018, and December 31, 2017, the Company had no uncertain tax positions recorded in its balance sheets.

The United States enacted the Tax Cuts and Jobs Act (“Act”) on December 22, 2017, most provisions of which took effect in years beginning after December 31, 2017. The Act made substantial changes to U.S. taxation of corporations, including a reduction in the U.S. federal corporate income tax rate from 34% to 21%. The effect on deferred tax assets and liabilities of a change in law or tax rates is recognized in income in the period that includes the enactment date.

After the enactment of the Act, the SEC issued Staff Accounting Bulletin No. 118 (“SAB 118”) to address the application of U.S. GAAP in situations when a registrant does not have the necessary information available, prepared, or analyzed (including computations) in reasonable detail to complete the accounting for certain income tax effects of the Act. In our financial statements for the period ended December 31, 2017, we calculated an estimate of the impact of the Act related to the remeasurement of our

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AQUAMED TECHNOLOGIES, INC.
(A SEGMENT OF ALLIQUA BIOMEDICAL, INC.)

NOTES TO CONDENSED UNAUDITED FINANCIAL STATEMENTS
FOR THE NINE MONTHS ENDED SEPTEMBER 30, 2018 AND 2017

Description of Business and Basis of Presentation – (continued)

net U.S. deferred tax asset due to the change in U.S. federal corporate income tax rate. The provisional amount recorded was deferred tax expense of $1.3 million, but which was fully and equally offset by a deferred tax benefit related to a corresponding reduction in the Company’s valuation allowance. During the quarter ended September 30, 2018, the Company finalized its U.S. federal 2017 income tax return, which resulted in an immaterial change in the net deferred tax asset, before valuation allowance, as of the enactment date.

Parent’s Net Investment

The Company’s equity on the Balance Sheet represents Alliqua’s net investment in the Company’s business and is presented as “Net Parent’s Investment” in lieu of stockholder’s equity. The Statement of Changes in Parent’s Net Investment includes net cash transfers between Alliqua and the Company. Alliqua performs cash management and other treasury-related functions on a centralized basis for all of its divisions, which includes only the Company as of September 30, 2018. Liabilities recorded by Alliqua, whose related expenses have been pushed down to the Company, are included in the Parent’s Net Investment.

All transactions reflected in the Parent Net Investment in the accompanying Balance Sheets have been considered cash receipts and payments for purposes of the Statements of Cash Flows and are reflected in the financing activities in the accompanying Statements of Cash Flows.

Subsequent Events

Carve-Out Assumptions and Allocations

The expenses of AquaMed for the nine months ended September 30, 2018 and 2017, including executive compensation, have been allocated by management between AquaMed and Alliqua, based either on specific attribution of those expenses or, where necessary and appropriate, based on management’s best estimate of an appropriate proportional allocation.

The following expenses included in the accounting records of AquaMed have been attributed by management to the operations being retained by AquaMed, accordingly:

	Nine Months Ended September 30,
	2018			2017
Selling, general and administrative expenses
Compensation and benefits		$	301		$	151
Stock-based compensation			173			158
Professional fees			715			289
Other expenses and professional fees			544			177
Total selling, general and administrative expenses		$	1,733		$	775

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AQUAMED TECHNOLOGIES, INC.
(A SEGMENT OF ALLIQUA BIOMEDICAL, INC.)

NOTES TO CONDENSED UNAUDITED FINANCIAL STATEMENTS
FOR THE NINE MONTHS ENDED SEPTEMBER 30, 2018 AND 2017

Going Concern

As of September 30, 2018, the Company had a $0 cash balance. For the nine months ended September 30, 2018 and 2017, the Company incurred net losses of $1.3 million and $0.8 million, respectively. These factors raise substantial doubt as to the Company’s ability to continue as a going concern.

The Company expects to continue incurring losses for the foreseeable future and will need to raise additional capital to support ongoing operations.

Revenue Recognition

On January 1, 2018, the Company adopted Accounting Standards Codification (“ASC”) Topic 606, “Revenue from Contracts with Customers” (“ASC 606”). The core principle of ASC 606 requires that an entity recognize revenue to depict the transfer of promised goods or services to customers in an amount that reflects the consideration to which the Company expects to be entitled in exchange for those goods or services. ASC 606 defines a five-step process to achieve this core principle and, in doing so, it is possible more judgment and estimates may be required within the revenue recognition process than required under existing accounting principles generally accepted in the United States of America (“U.S. GAAP”) including identifying performance obligations in the contract, estimating the amount of variable consideration to include in the transaction price and allocating the transaction price to each separate performance obligation.

The Company adopted ASC 606 for all applicable contracts using the modified retrospective method, which would have required a cumulative-effect adjustment, if any, as of the date of adoption. The adoption of ASC 606 did not have a material impact on the Company’s condensed consolidated financial statements as of the date of adoption. As a result, a cumulative-effect adjustment was not required.

The Company recognizes revenue predominately from one type of revenue, contract manufacturing and recognizes an immaterial amount from the sale of products. Revenue from both contract manufacturing and products is recognized at the point where the customer obtains control of the goods and the Company satisfies its performance obligation, which generally is at the time it ships the product to the customer. To achieve this core principle, the Company applies the following five steps:

Step 1 — Identify the Contract with the Customer — A contract exists when (a) the parties to the contract have approved the contract and are committed to perform their respective obligations, (b) the entity can identify each party’s rights regarding the goods or services to be transferred, (c) the entity can identify the payment terms for the goods or services to be transferred, (d) the contract has commercial substance and it is probable that the entity will collect substantially all of the consideration to which it will be entitled in exchange for the goods or services that will be transferred to the customer.

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AQUAMED TECHNOLOGIES, INC.
(A SEGMENT OF ALLIQUA BIOMEDICAL, INC.)

NOTES TO CONDENSED UNAUDITED FINANCIAL STATEMENTS
FOR THE NINE MONTHS ENDED SEPTEMBER 30, 2018 AND 2017

Revenue Recognition – (continued)

Step 2 — Identify Performance Obligations in the Contract — Upon execution of a contract, the Company identifies as performance obligations each promise to transfer to the customer either (a) goods or services that are distinct or (b) a series of distinct goods or services that are substantially the same and have the same pattern of transfer to the customer. To the extent a contract includes multiple promised goods or services, the Company must apply judgement to determine whether the goods or services are capable of being distinct within the context of the contract. If these criteria are not met, the goods or services are accounted for as a combined performance obligation.

Step 3 — Determine the Transaction Price — The transaction price is determined based on the consideration to which the Company will be entitled in exchange for transferring products or services to the customer. Generally, all contracts include fixed consideration. If a contract did include variable consideration, the Company would determine the amount of variable consideration that should be included in the transaction price based on expected value method. Variable consideration would be included in the transaction price, if in the Company’s judgement, it is probable that a significant future reversal of cumulative revenue under the contract would not occur.

Step 4 — Allocate the Transaction Price — After the transaction price has been determined, the next step is to allocate the transaction price to each performance obligation in the contract. If the contract only has one performance obligation, the entire transaction price will be applied to that obligation. If the contract has multiple performance obligations, the transaction price is allocated to the performance obligations based on the relative standalone selling price (SSP) at contract inception.

Step 5 — Satisfaction of the Performance Obligations (and Recognize Revenue) — When an asset is transferred, and the customer obtains control of the asset (or the services are rendered), the Company recognizes revenue. At contract inception, the Company determines if each performance obligation is satisfied at a point in time or over time. Revenue from both product sales and contract manufacturing is recognized at the point where the customer obtains control of the goods and the Company satisfies its performance obligation, which generally is at the time it ships the product to the customer.

Disaggregation of Revenue

The Company recognizes revenue predominately from contract manufacturing and recognizes an immaterial amount from products. Revenue from both products and contract manufacturing is recognized at the point where the customer obtains control of the goods and the Company satisfies its performance obligation, which generally is at the time it ships the product to the customer.

As of September 30, 2018, or December 31, 2017, the Company did not have any contract assets or contract liabilities from contracts with customers. During the nine months ended September 30, 2018 and 2017, there was no revenue recognized from performance obligations satisfied (or partially satisfied) in previous periods. As of September 30, 2018, there were no remaining performance obligations that the Company had not satisfied.

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AQUAMED TECHNOLOGIES, INC.
(A SEGMENT OF ALLIQUA BIOMEDICAL, INC.)

NOTES TO CONDENSED UNAUDITED FINANCIAL STATEMENTS
FOR THE NINE MONTHS ENDED SEPTEMBER 30, 2018 AND 2017

Inventory

Inventory consists of the following (in thousands):

	September 30, 2018			December 31, 2017
Raw materials		$	130		$	98
Work in process			53			—
Finished goods			—			—
Less: Inventory reserve for excess and slow moving inventory			—			(5)
Total		$	183		$	93

Accrued Expenses and Other Current Liabilities

Accrued expenses and other current liabilities consist of the following (in thousands):

	September 30, 2018			December 31, 2017
Salaries, benefits and incentive compensation		$	108		$	92
Professional fees			123			28
Other			25			27
Total accrued expenses and other current liabilities		$	256		$	147

Operating Leases

The Company leases one commercial manufacturing facility through an operating lease agreement for this facility located in Langhorne, Pennsylvania, through 2026. Tenant improvements are also included in leasehold improvements on the balance sheet.

Future minimum lease payments, excluding expense reimbursements, under noncancelable operating leases at September 30, 2018 are as follows (in thousands):

2018		52
2019		207
2020		207
2021		207
2022		207
Thereafter		639
Total	$	1,519

Concentration of Risk

Revenue for the nine months ended September 30, 2018 and 2017, and accounts receivable as of September 30, 2018 from the Company’s largest customer, was as follows:

	% of Total Revenue				Accounts Receivable September 30, 2018
Customer	2018		2017		Accounts Receivable September 30, 2018
A		63%		61%		54%
B		13%		20%		0%

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AQUAMED TECHNOLOGIES, INC.
(A SEGMENT OF ALLIQUA BIOMEDICAL, INC.)

NOTES TO CONDENSED UNAUDITED FINANCIAL STATEMENTS
FOR THE NINE MONTHS ENDED SEPTEMBER 30, 2018 AND 2017

Improvements and Equipment, net

Improvements and equipment consist of the following (in thousands):

	Useful Life (Years)	September 30, 2018			December 31, 2017
Machinery and equipment	3 – 10		$	2,893		$	2,893
Office furniture and equipment	3 – 10			49			56
Leasehold improvements	(A)			228			228
				3,170			3,177
Less: Accumulated depreciation and amortization				(2,891)			(2,655)
Improvements and equipment, net			$	279		$	522

(A)

Leasehold improvements are amortized over the shorter of the remaining lease term or estimated useful life.

Depreciation and Amortization expense was $243,000 and $230,000 for the nine months ended September 30, 2018 and 2017, respectively.

10.

Income Taxes

During the quarter ended September 30, 2018, the Company finalized its U.S. federal 2017 income tax return, which resulted in an immaterial change in the net deferred tax asset, before valuation allowance, as of the enactment date. The Company has not adjusted the provisional estimates recorded during period ended December 31, 2017 under SAB 118 and will complete the accounting for the income tax effects of the Act prior to the end of the one-year measurement period.

11.

Subsequent Event

On November 27, 2018, AquaMed Technologies, Inc. (“AquaMed”), a wholly-owned subsidiary of Alliqua BioMedical, Inc. (“Alliqua” or the “Company”), AQ TOP, LLC, a Delaware limited liability company and a wholly-owned subsidiary of AquaMed (“Merger Sub”), and TO Pharmaceuticals, LLC, a Delaware limited liability company (“TOP”), entered into an Agreement and Plan of Merger (the “Merger Agreement”), pursuant to which, among other things, subject to the satisfaction or waiver of the conditions set forth in the Merger Agreement, Merger Sub will merge with and into TOP, with TOP becoming a wholly-owned subsidiary of the AquaMed and the surviving company of the merger (the “Merger”) See Note 1 — Recent Developments.

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REPORT OF INDEPENDENT REGISTERED PUBLIC ACCOUNTING FIRM

To the Members and Board of Managers of
TO Pharmaceuticals LLC and Subsidiaries

Opinion on the Financial Statements

We have audited the accompanying consolidated balance sheets of TO Pharmaceuticals LLC and Subsidiaries (the “Company”) as of December 31, 2017 and 2016, the related consolidated statements of operations, member’s deficit and cash flows for each of the two years in the period ended December 31, 2017, and the related notes (collectively referred to as the “financial statements”). In our opinion, the financial statements present fairly, in all material respects, the financial position of the Company as of December 31, 2017 and 2016, and the results of its operations and its cash flows for each of the two years in the period ended December 31, 2017 in conformity with accounting principles generally accepted in the United States of America.

Explanatory Paragraph — Going Concern

The accompanying consolidated financial statements have been prepared assuming that the Company will continue as a going concern. As more fully described in Note 2, the Company has experienced recurring net losses and negative cash flows from operations since its inception. These conditions raise substantial doubt about the Company’s ability to continue as a going concern. Management’s plans in regard to these matters are also described in Note 2. The consolidated financial statements do not include any adjustments that might result from the outcome of this uncertainty.

Basis for Opinion

We conducted our audits in accordance with the standards of the PCAOB and in accordance with auditing standards generally accepted in the United States of America. Those standards require that we plan and perform the audits to obtain reasonable assurance about whether the financial statements are free of material misstatement, whether due to error or fraud. The Company is not required to have, nor were we engaged to perform, an audit of its internal control over financial reporting. As part of our audits we are required to obtain an understanding of internal control over financial reporting but not for the purpose of expressing an opinion on the effectiveness of the Company’s internal control over financial reporting. Accordingly, we express no such opinion.

/s/ Marcum llp
Marcum llp

We have served as the Company’s auditor since 2018.

New York, NY
January 8, 2019

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TO PHARMACEUTICALS LLC AND SUBSIDIARIES

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
For the Years Ended December 31, 2017 and 2016

Nature of Organization

TO Pharmaceuticals LLC (the “Company”), is a limited liability company formed in the state of Delaware. The Company was formed on October 21, 2015 with an unlimited duration or until dissolved. The Company’s equity is represented by Class A membership interest units (“Class A Units”) and Class B profit sharing interests. The Company is an early stage biopharmaceutical company engaged in the business of discovering, developing and commercializing drugs containing cannabinoids, which are based on a proprietary cannabinoid product platform, for the treatment of various diseases, disorders and medical conditions. The Company operates primarily through two subsidiaries, TO Pharmaceuticals USA LLC, a Delaware limited liability company (“TOPUSA”) in the United States, and Tikun Olam IP Ltd., a Cayman Islands corporation (“TOIP”), outside the United States. The Company’s subsidiaries own exclusive licenses to exploit the intellectual property rights of certain cannabinoids throughout the world (except the State of New York) for pharmaceutical products in their respective territories. See Note 3 — Related Party Transactions. All intercompany activity and balances between the Company and its subsidiaries have been eliminated in consolidation.

Summary of Significant Accounting Policies

Basis of Presentation

Through July 13, 2018, the Company was a wholly-owned subsidiary of T.O. Global LLC (“TOG”). These financials statements have been derived from the accounting records of TOG and present the Company and its consolidated subsidiaries on a standalone basis. On July 13, 2018, all of the outstanding membership interests in the Company were distributed by TOG, the Company’s former sole beneficial owner, to its members on a pro rata basis.

Management believes the assumptions underlying the Company’s stand-alone financial statements are reasonable. Nevertheless, the financial statements may not include all of the actual expenses that would have been incurred had the Company operated as a standalone company during the periods presented, and may not reflect the Company’s results of operations, financial position and cash flows had the Company operated as a standalone company during the periods presented. Actual costs that would have been incurred if the Company had operated as a standalone company would depend on multiple factors, including organizational structure and strategic decisions made in various areas.

TOG used a centralized approach to cash management and financing its operations, including the operations of the Company. Accordingly, none of the cash and cash equivalents of TOG have been allocated to the Company in the financial statements. Transactions between TOG and the Company are accounted for through Due to Affiliate.

Use of estimates

The preparation of financial statements in conformity with generally accepted accounting principles of the United States of America requires management to makes estimates that affect the amounts reported in the financial statements and accompanying notes. These estimates include the fair values of long-lived assets. Actual results could differ from those estimates.

Intangible Assets

Intangible assets consist of licenses and related costs. Costs related to licenses are capitalized and amortized over their estimated useful lives using the straight-line method.

Impairment of Long-lived assets

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TO PHARMACEUTICALS LLC AND SUBSIDIARIES

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
For the Years Ended December 31, 2017 and 2016

Summary of Significant Accounting Policies – (continued)

eventual disposition are less than it’s carrying amount. If an impairment exists, the resulting write-down would be the difference between the fair market value of the long-lived asset and the related net book value. No material impairments related to long-lived assets or amortized intangible assets were recorded during the years ended December 31, 2017 and 2016.

Income taxes

The financial statements do not include a provision for income taxes because the Company does not incur federal or state income taxes. Instead, its earnings and loses are included in the member’s income tax returns.

U.S. GAAP requires entities to evaluate measure, recognize and disclose any uncertain income tax positions taken on their income tax returns. Management has evaluated the impact of this standard on it financial statements and believes that there are no uncertain tax positions and the effects of adopting this standard are not material to the Company’s financial position or results of operations. As of December 31, 2017, no interest or penalties were required to be recorded. Management’s conclusions regarding uncertain tax positions may be subject to review and adjustment at a later date upon ongoing analysis of tax laws, regulations, and interpretations thereof, as well as other factors.

Research and Development expenses

In accordance with authoritative guidance, the Company charges research and development costs to operations as incurred. Research and development expenses consist of the costs of clinical trials and the Company’s medical advisory board, and does not include other personnel or other costs.

Going concern

The Company’s consolidated financial statements are prepared using accounting principles generally accepted in the United States of America applicable to a going concern that contemplates the realization of assets and liquidation of liabilities in the normal course of business.

The Company is an early stage company with no operating revenue to date. As of December 31, 2017, the Company was dependent on TOG for support and had no cash of its own. The Company has experienced recurring net losses and negative cash flows from operations since its inception. The Company incurred a net loss of approximately $738,000 and used approximately $625,000 of cash in its operations for the year ended December 31, 2017, and had a member’s deficit of approximately $1,798,000 as of December 31, 2017. The Company received the proceeds of $500,000 principal amount of convertible notes in November 2018 and has a remaining cash balance of approximately $360,000 as of December 21, 2018. (See Note 7 — Subsequent Events).

In the near term, the Company expects its net losses and cash used in operating activities to increase as compared to prior periods as it increases its development activities. The Company expects to incur additional losses as it continues to research and develop drug candidates and conduct pre-clinical and clinical trials, and in any event, until its revenues exceed its expenses. Even if the Company succeeds in obtaining regulatory approval to market its products, of which there are no assurances, it may still incur losses for the foreseeable future.

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TO PHARMACEUTICALS LLC AND SUBSIDIARIES

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
For the Years Ended December 31, 2017 and 2016

Summary of Significant Accounting Policies – (continued)

property or marketing rights, which could result in the receipt of only a portion of any revenue that may be generated from a partnered product or business. If adequate funds are not obtained, the Company may be required to reduce, curtail, or discontinue operations. There is no assurance that the Company’s cash flow will be adequate to satisfy its existing operating expenses and capital requirements. In addition, if the Company issues equity or convertible debt securities to raise additional funds, its existing members may experience substantial dilution, and the new equity or debt securities may have rights, preferences and privileges senior to those of the Company’s existing members.

These factors raise substantial doubt as to the Company’s ability to continue as a going concern for a period of at least one year from the date these financial statements are issued. The ability of the Company to continue as a going concern is dependent upon the Company’s successful efforts to raise additional capital or other financing. These financial statements do not include any adjustments for this uncertainty.

Recent Accounting Principles

In August 2018, the FASB issued ASU 2018-13, “Fair Value Measurement (Topic 820): Disclosure Framework — Changes to the Disclosure Requirements for Fair Value Measurement”. The amendments in this update improve the effectiveness of disclosures in the notes to the financial statements by facilitating clear communication of the information required by GAAP that is most important to users of each entity’s financial statements. The amendments in this Update apply to all entities that are required, under existing GAAP, to make disclosures about recurring or nonrecurring fair value measurements. The amendments in this update are effective for all entities for fiscal years beginning after December 15, 2019, and interim periods within those fiscal years. The Company does not expect that this guidance will have a material impact on its financial statements.

In July 2018, the FASB issued ASU 2018-11, “Leases (Topic 842): Target Improvements”. The amendments in this Update clarify which Topic (Topic 842 or Topic 606) applies for the combined component. Specifically, if the non-lease component or components associated with the lease component are the predominant component of the combined component, an entity should account for the combined component in accordance with Topic 606. Otherwise, the entity should account for the combined component as an operating lease in accordance with Topic 842. An entity that elects the lessor practical expedient also should provide certain disclosures. The standard is effective for annual reporting periods beginning after December 15, 2018, which for the Company will commence with the year beginning January 1, 2019, with early application permitted. The Company is currently evaluating the adoption of this guidance and does not expect that this guidance will have a material impact on its financial statements. The Company has not adopted this Standard and will do so when specified by the FASB.

In July 2018, the FASB issued ASU 2018-10, “Codification Improvements to Topic 842, Leases”. The amendments in this Update affect narrow aspects of the guidance issued in the amendments in Update 2016-02. The amendments in this Update related to transition do not include amendments from proposed Accounting Standards Update, Leases (Topic 842): Targeted Improvements, specific to a new and optional transition method to adopt the new lease requirements in Update 2016-02. That additional transition method will be issued as part of a forthcoming and separate Update that will result in additional amendments to transition paragraphs included in this Update to conform to the additional transition method. The standard is effective for annual reporting periods beginning after December 15, 2018, which for the Company will commence with the year beginning January 1, 2019, with early application permitted. The Company is currently evaluating the adoption of this guidance and does not expect that this guidance will have a material impact on its financial statements. The Company has not adopted this Standard and will do so when specified by the FASB.

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TO PHARMACEUTICALS LLC AND SUBSIDIARIES

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
For the Years Ended December 31, 2017 and 2016

Summary of Significant Accounting Policies – (continued)

On December 22, 2017 the U.S. government enacted significant changes to federal tax law following the passage of the Tax Cuts and Jobs Act (“the Act”). Following the enactment of the Act, the SEC staff issued Staff Accounting Bulletin No. 118, Income Tax Accounting Implications of the Tax Cuts and Jobs Act (“SAB 118”). The Company follows the guidance in SAB 118, which provides additional clarification regarding the application of US GAAP in situations where the Company does not have the necessary information available, prepared, or analyzed in reasonable detail to complete the accounting for certain income tax effects of the Act for the reporting period in which the Act was enacted. SAB 118 provides for a measurement period beginning in the reporting period that includes the Act’s enactment date and ending when the Company has obtained, prepared, and analyzed the information needed in order to complete the accounting requirements but in no circumstances, should the measurement period extend beyond one year from the enactment date. The Company has evaluated the Act and, based on the information available, does not anticipate it to have a material impact on its financial statements. However, further analysis of the estimates and guidance on the application of the law could result in revisions during the allowable one-year measurement period, as outlined in SAB 118.

In November 2015, the FASB issued Accounting Standards Update 2015-17, “Income Taxes (Topic 740): Balance Sheet Classification of Deferred Taxes” (“ASU 2015-07”), an update to accounting guidance to simplify the presentation of deferred income taxes. The guidance requires an entity to classify all deferred tax liabilities and assets, along with any valuation allowance, as noncurrent in the balance sheet. The guidance is effective for public companies with annual reporting periods beginning after December 15, 2016, including interim periods within that reporting period. Early application is permitted. The Company has elected to early adopt ASU 2015-17 during the year ended December 31, 2016 with retrospective application. The adoption of ASU 2015-17 did not have a material impact on the Company’s financial statements.

Related Party Transactions

The Company leases its offices on a month to month basis from TOG, our parent. The terms of the lease call for monthly base payments of $1,000. Total rent expense for the years ended December 31, 2017 and 2016 amounted to $12,000, for each of the years.

Due to affiliate totaled $2,154,310 and $1,528,917 at December 31, 2017 and 2016, respectively to TOG, our parent. These unsecured loans are due on demand with no interest. See Note 7 — Subsequent Events.

Pursuant to a 2015 agreement (“MOU”) between a principal equityholder of the Company’s parent (until July 13, 2018) and Tikun Olam Ltd., an Israeli corporation (“TOL”), an unrelated third party which pursuant to such agreement became a principal equityholder of the parent, (i) TOPUSA and TOL entered into a license agreement dated as of April 13, 2017, as amended (the “US Pharma License”) relating to the Company’s U.S. pharmaceutical business (the “U.S. Pharmaceutical Business”); and (ii) TOIP and TOL entered into a license agreement dated as of April 13, 2017, as amended (the “WW Pharma License”, and together with the US Pharma License, the “Pharma Licenses”) relating to the Company’s non-U.S. pharmaceutical business (the “Worldwide Pharmaceutical Business”; and together with the

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TO PHARMACEUTICALS LLC AND SUBSIDIARIES

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
For the Years Ended December 31, 2017 and 2016

Related Party Transactions – (continued)

U.S. Pharmaceutical Business, the “Pharmaceutical Business”). Pursuant to the Pharma Licenses, TOL granted an exclusive worldwide (other than the State of New York), perpetual, non-revocable, and sublicensable license to use TOL’s intellectual property, whenever developed, in connection with the Company’s Pharmaceutical Business. TOPUSA is permitted to use such intellectual property solely in the United States (except the State of New York) and TOIP is permitted to use such intellectual property anywhere in the world excluding the United States. Pursuant to the MOU, TOG and the Company paid or caused to be paid to TOL an aggregate of $500,000 on behalf of TOPUSA and TOIP. No royalties or other payments are required under the Pharma Licenses except a two percent (2%) royalty payable to TOL with respect to TOIP’s sale of over-the-counter pharmaceutical products outside the U.S. which reasonably compete with a non-pharmaceutical medical cannabis product with substantially similar composition of active components sold by TOL or any licensee of TOL (other than TOIP) conducting business in the applicable jurisdiction pursuant to an effective legal license, permit or similar authority. The Company capitalized the costs associated with the Pharma Licenses, including certain costs of acquisition.

In connection with the Company’s ownership interest in and sublicense to Tikkun Pharma, Inc. a Delaware corporation (“Tikkun Pharma”), in 2017 the Company incurred $17,000 of expenses for the account of Tikkun Pharma, for which it is entitled to be reimbursed. The amount outstanding as of December 31, 2017 was $17,000.

Intangible Assets

The Company purchased the perpetual Pharma Licenses in 2015 for $505,000 including cost of the acquisition. These licenses were placed into service beginning in 2016. The Company amortizes its licenses over their useful lives of 20 years, the estimated life of similar type of licenses in the industry. The Company recognized $25,250 of amortization expense related to the licenses for each of the years ended December 31, 2017 and 2016. At December 31, 2017 and 2016, accumulated amortization was $50,500 and $25,250, respectively. See Note 3 — Related Party Transactions.

The weighted average amortization period is 18 years and future amortization expense on intangible assets is anticipated to be as follows:

For the years ending December 31,
2018	$	25,250
2019		25,250
2020		25,250
2021		25,250
2022		25,250
Thereafter		328,250
	$	454,500

Commitments

The Company entered into an employment agreement dated March 9, 2016 with Sidney Taubenfeld to serve as an executive vice president of the Company for an annual salary of $168,000. The Company has also issued warrants to Mr. Taubenfeld to purchase 39,505 Class A Units, of which 15,135 are vested as of December 31, 2017, at an exercise price of $12.40 per Class A Unit.

The Company has issued a warrant to Bernard Sucher, a manager of TOP, which is exercisable for an aggregate of 11,187 Class A Units, half of which are exercisable at exercise prices of $15.11 and $45.32 per Class A Unit.

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TO PHARMACEUTICALS LLC AND SUBSIDIARIES

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
For the Years Ended December 31, 2017 and 2016

Commitments – (continued)

In 2017, the Company entered into three agreements to conduct clinical trials in Israel, pursuant to which it is obligated to pay an aggregate of $435,000, of which $120,00 was paid as of December 31, 2017 and $315,000 remained owing as of December 31, 2017.

Carve-out assumptions and allocations

The expenses of the Company for the year ended December 31, 2016, including executive compensation, have been allocated by management between the Company and TOG, based either on specific attribution of those expenses or, where necessary and appropriate, based on management’s best estimate of an appropriate proportional allocation. Commencing 2017, all expenses were reflected directly on the books and records of the Company.

The following expenses included in the accounting records of the Company have been attributed by management to the operations being retained by the Company and accordingly have been excluded from the results of operations of TOG:

	For the Period Ended December 31, 2016
Operating Expenses
Clinical Trials (R&D)			106,179
Medical Advisory Board (R&D)			—
Legal & Professional Fees			702,603
Other Operating Expenses			226,363
Total Expenses		$	1,035,145

Subsequent Events

As of January 2018, TOPUSA entered into an exclusive sublicense agreement (the “TP USA Sublicense Agreement”) with Tikkun Pharma, and TOIP entered into an exclusive sublicense agreement (the “TP WW Sublicense Agreement”; and together with the TP USA Sublicense Agreement, the “TP Sublicense Agreements”) with Tikkun Pharma, pursuant to which TOPUSA and TOIP each have granted a perpetual, non-revocable (subject to the terms of the TP Sublicense Agreements), fully paid, royalty-free, exclusive sublicense of TOL’s intellectual property and licenses of their own respective intellectual property, in their respective territories, in connection with the production, research, development, promotion, marketing, sale, distribution and commercialization of pharmaceutical products derived from such intellectual property relating to the prevention, management and treatment of autoimmune diseases, disorders or symptoms related thereto, other than (1) Crohn’s Disease, coeliac diseases, any type of colitis (including without limitation microscopic and ulcerative colitis), any and all digestive and irritable bowel disorders, together with any diseases, disorders or symptoms related thereto, and (2) all diseases and disorders, and symptoms thereof, using glatiramer acetate (also known as Copaxone), whether alone or in a combination with any product, including not limited to, CBD. The Company received a 50% ownership interest in Tikkun Pharma. Tikkun Pharma has failed to fulfill certain of its obligations to the Company, with respect to which the Company has not exercised any remedial action.

As of January 2018, TOPUSA entered into an exclusive sublicense agreement (the “JP USA Sublicense Agreement”) with Jay Pharma, Inc., a Canadian corporation (“Jay Pharma”), and TOIP entered into an exclusive sublicense agreement with Jay Pharma (the “JP WW Sublicense Agreement”; and together with the JP USA Sublicense Agreement, the “JP Sublicense Agreements”), pursuant to which TOPUSA and TOIP each have granted a perpetual, non-revocable (subject to the terms of the JP Sublicense Agreements), fully paid, royalty-free, exclusive sublicense of TOL’s intellectual property and licenses of their own

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TO PHARMACEUTICALS LLC AND SUBSIDIARIES

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
For the Years Ended December 31, 2017 and 2016

Subsequent Events – (continued)

respective intellectual property, in their respective territories, in connection with the production, research, development, promotion, marketing, sale, distribution and commercialization of pharmaceutical products derived from such intellectual property relating to the prevention, management and treatment of cancer and diseases, disorders or symptoms related thereto. TOP received a 50% ownership interest in Jay Pharma.

Subsequent to December 31, 2017, the Company entered into two agreements to conduct clinical trials in Israel, pursuant to which it is obligated to pay an aggregate of approximately $198,000.

In November 2018, the Company issued $500,000 principal amount of convertible promissory notes to four accredited investors. These Notes bear interest at a rate of 5% per annum, payable upon maturity at March 31, 2019, and convert automatically upon consummation of the Merger at a conversion price equal to 80% of the per share price in the Private Placement.

In September 2018, the Company agreed to permit the affiliate to convert its then aggregate $1,036,256 of these obligations into up to six percent (6%) of the fully diluted equity of the Company. In December 2018, this affiliate converted the Company’s aggregate $1,036,256 obligations to it into 39,721 Class A Units of the Company, which represented six percent (6%) of the fully diluted equity of the Company.

Proposed Merger

On November 27, 2018, the Company entered into an Agreement and Plan of Merger (the “Merger Agreement”) with AquaMed Technologies, Inc., a wholly-owned subsidiary of Alliqua BioMedical, Inc. (“Alliqua” or the “Parent”) and AQ TOP, LLC, a Delaware limited liability company and a wholly-owned subsidiary of AquaMed (“Merger Sub”), pursuant to which, among other things, subject to the satisfaction or waiver of the conditions set forth in the Merger Agreement, Merger Sub will merge with and into the Company, with the Company becoming a wholly-owned subsidiary of AquaMed and the surviving company of the merger (the “Merger”). The Merger is intended to qualify for federal income tax purposes as a tax-free contribution under the provisions of Section 351(a) of the Internal Revenue Code of 1986, as amended.

The Merger will occur after the consummation by Alliqua of the following steps:

(1)

(2)

(3)

(4)

Alliqua will consummate its previously announced reverse merger transaction with Adynxx, Inc. (“Adynxx”), pursuant to that certain Agreement and Plan of Merger and Reorganization, dated as of October 11, 2018, by and among Alliqua, Embark Merger Sub, Inc. and Adynxx.

At the effective time of the Merger, all of the outstanding membership units of the Company will be converted into the right to receive, in the aggregate, merger consideration consisting of shares of AquaMed common stock. Immediately after the effective time of the Merger and consummation of the Private Placement (as defined below), before giving effect to any fees payable in equity to financial advisors or other

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TO PHARMACEUTICALS LLC AND SUBSIDIARIES

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
For the Years Ended December 31, 2017 and 2016

Subsequent Events – (continued)

intermediaries, the current members of TOP and the third-party investors that participate in the Private Placement are expected to hold approximately 90% of the total number of shares of AquaMed common stock outstanding (on a fully diluted basis). The Merger will be accounted for as a reverse business combination with the Company being the accounting acquirer.

The consummation of the Merger is subject to certain customary and other conditions, including (i) the completion of the Separation and the Distribution, (ii) the effectiveness of the registration statement on Form S-1 to be filed with the SEC with respect to, and the approval for listing on the NASDAQ Capital Market of, the shares of AquaMed common stock to be issued in the Distribution and the Merger, (iii) receipt of binding commitments from third-party investors to consummate a private placement of AquaMed’s common stock in a minimum aggregate amount of $10 million immediately prior to the effective time of the Merger (the “Private Placement”) (iv) the accuracy of the parties’ representations and warranties and the performance of their respective covenants contained in the Merger Agreement, and (v) receipt of an independent third-party valuation of the AquaMed common stock to be issued in the Distribution.

Management

The Company has entered into an offer letter agreement dated October 19, 2018 with Seth Yakatan to serve as its chief executive officer for an annual salary of $150,000. Mr. Yakatan is also eligible to receive options for three percent (3%) of AquaMed’s outstanding stock after giving effect to the Merger and the Private Placement.

The Company has entered into a consulting agreement dated as of November 1, 2018 with Broom Street Associates to provide the services of Dr. Mitchell Glass as the Company’s chief medical officer, at an annual rate of $120,000, payable half in cash and half in equity.

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TO Pharmaceuticals LLC and Subsidiaries

Notes to the Condensed Consolidated Financial Statements
For the nine months ended September 30, 2018 and 2017

Nature of Organization

Summary of Significant Accounting Policies

Basis of Presentation

The accompanying condensed consolidated financial statements of the Company have been prepared in accordance with generally accepted accounting principles (“GAAP”) for interim financial information, which are the accounting principles that are generally accepted in the United States of America. Accordingly, they do not include all of the information and footnotes required by GAAP for complete financial statements. In the opinion of management, all adjustments (consisting of normal recurring accruals) considered necessary for a fair presentation have been included. These interim unaudited condensed financial statements should be read in conjunction with the Company’s audited financial statements and notes for the years ended December 31, 2017 and 2016 included elsewhere herein.

Use of Estimates

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TO Pharmaceuticals LLC and Subsidiaries

Notes to the Condensed Consolidated Financial Statements
For the nine months ended September 30, 2018 and 2017

Summary of Significant Accounting Policies – (continued)

Intangible Assets

Intangible assets consist of the licenses and related costs. Costs related to the licenses are capitalized and amortized over their estimated useful lives using the straight-line method.

Impairment of Long-lived assets

Management reviews long-lived assets for potential impairment whenever significant events or changes in circumstances indicate that the carrying amount of an asset may not be recoverable. An impairment exists when the estimated undiscounted cash flows expected to result from the use of an asset and its eventual disposition are less than it’s carrying amount. If an impairment exists, the resulting write-down would be the difference between the fair market value of the long-lived asset and the related net book value. No material impairments related to long-lived assets or amortized intangible assets were recorded during the nine months ended September 30, 2018 and 2017.

Research and Development Expenses

Income taxes

U.S. GAAP requires entities to evaluate measure, recognize and disclose any uncertain income tax positions taken on their income tax returns. Management has evaluated the impact of this standard on it financial statements and believes that there are no uncertain tax positions and the effects of adopting this standard are not material to the Company’s financial position or results of operations. As of September 30, 2018 and December 31, 2017, no interest or penalties were required to be recorded. Management’s conclusions regarding uncertain tax positions may be subject to review and adjustment at a later date upon ongoing analysis of tax laws, regulations, and interpretations thereof, as well as other factors.

Going concern

The Company’s condensed consolidated financial statements are prepared using accounting principles generally accepted in the United States of America applicable to a going concern that contemplates the realization of assets and liquidation of liabilities in the normal course of business.

The Company is an early stage company with no operating revenue to date. Through July 13, 2018, the Company was dependent on TOG for its support had no cash of its own. The Company has experienced recurring net losses and negative cash flows since its inception. The Company incurred a net loss of approximately $637,000 for the nine months ended September 30, 2018, and had a members’ deficit of approximately $2,435,000 as of September 30, 2018. The Company received the proceeds of $500,000 principal amount of convertible notes in November 2018 and has a remaining cash balance of approximately $360,000 as of December 21, 2018. (See Note 6 — Subsequent Events)

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TO Pharmaceuticals LLC and Subsidiaries

Notes to the Condensed Consolidated Financial Statements
For the nine months ended September 30, 2018 and 2017

Summary of Significant Accounting Policies – (continued)

clinical trials, and in any event, until its revenues exceed its expenses. Even if the Company succeeds in obtaining regulatory approval to market its products, of which there are no assurances, it may still incur losses for the foreseeable future.

Based on the Company’s current financial situation, it may have difficulty continuing its operations at its current level, or at all, if it does not raise additional financing in the near future. The Company intends to raise funds through private placements, public offerings or other financings. Sources of debt financing may result in high interest expense or be difficult to procure and would increase the liabilities and future cash commitments of the Company. Any financing, if available, may be on unfavorable terms, and the Company may be forced to relinquish rights to its proprietary compounds, technology or other intellectual property or marketing rights, which could result in the receipt of only a portion of any revenue that may be generated from a partnered product or business. If adequate funds are not obtained, the Company may be required to reduce, curtail, or discontinue operations. There is no assurance that the Company’s cash flow will be adequate to satisfy its existing operating expenses and capital requirements. In addition, if the Company issues equity or convertible debt securities to raise additional funds, its existing members may experience substantial dilution, and the new equity or debt securities may have rights, preferences and privileges senior to those of the Company’s existing members.

Related Party Transactions

The Company leases its offices on a month-to-month basis from TOG. The terms of the lease call for monthly base payments of $1,000. Total rent expense amounted to $9,000 for each of the nine-month periods ended September 30, 2018 and 2017.

Due to affiliate totaled $2,558,936 and $2,154,310 at September 30, 2018 and December 31, 2017, respectively to TOG, the Company’s former parent. These unsecured loans are due on demand with no interest. In September 2018, the Company agreed to permit this affiliate to convert its then aggregate $1,036,256 of these obligations into up to six percent (6%) of the fully diluted equity of the Company.

In connection with the Company’s ownership interest in and sublicense to Tikkun Pharma, Inc. a Delaware corporation (“Tikkun Pharma”), through September 30, 2018, the Company incurred $76,500 of expenses for the account of Tikkun Pharma, for which it is entitled to be reimbursed. The amount outstanding as of September 30, 2018 and December 31, 2017 was $93,500 and $17,000, respectively.

Intangible Assets

The Company purchased the perpetual Pharma Licenses (as defined below) in 2015 for $505,000 including cost of the acquisition. These licenses were placed into service beginning in 2016. The Company amortizes its licenses over their useful lives of 20 years, the estimated life of similar type of licenses in the industry. The Company recognized $18,938 of amortization expense related to the licenses for each of the nine-month periods ended September 30, 2018 and 2017. See Note 3 — Related Party Transactions.

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TO Pharmaceuticals LLC and Subsidiaries

Notes to the Condensed Consolidated Financial Statements
For the nine months ended September 30, 2018 and 2017

Intangible Assets – (continued)

The weighted average amortization period is 18 years and future amortization expense on intangible assets is anticipated to be as follows:

For the years ending December 31,
2018	$	6,312
2019		25,250
2020		25,250
2021		25,250
2022		25,250
Thereafter		328,251
	$	435,563

Commitments

The Company has issued a warrant to Bernard Sucher, a manager of the Company, which is exercisable for 11,187 Class A Units, half of which are exercisable at exercise prices of $15.11 and $45.32 per Class A Unit.

Through September 30, 2018, the Company entered into five agreements to conduct clinical trials in Israel, pursuant to which it is obligated to pay an aggregate of approximately $633,000, of which approximately $137,000 was paid as of September 30, 2018 and approximately $496,000 remained owing as of September 30, 2018.

As of January 2018, TOPUSA entered into an exclusive sublicense agreement (the “TP USA Sublicense Agreement”) with Tikkun Pharma, and TOIP entered into an exclusive sublicense agreement (the “TP WW Sublicense Agreement”; and together with the TP USA Sublicense Agreement, the “TP Sublicense Agreements”) with Tikkun Pharma, pursuant to which TOPUSA and TOIP each have granted a perpetual, non-revocable (subject to the terms of the TP Sublicense Agreements), fully paid, royalty-free, exclusive sublicense of the intellectual property licensed (the “Pharma Licenses”) by the Company from Tikun Olam Ltd., an Israeli corporation (“TOL”) and licenses of their own respective intellectual property, in their respective territories, in connection with the production, research, development, promotion, marketing, sale, distribution and commercialization of pharmaceutical products derived from such intellectual property relating to the prevention, management and treatment of autoimmune diseases, disorders or symptoms related thereto, other than (1) Crohn’s Disease, coeliac diseases, any type of colitis (including without limitation microscopic and ulcerative colitis), any and all digestive and irritable bowel disorders, together with any diseases, disorders or symptoms related thereto, and (2) all diseases and disorders, and symptoms thereof, using glatiramer acetate (also known as Copaxone), whether alone or in a combination with any product, including not limited to, CBD. The Company received a 50% ownership interest in Tikkun Pharma. Tikkun Pharma has failed to fulfill certain of its obligations to the Company, with respect to which the Company has not exercised any remedial action.

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TO Pharmaceuticals LLC and Subsidiaries

Notes to the Condensed Consolidated Financial Statements
For the nine months ended September 30, 2018 and 2017

Commitments – (continued)

TOIP each have granted a perpetual, non-revocable (subject to the terms of the JP Sublicense Agreements), fully paid, royalty-free, exclusive sublicense of TOL’s intellectual property and licenses of their own respective intellectual property, in their respective territories, in connection with the production, research, development, promotion, marketing, sale, distribution and commercialization of pharmaceutical products derived from such intellectual property relating to the prevention, management and treatment of cancer and diseases, disorders or symptoms related thereto. TOP received a 50% ownership interest in Jay Pharma.

Subsequent Events

In December 2018, an affiliate of the Company converted the Company’s aggregate $1,036,256 obligations to it into 39,721 Class A Units of the Company, which represented six percent (6%) of the fully diluted equity of the Company.

Proposed Merger

The Merger will occur after the consummation by Alliqua of the following steps:

(1)

(2)

(3)

(4)

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TO Pharmaceuticals LLC and Subsidiaries

Notes to the Condensed Consolidated Financial Statements
For the nine months ended September 30, 2018 and 2017

Subsequent Events – (continued)

The consummation of the Merger is subject to certain customary and other conditions, including (i) the completion of the Separation and the Distribution, (ii) the effectiveness of the registration statement on Form S-10 to be filed with the SEC with respect to, and the approval for listing on the NASDAQ Capital Market of, the shares of AquaMed common stock to be issued in the Distribution and the Merger, (iii) receipt of binding commitments from third-party investors to consummate a private placement of AquaMed’s common stock in a minimum aggregate amount of $10 million immediately prior to the effective time of the Merger (the “Private Placement”) (iv) the accuracy of the parties’ representations and warranties and the performance of their respective covenants contained in the Merger Agreement, and (v) receipt of an independent third-party valuation of the AquaMed common stock to be issued in the Distribution.

Management

The Company has entered into an offer letter agreement dated October 19, 2018 with Seth Yakatan to serve as its chief executive officer for an annual salary of $150,000. Mr. Yakatan is also eligible to receive options for three percent(3%) of AquaMed’s outstanding stock after giving effect to the Merger and the Private Placement.

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PART II

INFORMATION NOT REQUIRED IN PROSPECTUS

Item 13. Other Expenses of Issuance and Distribution

The following table sets forth the costs and expenses, other than the underwriting discounts, payable by the registrant in connection with the registration of its common stock. All amounts are estimates except the Securities and Exchange Commission registration fee.

Item	Amount to Be Paid
Securities and Exchange Commission registration fee		$	65.33
Blue Sky fees and expenses			*
Legal fees and expenses			*
Accounting fees and expenses			*
Printing expenses			*
Miscellaneous			*
Total		$	*

To be filed by amendment

Item 14. Indemnification of Directors and Officers

Section 145 of the Delaware General Corporation Law provides that a corporation may indemnify directors and officers as well as other employees and individuals against expenses (including attorneys’ fees), judgments, fines and amounts paid in settlement in connection with any threatened, pending or completed actions, suit or proceeding, whether civil, criminal, administrative or investigative, in which such person is made a party by reason of the fact that the person is or was a director, officer, employee or agent of the corporation (other than an action by or in the right of the corporation — a “derivative action”), if such person acted in good faith and in a manner such person reasonably believed to be in or not opposed to the best interests of the corporation and, with respect to any criminal action or proceeding, had no reasonable cause to believe such person’s conduct was unlawful. A similar standard is applicable in the case of derivative actions, except that indemnification extends only to expenses (including attorneys’ fees) incurred in connection with the defense or settlement of such action, and the statute requires court approval before there can be any indemnification where the person seeking indemnification has been found liable to the corporation. The statute provides that it is not exclusive of other indemnification that may be granted by a corporation’s bylaws, disinterested director vote, stockholder vote, agreement or otherwise.

•

for any breach of a director’s duty of loyalty to us and our stockholders;

•

for any act or omission not in good faith or that involves intentional misconduct or a knowing violation of law;

•

under Section 174 of the Delaware General Corporation Law (unlawful payment of dividends or redemption of shares); or

•

for any breach of a director’s duty of loyalty to us or our stockholders.

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Item 15. Recent Sales of Unregistered Securities

None.

Item 16. Exhibits and Financial Statement Schedules

(a)

Exhibits

See the Exhibit Index immediately preceding the signature page to this registration statement, which is incorporated by reference herein.

(b)

Financial Statement Schedules:

No financial statement schedules are provided because the information called for is not required or is shown either in the financial statements or the notes thereto.

Item 17. Undertakings.

The undersigned registrant hereby undertakes:

(1)

To file, during any period in which offers or sales are being made, a post-effective amendment to this registration statement: (i) To include any prospectus required by Section 10(a)(3) of the Securities Act of 1933; (ii) To reflect in the prospectus any facts or events arising after the effective date of the registration statement (or the most recent post-effective amendment thereof) which, individually or in the aggregate, represent a fundamental change in the information set forth in the registration statement. Notwithstanding the foregoing, any increase or decrease in volume of securities offered (if the total dollar value of securities offered would not exceed that which was registered) and any deviation from the low or high end of the estimated maximum offering range may be reflected in the form of prospectus filed with the Commission pursuant to Rule 424(b) if, in the aggregate, the changes in volume and price represent no more than a 20% change in the maximum aggregate offering price set forth in the “Calculation of Registration Fee” table in the effective registration statement; and (iii) To include any material information with respect to the plan of distribution not previously disclosed in the registration statement or any material change to such information in the registration statement.

(2)

That, for the purpose of determining any liability under the Securities Act of 1933, each such post-effective amendment shall be deemed to be a new registration statement relating to the securities offered herein, and the offering of such securities at that time shall be deemed to be the initial bona fide offering thereof.

(3)

To remove from registration by means of a post-effective amendment any of the securities being registered which remain unsold at the termination of the offering.

(4)

That, for the purpose of determining liability under the Securities Act to any purchaser, if such registrant is subject to Rule 430C, each prospectus filed pursuant to Rule 424(b) as part of a registration statement relating to an offering, other than registration statements relying on

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Rule 430B or other than prospectuses filed in reliance on Rule 430A, shall be deemed to be part of and included in the registration statement as of the date it is first used after effectiveness. Provided, however, that no statement made in a registration statement or prospectus that is part of the registration statement or made in a document incorporated or deemed incorporated by reference into the registration statement or prospectus that is part of the registration statement will, as to a purchaser with a time of contract of sale prior to such first use, supersede or modify any statement that was made in the registration statement or prospectus that was part of the registration statement or made in any such document immediately prior to such date of first use

(5)

That, for the purpose of determining liability of the registrant under the Securities Act of 1933 to any purchaser in the initial distribution of the securities, the undersigned registrant undertakes that in a primary offering of securities of such undersigned registrant pursuant to this registration statement, regardless of the underwriting method used to sell the securities to the purchaser, if the securities are offered or sold to such purchaser by means of any of the following communications, the undersigned registrant will be a seller to the purchaser and will be considered to offer or sell such securities to such purchaser: (i) Any preliminary prospectus or prospectus of the undersigned registrant relating to the offering required to be filed pursuant to Rule 424; (ii) Any free writing prospectus relating to the offering prepared by or on behalf of the undersigned registrant or used or referred to by the undersigned registrant; (iii) The portion of any other free writing prospectus relating to the offering containing material information about the undersigned registrant or its securities provided by or on behalf of the undersigned registrant; and (iv) Any other communication that is an offer in the offering made by the undersigned registrant to the purchaser.

Insofar as indemnification for liabilities arising under the Securities Act of 1933 may be permitted to directors, officers and controlling persons of the registrant pursuant to the foregoing provisions, or otherwise, the registrant has been advised that in the opinion of the Securities and Exchange Commission such indemnification is against public policy as expressed in the Act and is, therefore, unenforceable. In the event that a claim for indemnification against such liabilities (other than the payment by the registrant of expenses incurred or paid by a director, officer or controlling person of the registrant in the successful defense of any action, suit or proceeding) is asserted by such director, officer or controlling person in connection with the securities being registered, the registrant will, unless in the opinion of its counsel the matter has been settled by controlling precedent, submit to a court of appropriate jurisdiction the question whether such indemnification by it is against public policy as expressed in the Act and will be governed by the final adjudication of such issue.

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SIGNATURES

Pursuant to the requirements of the Securities Act of 1933, the registrant has duly caused this Registration Statement on Form S-1 to be signed on its behalf by the undersigned, hereunto duly authorized, in the City of Langhorne, State of Pennsylvania, on January 9, 2019.

AQUAMED TECHNOLOGIES, INC.

By:

/s/ DAVID I. JOHNSON

Name: David I. Johnson
Title: Chief Executive Officer

POWER OF ATTORNEY

KNOW ALL MEN BY THESE PRESENTS, that each person whose signature appears below hereby constitutes and appoints each of David I. Johnson and Joseph Warusz his or her true and lawful attorney-in-fact and agent, with full power of substitution and resubstitution, for him or her and in his or her name, place and stead, in any and all capacities, to sign any and all amendments (including post-effective amendments) to this registration statement, and to file the same, with exhibits thereto, and other documents in connection therewith, with the Securities and Exchange Commission, granting unto said attorney-in-fact and agent full power and authority to do and perform each and every act and thing requisite and necessary to be done, as fully to all intents and purposes as he might or could do in person, hereby ratifying and confirming all that said attorney-in-fact and agent or either of them, or their or his or her substitute or substitutes, may lawfully do or cause to be done by virtue hereof.

Pursuant to the requirements of the Securities Act of 1933, as amended, this registration statement has been signed by the following persons in the capacities and on the dates indicated.

Signature	Title	Date
/s/ DAVID I. JOHNSON David I. Johnson	Director and Chief Executive Officer (Principal Executive Officer)	January 9, 2019
/s/ JOSEPH WARUSZ Joseph Warusz	Chief Financial Officer (Principal Financial and Accounting Officer)	January 9, 2019

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	AUDITED FINANCIAL STATEMENTS OF AQUAMED:
	Report of Independent Registered Public Accounting Firm					F-2
	Balance Sheets					F-3
	Statements of Operations					F-4
	Statements of Changes in Parent’s Net Investment					F-5
	Statements of Cash Flows					F-6
	Notes to the Financial Statements					F-7
	UNAUDITED CONDENSED INTERIM FINANCIAL STATEMENTS OF AQUAMED:
	Condensed Balance Sheets					F-18
	Condensed Statements of Operations					F-19
	Condensed Statement of Changes in Parent’s Net Investment					F-20
	Condensed Statements of Cash Flows					F-21
	Notes to the Condensed Financial Statements					F-22
	AUDITED CONSOLIDATED FINANCIAL STATEMENTS OF TOP:
	Report of Independent Registered Public Accounting Firm					F-30
	Consolidated Balance Sheets					F-31
	Consolidated Statements of Operations					F-32
	Consolidated Statements of Member’s Deficit					F-33
	Consolidated Statements of Cash Flows					F-34
	Notes to the Consolidated Financial Statements					F-35
	UNAUDITED CONDENSED CONSOLIDATED INTERIM FINANCIAL STATEMENTS OF TOP:
	Condensed Consolidated Balance Sheets					F-43
	Condensed Consolidated Statements of Operations					F-44
	Condensed Consolidated Statement of Members’ Deficit					F-45
	Condensed Consolidated Statements of Cash Flows					F-46
	Notes to the Condensed Consolidated Financial Statements					F-47

(in thousands)	Historical TOP for the Year Ended December 31, 2017			Historical AquaMed for the Year Ended December 31, 2017			Transaction Adjustments			Pro Forma Combined
Revenue		$	—		$	1,992		$	—		$	1,992
Loss before income taxes			(738)			(969)			—			(1,707)
Income tax benefit			—			16			—			16
Net loss		$	(738)		$	(953)		$	—		$	(1,691)

	For the Nine Months Ended September 30, 2018
Parent’s net investment, beginning of period		$	625
Net Loss			(1,323)
Advances from Parent			1,237
Parent’s net investment, end of period		$	539

	2017			2016
ASSETS
Current Assets
Other receivable-related party		$	17,000		$	—
Total Current Assets			17,000			—
Intangible Assets
Licenses, net of accumulated amortization			454,500			479,750
Total Assets		$	471,500		$	479,750
LIABLILITIES
Current Liabilities
Accounts payable		$	65,155		$	11,128
Accrued expenses			50,000			—
Due to affiliate			2,154,310			1,528,917
Total Current Liabilities			2,269,465			1,540,045
MEMBER’S DEFICIT
Member’s Deficit			(1,797,965)			(1,060,295)
Total Liabilities and Member’s Deficit		$	471,500		$	479,750

	2017			2016
Balance, Beginning of Year		$	(1,060,295)		$	100
Net Loss			(737,670)			(1,060,395)
Balance, End of Year		$	(1,797,965)		$	(1,060,295)

	2017			2016
Cash Flow from Operating Activities:
Net loss		$	(737,670)		$	(1,060,395)
Adjustments to reconcile net loss to net cash used in operating activities:
Amortization			25,250			25,250
Changes in operating assets and liabilities:
Other receivable-related party			(17,000)			—
Accounts payable			54,027			11,128
Accrued expenses			50,000			—
Net cash used by operating activities			(625,393)			(1,024,017)
Cash Flows from Financing Activities
Due to affiliate			625,393			1,024,017
Net cash provided by financing activities			625,393			1,024,017
Net Increase (Decrease) in Cash			—			—
Cash, Beginning of the Year			—			—
Cash, End of the Year		$	—		$	—

	September 30, 2018 (Unaudited)			December 31, 2017
ASSETS
Current Assets
Other receivable-related party		$	93,500		$	17,000
Total Current Assets			93,500			17,000
Intangible Assets
Licenses, net of accumulated amortization			435,563			454,500
Total Assets		$	529,063		$	471,500
LIABLILITIES
Current Liabilities
Accounts payable		$	89,471		$	65,155
Accrued expenses			315,509			50,000
Due to affiliate			2,558,936			2,154,310
Total Current Liabilities			2,963,916			2,269,465
MEMBERS’ DEFICIT
Members’ Deficit			(2,434,853)			(1,797,965)
Total Liabilities and Members’ Deficit		$	529,063		$	471,500

	2018 (Unaudited)			2017 (Unaudited)
Operating Expenses
Selling, general and administrative		$	296,779		$	450,936
Research and development			340,109			73,822
Total Operating Expenses			636,888			524,758
Net Loss from Operations		$	(636,888)		$	(524,758)
Net Loss		$	(636,888)		$	(524,758)

	2018 (Unaudited)
Balance as of January 31, 2018		$	(1,797,965)
Net Loss			(636,888)
Balance at September 30, 2018		$	(2,434,853)

	Exhibit Number			Exhibit Description
	2.1			Agreement and Plan of Merger, dated November 27, 2018, by and among AquaMed Technologies, Inc., TO Pharmaceuticals, LLC and AQ TOP, LLC (incorporated by reference to Exhibit 2.1 to Alliqua BioMedical Inc.’s Form 8-K, filed with the SEC on November 28, 2018)*
	2.2			Amendment No. 1, dated January 8, 2019 to Agreement and Plan of Merger
	2.3			Form of Asset Contribution and Separation Agreement between Alliqua BioMedical, Inc. and AquaMed Technologies, Inc.*
	2.4			Form of Tax Matters Agreement between Alliqua BioMedical, Inc. and AquaMed Technologies, Inc.*
	2.5			Form of Bill of Sale and Assignment and Assumption Agreement between Alliqua BioMedical, Inc. and AquaMed Technologies, Inc.†*
	3.1			Certificate of Incorporation of AquaMed Technologies, Inc. (as currently in effect)
	3.2			Certificate of Amendment to Certificate of Incorporation of AquaMed Technologies, Inc.
	3.3			Form of Amended and Restated Certificate of Incorporation of AquaMed Technologies, Inc.†
	3.4			Bylaws of AquaMed Technologies, Inc. (as currently in effect)
	3.5			Form of Amended and Restated Bylaws of AquaMed Technologies, Inc.†
	5.1			Opinion of Haynes and Boone, LLP†
	10.1			Assignment and Amended and Restated Lease, dated as of January 25, 2002, by and between 2150 Cabot LLC, Embryo Development Corporation and Hydrogel Design Systems, Inc.
	10.2			Amendment to Lease, dated as of February 23, 2007, by and between 2150 Cabot LLC and Hydrogel Design Systems, Inc.
	10.3			Third Amendment to Lease, dated as of February 27, 2009, by and between Exeter 2150 Cabot, L.P and Hydrogel Design Systems, Inc.
	10.4			Assignment and Assumption of Lease Agreement, dated as of February 27, 2009, by and among Exeter 2150 Cabot, L.P, Hydrogel Design Systems, Inc. and Aquamed Technologies, Inc.
	10.5			Fourth Amendment to Lease, dated as of July 24, 2013, by and between Exeter 2150 Cabot, L.P and Aquamed Technologies, Inc.
	10.6			License Agreement, dated as of April 13, 2017, by and between Tikun Olam Ltd. and TO Pharmaceuticals USA LLC*
	10.7			Amendment dated December 9, 2018, to License Agreement, dated as of April 13, 2017, by and between Tikun Olam Ltd. and TO Pharmaceuticals USA LLC
	10.8			License Agreement, dated as of April 13, 2017, by and between Tikun Olam Ltd. and Tikun Olam IP Ltd.*
	10.9			Amendment dated December 9, 2018, to License Agreement, dated as of April 13, 2017, by and between Tikun Olam Ltd. and Tikun Olam IP Ltd
	10.10			Amended and Restated Sublicense Agreement, dated as of January 12, 2018, by and between TO Pharmaceuticals USA LLC and Tikkun Pharma, Inc.
	10.11			Amended and Restated Sublicense Agreement, dated as of January 12, 2018, by and between Tikun Olam IP Ltd. and Tikkun Pharma, Inc.
	10.12			Sublicense Agreement, dated as of January 12, 2018, by and between TO Pharmaceuticals USA LLC and Jay Pharma, Inc.

	Exhibit Number			Exhibit Description
	10.13			Sublicense Agreement, dated as of January 12, 2018, by and between Tikun Olam IP Ltd. and Jay Pharma, Inc.
	10.14			Master Intercompany Services Agreement, dated as of January 1, 2018, by and among T.O. Global LLC, TO Holding Group LLC, Tikun Olam LLC, TO Pharmaceuticals LLC and Israel Liaison Holding Group Ltd.*
	10.15			Letter Agreement, dated September 26, 2018, by and between T.O. Global LLC and TO Pharmaceuticals LLC*
	10.16			Employment Agreement, dated as of March 9, 2016, by and between TO Pharmaceuticals LLC and Sidney Taubenfeld*
	10.17			Management Consulting Agreement dated October 19, 2018 between TO Pharmaceutical LLC and Seth Yakatan*
	10.18			Consulting Agreement dated as of November 1, 2018 between TO Pharmaceuticals LLC and Broom Street Associates, LLC
	10.19			Warrant, dated March 9, 2016 issued to Sidney Taubenfeld.*
	10.20			Warrant, dated November 1, 2018, issued to Bernard Sucher, exercisable at $15.11 per Class A Unit*
	10.21			Warrant, dated November 1, 2018, issued to Bernard Sucher, exercisable at $45.32 per Class A Unit*
	21.1			List of Subsidiaries of AquaMed Technologies, Inc.
	23.1			Consent of Marcum, LLP with respect to the financial statements of AquaMed Technologies, Inc.
	23.2			Consent of Marcum, LLP with respect to the financial statements of TO Pharmaceuticals, LLC
	23.3			Consent of Haynes and Boone, LLP (contained in Exhibit 5.1)†
	24.1			Powers of Attorney (included on the signature page of this Registration Statement)