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HROW US Equity

Harrow, Inc.Health Care · Pharmaceutical Preparations · CIK 1360214 · FY ends Dec 31
$41.64
+2.12 (+5.36%)
USD · as of 2026-08-19 · marketstack

HROW · 10-K · period ended 2023-12-31

← all HROW documents
filed 2024-03-19 · EDGAR original ↗

Our rendering of the filing — original pagination and typography are not reproduced, and tables are reduced to their short label cells (the figures live on FA). Nothing is summarized: every line below is the filing's own text.

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UNITED

STATES

SECURITIES

AND EXCHANGE COMMISSION

Washington,

D.C. 20549

FORM

10-K

(Mark

One)

For the fiscal year ended December 31, 2023

OR

For

the transition period from to

Commission

File Number: 001-35814

HARROW,

INC.

(Exact

name of registrant as specified in its charter)

102

Woodmont Blvd., Suite 610

Nashville,

TN37205

(Address

of Principal Executive Offices)(Zip Code)

(615)733-4730

(Registrant’s

telephone number, including area code)

Securities

registered pursuant to Section 12(b) of the Act:

Title of Each Class Trading Symbol Name of Each Exchange on Which Registered

Common Stock, $0.001 par value per share HROW The Nasdaq Stock Market LLC

8.625% Senior Notes due 2026 HROWL The Nasdaq Stock Market LLC

11.875% Senior Notes due 2027 HROWM The Nasdaq Stock Market LLC

Securities

registered pursuant to Section 12(g) of the Act: None

Indicate

by check mark if the registrant is a well-known seasoned issuer, as defined in Rule 405 of the Securities Act. Yes ☐ No☒

Indicate

by check mark if the registrant is not required to file reports pursuant to Section 13 or Section 15(d) of the Exchange Act. Yes ☐

No ☒

Indicate

by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange

Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2)

has been subject to such filing requirements for the past 90 days. Yes ☒ No ☐

Indicate

by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule

405 of Regulation S-T (§ 229.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant

was required to submit such files). Yes ☒ No ☐

Indicate

by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a 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 13(a) of the Exchange Act. ☐

Indicate

by check mark whether the registrant has filed a report on and attestation to its management’s assessment of the effectiveness

of its internal control over financial reporting under Section 404(b) of the Sarbanes-Oxley Act (15 U.S.C. 7262(b)) by the registered

public accounting firm that prepared or issued its audit report. ☐

If

securities are registered pursuant to Section 12(b) of the Act, indicate by check mark whether the financial statements of the registrant

included in the filing reflect the correction of an error to previously issued financial statements. ☐

Indicate

by check mark whether any of those error corrections are restatements that required a recovery analysis of incentive-based compensation

received by any of the registrant’s executive officers during the relevant recovery period pursuant to § 240.10D-1(b).

Indicate

by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes ☐ No☒

As

of June 30, 2023, the last business day of the registrant’s most recently completed second fiscal quarter, the aggregate market

value of the common stock held by non-affiliates of the registrant was approximately $464 million, based on the closing price of $19.04

for the registrant’s common stock as quoted on The Nasdaq Stock Market LLC on that date. For purposes of this calculation, it has

been assumed that shares of common stock held by each director, each officer and each person who owns 10% or more of the outstanding

common stock of the registrant are held by affiliates of the registrant. The treatment of these persons as affiliates for purposes of

this calculation is not conclusive as to whether such persons are affiliates of the registrant for any other purpose.

As

of March 18, 2024, there were 35,362,642 shares of the registrant’s common stock outstanding.

Portions

of the registrant’s definitive Proxy Statement for its 2024 Annual Meeting of Stockholders to be held on June 13, 2024 are incorporated

by reference in Part III of this Annual Report on Form 10-K, to the extent stated herein.

TABLE

OF CONTENTS

Page

PART I

Item 1. Business 3

Item 1A. Risk Factors 19

Item 1B. Unresolved Staff Comments 51

Item 1C. Cybersecurity 51

Item 2. Properties 52

Item 3. Legal Proceedings 52

Item 4. Mine Safety Disclosures 52

PART II

Item 6. [Reserved] 52

Item 7A. Quantitative and Qualitative Disclosures About Market Risk 66

Item 8. Financial Statements and Supplementary Data 67

Item 9A. Controls and Procedures 67

Item 9B. Other Information 68

Item 9C. Disclosure Regarding Foreign Jurisdictions that Prevent Inspections 68

PART III

Item 10. Directors, Executive Officers and Corporate Governance 68

Item 11. Executive Compensation 68

Item 14. Principal Accountant Fees and Services 68

PART IV

Item 15. Exhibits, Financial Statement Schedules 69

SIGNATURES 74

As

used in this Annual Report on Form 10-K (this “Annual Report”), unless indicated or the context requires otherwise, the terms

the “Company,” “Harrow,” “we,” “us” and “our” refer to Harrow, Inc. and its

consolidated subsidiaries.

In

addition to historical information, the following discussion contains forward-looking statements regarding future events and our future

performance. In some cases, you can identify forward-looking statements by terminology such as “will,” “may,”

“should,” “expects,” “plans,” “anticipates,” “believes,” “estimates,”

“predicts,” “forecasts,” “potential” or “continue” or the negative of these terms or

other comparable terminology. All statements made in this Annual Report other than statements of historical fact are forward-looking

statements. These forward-looking statements involve risks and uncertainties and reflect only our current views, expectations and assumptions

with respect to future events and our future performance. If risks or uncertainties materialize or assumptions prove incorrect, actual

results or events could differ materially from those expressed or implied by such forward-looking statements. Risks that could cause

actual results to differ from those expressed or implied by the forward-looking statements we make include, among others, risks related

to: liquidity or results of operations; our ability to successfully implement our business plan, develop and commercialize our proprietary

formulations in a timely manner or at all, identify and acquire additional proprietary formulations, manage our pharmacy operations,

service our debt, obtain financing necessary to operate our business, recruit and retain qualified personnel, manage any growth we may

experience and successfully realize the benefits of our previous acquisitions and any other acquisitions and collaborative arrangements

we may pursue; competition from pharmaceutical companies, outsourcing facilities and pharmacies; general economic and business conditions,

including inflation and supply chain challenges; regulatory and legal risks and uncertainties related to our pharmacy operations and

the pharmacy and pharmaceutical business in general; physician interest in and market acceptance of our current and any future formulations

and compounding pharmacies generally; our limited operating history; and the other risks and uncertainties described under the heading

“Risk Factors” in Part I, Item 1A of this Annual Report. You should not place undue reliance on forward-looking statements.

Forward-looking statements speak only as of the date they are made and, except as required by law, we undertake no obligation to revise

or publicly update any forward-looking statement for any reason.

We

have registered trademarks, copyrights and/or pending trademark and copyright applications for a number of proprietary names in the United

States, including, but not limited to: VEVYE®, IHEEZO®, VIGAMOX®, ILEVRO®, TRIESENCE®, ImprimisRx®,

LessDrops®, Dropless Cataract Surgery®, Klarity-C®, MKO Melt®, and Simple

Drops®. We may choose to pursue trademark protection in other jurisdictions for one or more of these or other marks in

the future. All other trademarks, service marks and trade names included or incorporated by reference into this Annual Report, are the

property of their respective owners.

PART

I

ITEM

1. BUSINESS

Overview

We

are a leading eyecare pharmaceutical company engaged in the discovery, development, and commercialization of innovative ophthalmic pharmaceutical

products for the U.S. market. Harrow helps U.S. eyecare professionals preserve the gift of sight by making its comprehensive portfolio

of prescription and non-prescription pharmaceutical products accessible and affordable to millions of Americans each year. We own commercial

rights to one of the largest portfolios of branded ophthalmic pharmaceutical products in North America, all of which are marketed under

the Harrow name. We also own and operate ImprimisRx, one of the nation’s leading ophthalmology-focused pharmaceutical-compounding

businesses. In addition, we have a non-controlling equity interest in Melt Pharmaceuticals, Inc. (“Melt”), and two other

companies that began as subsidiaries of Harrow and were subsequently carved-out of our corporate structure and deconsolidated from our

financial statements.

Branded

Ophthalmic Pharmaceuticals

Over

the past few years, we have invested in broadening our product portfolio of FDA-approved products. Our investments in this regard have

led to the pursuit and completion of several announced transactions, all of which are focused on eyecare pharmaceuticals primarily for

the U.S. and Canadian markets. We believe that our continued investments in these and other products will result in our ability to provide

more physician prescribers and their patients with access to a complete portfolio of affordable eyecare pharmaceuticals to address their

clinical needs. We own U.S. commercial rights to the following products:

We

also own U.S. rights to some discontinued products. In February 2024, we announced that we out-licensed Canadian rights for VERKAZIA,

Cationorm® PLUS (a preservative-free formulation for dry eye or allergy relief), VEVYE, ZERVIATE and IHEEZO to Apotex Inc. (“Apotex”).

We also own worldwide rights to NATACYN and FRESHKOTE.

ImprimisRx

ImprimisRx

is our ophthalmology-focused pharmaceutical compounding businesses. From its inception in 2014, ImprimisRx, whose business consists of

integrated research and development, production, dispensing/distribution, sales, marketing, and customer-service capabilities, has offered

ophthalmologist and optometrist customers and their patients access to critical medicines to meet their clinical needs. Initially, ImprimisRx

focused exclusively on compounded medications to serve needs unmet by commercially available drugs. Our compounded medications include

various combinations of drugs formulated into one bottle and numerous preservative-free formulations. Depending on the formulation, the

regulations of a specific state, and ultimately the needs of the patient, ImprimisRx products may be dispensed as patient-specific medications

from our 503A pharmacy, or for in-office use, made according to current good manufacturing practices (“cGMPs”) or other guidance

documents from the U.S. Food and Drug Administration (the “FDA”), in our FDA-registered New Jersey outsourcing facility.

Our current ophthalmology formulary includes over 30 compounded formulations, many of which are patented or patent-pending, that are

customizable for the specific needs of a patient. We make our formulations available at prices that are, in most cases, lower than non-customized

commercial drugs. ImprimisRx’s customer base has grown to include more than 10,000 U.S. eyecare-dedicated prescribers and institutions.

Carved-Out

Subsidiaries (De-Consolidated Businesses)

We

have ownership interests in Melt, Surface Ophthalmics, Inc. (“Surface”) and Eton Pharmaceuticals, Inc. (“Eton”)

and hold royalty interests in some of Surface’s and Melt’s drug candidates. These companies are pursuing market approval

for their drug candidates under the Federal Food Drug and Cosmetic Act (the “FDCA”), including in some instances under the

abbreviated pathway described in Section 505(b)(2), which permits the submission of a new drug application (an “NDA”) where

at least some of the information required for approval comes from studies not conducted by or for the applicant and for which the applicant

has not obtained a right of reference.

Melt

Pharmaceuticals, Inc.

Melt

is a clinical-stage pharmaceutical company focused on the development and commercialization of proprietary non-intravenous, sedation

and anesthesia therapeutics for human medical procedures in hospital, outpatient, and in-office settings. Melt is seeking regulatory

approval for its proprietary technologies, where possible. In December 2018, we entered into an Asset Purchase Agreement with Melt (the

“Melt Asset Purchase Agreement”), pursuant to which Harrow assigned to Melt the underlying intellectual property for Melt’s

current pipeline, including its lead drug candidate MELT-300. The core intellectual property Melt owns is a patented series of combination

non-opioid sedation drug formulations that we estimate to have many clinical applications.

MELT-300

is a novel, sublingually delivered, non-IV, opioid-free drug candidate being developed for procedural sedation. In February 2021, Melt

announced data from, and the successful completion of, its Phase 1 study. In December 2022, Melt announced topline data from its Phase

2 study for MELT-300 as set forth below:

● MELT-300’s safety profile was generally comparable to the placebo arm.

Melt

expects to begin Phase 3 program activities in 2024, which will consist of a single pivotal study comparing MELT-300 to sublingual midazolam

and placebo in subjects undergoing cataract surgery. Beginning in July 2023 through March 1, 2024, Melt had raised over $23,000,000 in

gross proceeds from the sale and issuance of Melt’s Series B Preferred Stock. We own 3,500,000 shares of Melt common stock, 2,260,000

shares of Melt’s Series B-1 Preferred Stock and 74,256 shares of Melt’s Series B Preferred Stock, which in aggregate represented

approximately 47% and 46% of Melt’s equity and voting interests issued and outstanding as of December 31, 2023 and March 1, 2024,

respectively.

Melt

is required to make mid-single digit royalty payments to the Company on net sales of MELT-300 while any patent rights remain outstanding,

subject to other conditions. Melt can require the Company to cease compounding like products at the time of FDA approval of MELT-300.

If approved, we do not expect a cessation of compounding like products to have a material impact on our operations and financial performance.

Surface

Ophthalmics, Inc.

Surface

is a clinical-stage pharmaceutical company focused on development and commercialization of innovative therapeutics for ocular surface

diseases. Surface is developing four product candidates at various stages of development for certain ocular surface related indications.

We

own 3,500,000 shares of Surface common stock, which represented approximately 20% of Surface’s equity and voting interests as of

December 31, 2023. Harrow owns mid-single-digit royalty rights on net sales on Surface’s drug candidates SURF-100, SURF-200 and

SURF-201.

Eton

Pharmaceuticals, Inc.

Eton

is an innovative pharmaceutical company focused on developing, acquiring, and commercializing treatments for rare diseases. Eton currently

commercializes ALKINDI SPRINKLE® and Carglumic Acid tablets and has additional rare disease products under development, including

dehydrated alcohol injection and the ZENEO® hydrocortisone autoinjector. In May 2017, we gave up our controlling interest in Eton.

We own 1,982,000 shares of Eton common stock, which represented less than 10% of Eton’s equity and voting interests issued and

outstanding as of December 31, 2023.

Pharmaceutical

Compounding Businesses

Pharmaceutical

Compounding

Pharmaceutical

compounding is the science of combining different active pharmaceutical ingredients (APIs), all of which are approved by the FDA (either

as a finished form product or as a bulk drug ingredient), and excipients to create specialized pharmaceutical preparations. Physicians

and healthcare institutions use compounded drugs when commercially available drugs do not optimally treat a patient’s needs. In

many cases, compounded drugs, such as ours, have wide market utility and may be clinically appropriate for large patient populations.

Examples of compounded formulations include medications with alternative dosage strengths or unique dosage forms, such as topical creams

or gels, suspensions, or solutions with more tolerable drug delivery vehicles.

Sales

revenue from our compounded products are derived from us making, selling and dispensing our compounded prescription drug formulations

as cash payment transactions between us and our end-user customers. As such, the majority of our commercial transactions for compounded

products do not involve distributors, wholesalers, insurance companies, pharmacy benefit managers or other middle parties. In regard

to our compounded formulations, by not being reliant on insurance company formulary inclusion and pharmacy benefit manager payment clawbacks,

we are able to simplify the prescription transaction process. We believe the outcome of our compounding business model is a simple transaction,

involving a patient-in-need, a physician’s diagnosis, a fair price and great service for a quality pharmaceutical product.

ImprimisRx

Compounding Facilities

Pharmaceutical

compounding businesses are governed by Sections 503A and 503B of the FDCA. Section 503A of the FDCA provides that a pharmacy is only

permitted to compound a drug for an individually identified patient based on a prescription for the patient and is only permitted to

distribute the drug interstate if the pharmacy is licensed to do so in the states where it is compounded and where the medication is

received.

Section

503B of the FDCA provides that a pharmacy engaged in preparing sterile compounded drug formulations may voluntarily elect to register

as an “outsourcing facility.” Outsourcing facilities are permitted to compound large quantities of drugs without a prescription

and distribute them out of state with certain limitations, such as the formulation appearing on the FDA’s drug shortage list or

the bulk drug substances contained in the formulations appearing on the FDA’s “clinical need” list. Entities voluntarily

registering with FDA as outsourcing facilities are subject to additional requirements that do not apply to compounding pharmacies (operating

under Section 503A of the FDCA), including adhering to standards such cGMPs or other FDA guidance documents and being subject to regular

FDA inspection.

We

operate two compounding facilities located in Ledgewood, New Jersey. Our New Jersey operations are comprised of two separate entities

and facilities, one of which is registered with the FDA as an outsourcing facility (“NJOF”) under Section 503B of the FDCA.

The other New Jersey facility (“RxNJ”) is a licensed pharmacy operating under Section 503A of the FDCA. All of our compounded

products that we sell, produce and dispense are made in the United States.

We

believe that, with our current compounding pharmacy facilities and licenses and FDA registration of NJOF, we have the infrastructure

to scale our business appropriately under the current regulatory landscape and meet the potential growth in demand we are targeting.

We plan to invest in one or both of our facilities to further their capacity and efficiencies. Also, we may seek to access greater pharmacy

and production related redundancy and markets through acquisitions, partnerships or other strategic transactions.

Sales

and Marketing

The

focus of our sales and marketing is in the U.S. We do, however, believe that our proprietary drug formulations, drug candidates and drug

products could have commercial appeal in international markets, and have engaged distributors and entered into out-licensing arrangements

for certain of our products and proprietary formulations in certain non-U.S. markets, including Canada. Our sales and marketing activities

consist primarily of efforts to educate doctors, ambulatory surgery centers, healthcare systems, hospitals and other users throughout

the U.S. about our branded drug products and compounded formulations. We expect that we may experience growth in the sales of our products

in future periods, particularly in light of our recent product launches and commercial campaigns. However, we may not be successful in

doing so, whether due to the safety, quality or availability of our products and proprietary compounded formulations, the size of the

markets for such products, which could be smaller than we expect, the timing of market entry relative to competitive products, the availability

of alternative compounded formulations or FDA-approved drugs, the price of our products relative to alternative products or the success

of our sales and marketing efforts, which is dependent on our ability to further build and continue to grow a qualified and adequate

internal sales function.

We

expect to continue to acquire and/or develop additional FDA-approved ophthalmic products that allow us to leverage our existing commercial

infrastructure to promote, sell, and ultimately bring these products to market. As we execute this strategy, we will continue to expand

our sales and marketing team, expertise and expenses.

Ophthalmology

Market

For

any ocular procedure, a surgeon may require drugs for sedation, dilation, anesthesia, inflammation and infection prevention, and ocular

surface preservation. The cataract surgery market continues to experience significant growth. According to Market Scope, approximately

4.8 million lens procedures were performed in the U.S. in 2021, 97% of which were cataracts, with the number expected to grow to 5.5

million lens procedures in 2026. Nearly 96% of the refractive surgery procedures performed are LASIK (laser in situ keratomileusis) surgeries,

an outpatient surgical procedure used to treat nearsightedness, farsightedness, and astigmatism. According to an article published in

2021 in Clinical Ophthalmology, an estimated 800,000 eyes were treated with laser correction surgery (such as LASIK) each year

for the previous ten years.

Dry

eye occurs when the eye does not produce enough tears, or when the tears are not of the correct consistency and evaporate too quickly.

Inflammation of the surface of the eye may also occur. According to a 2023 Market Scope report, there are 39 million people in

the U.S. that suffer from both signs and symptoms of dry eye, with 49% of diagnosed dry eye patients having moderate to severe dry eye.

The same report stated the global dry eye product market is expected to grow from $5.8 billion in 2023 to $7.5 billion in 2028. Dry eye

is among the most common conditions seen by eyecare professionals.

Intravitreal

injections are one of the most common procedures performed by ophthalmologists in the United States. According to a 2023 article published

in Healio, approximately 8 million intravitreal injections were expected to be performed that year. These injections are utilized

to administer critical medications into the eye that treat diseases including but not limited to proliferative diabetic retinopathy,

diabetic macular edema, wet age-related macular degeneration, neovascular glaucoma, retinal vein occlusions, intraocular tumors, and

endophthalmitis. In addition, products and product candidates are being developed and used to treat symptoms associated with an eye disease

known as geographic atrophy. Most of the medicines in these products and product candidates are administered via intravitreal injection.

Therefore, we believe as these products and product candidates gain commercial adoption, the number of annual intravitreal injections

should increase further and at an increased rate as compared to recent years.

Vitrectomy

is a surgical procedure undertaken by a specialist where the vitreous humor gel that fills the eye cavity is removed to provide better

access to the retina. This allows for a variety of repairs, including the removal of scar tissue, laser repair of retinal detachments

and treatment of macular holes. According to an October 2022 article published on the Cleveland Clinic website, U.S. surgeons perform

about 225,000 vitrectomies each year. The number is likely to continue to grow as eye care providers find more uses for vitrectomy.

Chronic

non-infectious uveitis affecting the posterior segment of the eye is an inflammatory disease that afflicts people of all ages, producing

swelling and destroying eye tissues, which can lead to severe vision loss and blindness. Based on internal estimates and information

published on the MedScape website (which was updated as of March 2023) that cites various ranges of prevalence of uveitis, we estimate

this disease affects approximately 100,000 people each year in the U.S. The standard of care treatment for this disease typically involves

the use of short-acting corticosteroids to reduce uveitic flares (such as TRIESENCE) followed by additional treatments of sustained release,

lower dose steroids to minimize the risk of further flares.

Competition

The

pharmaceutical and pharmacy industries are highly competitive. We compete against branded drug companies, generic drug companies, outsourcing

facilities and compounding pharmacies. We are smaller than some of our competitors, and we may lack the financial and other resources

needed to develop, produce, distribute, market and commercialize any of our branded products and proprietary formulations or compete

for market share in these sectors. The drug products available through branded and generic drug companies with which our products and

formulations compete have been approved for marketing and sale by the FDA and are required to be manufactured in facilities compliant

with cGMP standards. Although we prepare some of our compounded formulations in accordance with cGMP standards and our other formulations

are produced according to the standards provided by United States Pharmacopoeia (USP) Chapter <795> (“USP 795”) and

USP Chapter <797> (“USP 797”) and applicable state and federal law, our compounded formulations are not required to

be, and have not been, approved for marketing and sale by the FDA. As a result, some physicians may be unwilling to prescribe, and some

patients may be unwilling to use, our compounded formulations. Additionally, under federal and state laws applicable to our current compounding

pharmacy operations operating under Section 503A of the FDCA, we are not permitted to prepare significant amounts of a specific formulation

in advance of a prescription, compound quantities for office use or utilize a wholesaler for distribution of our formulations; instead,

our compounded formulations must be prepared and dispensed in connection with a physician prescription for an individually identified

patient. Pharmaceutical companies, on the other hand, are able to sell their FDA-approved products to large pharmaceutical wholesalers,

who can in turn sell to and supply hospitals and retail pharmacies. Even though we have registered NJOF with the FDA, our compounding

business may not be scalable on the scope available to our competitors that produce FDA-approved drugs, which may limit our potential

for profitable operations. These facets of our operations may subject our business to limitations our competitors offering only FDA-approved

drugs may not face.

Biotechnology

and related pharmaceutical technologies are subject to rapid and significant change. Our future success will depend in large part on

our ability to maintain a competitive position with respect to these technologies. Products developed by our competitors, including FDA-approved

drugs and compounded formulations created by other pharmacies, could render our products and technologies obsolete or unable to compete.

Any products that we develop may become obsolete before we recover expenses incurred in developing the products, which may require that

we seek additional funds that may or may not be available to continue our operations. The competitive environment requires an ongoing,

extensive search for medical and technological innovations and the ability to develop and market these innovations effectively, and we

may not be competitive with respect to these factors. Other competitive factors include the safety and efficacy of a product, the size

of the market for a product, the timing of market entry relative to competitive products, the availability of alternative compounded

formulations or approved drugs, the price of a product relative to alternative products, the availability of third-party reimbursement,

the success of sales and marketing efforts, brand recognition and the availability of scientific and technical information about a product.

Although we believe we are positioned to compete favorably with respect to many of these factors, if our proprietary formulations are

unable to compete with the products of our competitors, we may never gain a significant market share or achieve profitability.

Factors

Affecting Our Performance

We

believe the primary factors affecting our performance are our ability to increase revenues of our ophthalmic products, grow and gain

operating efficiencies in our pharmacy operations, successfully adjust our operations to account for any future regulatory-related restrictions,

optimize pricing and obtain reimbursement options for our ophthalmic products, and continue to pursue development and commercialization

opportunities for certain of our ophthalmology and other assets that we have not yet made commercially available or have been recently

launched. We believe we have built a tangible and intangible infrastructure that will allow us to scale revenues efficiently in the near

and long-term. All of these activities will require increased costs and other resources, which we may not have or be able to obtain from

operations or other sources. See “Liquidity and Capital Resources” below.

Medicare,

Medicaid and Other Reimbursement Options

Sales

in the United States of our marketed products are dependent, in large part, on the availability and extent of reimbursement from third-party

payors, including private payor healthcare and insurance programs, health maintenance organizations, pharmacy benefit management companies,

and government programs such as Medicare and Medicaid, see also Part I, Item 1A. “Risk Factors” for additional risks related

to reimbursement and government programs.

We

participate in, and have certain price reporting obligations to, the Medicaid Drug Rebate program, state Medicaid supplemental rebate

program(s), and other governmental pricing programs. We also have obligations to report the average sales price for certain drugs to

the Medicare program. Under the Medicaid Drug Rebate program, we are required to pay a rebate to each state Medicaid program for our

covered outpatient drugs that are dispensed to Medicaid beneficiaries and paid for by a state Medicaid program as a condition of having

federal funds being made available for our drugs under Medicaid and Part B of the Medicare program.

Medicare

is a federal program that is administered by the federal government that covers individuals age 65 and over or that are disabled as well

as those with certain health conditions. Medicare Part B generally covers drugs that must be administered by physicians or other health

care practitioners; are provided in connection with certain durable medical equipment; or are certain oral anti-cancer drugs and certain

oral immunosuppressive drugs. Medicare Part B pays for such drugs under a payment methodology based on the average sales price of the

drugs. Manufacturers, including us, are required to report average sales price information to the Centers for Medicare & Medicaid

Services (“CMS”) on a quarterly basis. The manufacturer-submitted information may be used by CMS to calculate Medicare payment

rates. Starting in 2023, manufacturers are now required to pay refunds to Medicare for single-source drugs or biological products, or

biosimilar biological products, reimbursed under Medicare Part B and packaged in single-dose containers or single-use packages for units

of discarded drug reimbursed by Medicare Part B in excess of 10% of total allowed charges under Medicare Part B for that drug. Manufacturers

that fail to pay refunds could be subject to civil monetary penalties. Further, starting in 2023, the Inflation Reduction Act of 2022

(“IRA”) established a Medicare Part B inflation rebate scheme, effective in 2023, under which, generally speaking, manufacturers

will owe rebates if the average sales price of a Part B drug increases faster than the pace of inflation. Failure to timely pay a Part

B inflation rebate is subject to a civil monetary penalty.

The

IRA also created a drug price negotiation program under which, after being on the market for a certain period of time, the prices for

certain high Medicare spending drugs and biological products provided to Medicare patients without generic or biosimilar competition

will be capped by reference to, among other things, a specified non-federal average manufacturer price, starting in 2026. Failure to

comply with requirements under the drug price negotiation program is subject to an excise tax and a civil monetary penalty. This or any

other legislative change could impact the market conditions for our products.

IHEEZO

and TRIESENCE are covered under Medicare Part B and we may develop other drug candidates and/or acquire drug products that are also covered

under Medicare Part B. In February 2023, we announced that CMS had issued a permanent, product specific J-code for IHEEZO (J2403) which

will become effective under the Healthcare Procedure Coding System (HCPCS) on April 1, 2023. TRIESENCE has a permanent product specific

J-code (J3300) as well, which physicians can use for reimbursement purposes of that product. New drugs approved by the FDA that are used

in surgeries performed in a hospital outpatient departments or ambulatory surgical centers may receive a transitional pass-through reimbursement

under Medicare, provided they meet certain criteria, including a “not insignificant” cost criterion. Pass-through status

allows for separate payment (i.e., outside the packaged payment rate for the surgical procedure) under Medicare Part B, which consists

of Medicare reimbursement for a drug based on a defined formula for calculating the minimum fee that a manufacturer may charge for the

drug. Under current regulations of CMS, pass-through status applies for a period of three years; which is measured from the date Medicare

makes its first pass-through payment for the product. Following the three-year period, the product would be incorporated into the cataract

bundled payment system, which could significantly reduce the pricing for that product. Temporary pass-through reimbursement for IHEEZO

was awarded by CMS and made effective in the second quarter of 2023. Following the expiration of pass-through status, under current CMS

policy, non-opioid pain management surgical drugs when used on Medicare Part B patients in an outpatient setting can qualify for ongoing

separate payments. CMS’ current non-opioid separate payment policy, like other CMS policies, can be changed by CMS through its

annual rulemaking and comment process.

We

are also working to ensure our continued access to the Medicare market for the ambulatory surgery center (ASC), hospital and outpatient

department (HOPD), and in-office use markets for IHEEZO. In this regard, we are designing and intend to execute, during 2024, clinical

studies to build data sets that could be presented to CMS to extend our temporary pass-through period for IHEEZO in ASCs and HOPDs. We

also met with CMS in January 2024 to request clarification related to its anesthesia billing policy which has historically not allowed

for the separate billing of anesthesia services in the physician’s office. During the meeting we requested that CMS clarify that

J-Code 2403, IHEEZO’s permanent J-Code, is appropriate to be billed for the anesthesia product itself (i.e., IHEEZO in our case)

in the physician’s office setting. As of the date of this Annual Report, we have not received feedback from CMS following our meeting

in January 2024.

Medicaid

is a joint federal and state program that is administered by the states for low-income and disabled beneficiaries. Medicaid rebates are

based on pricing data reported by us on a monthly and quarterly basis to CMS, the federal agency that administers the Medicaid and Medicare

programs. These data include the average manufacturer price and, in the case of innovator products, the best price for each drug which,

in general, represents the lowest price available from the manufacturer to any entity in the U.S. in any pricing structure, calculated

to include all sales and associated rebates, discounts, and other price concessions. The amount of the rebate is adjusted upward if the

average manufacturer price increases at a faster rate than inflation (measured by reference to the Consumer Price Index – Urban).

The rebate was previously capped at 100% of the average manufacturer price, but effective January 1, 2024, this cap on the rebate was

removed, and our rebate liability could increase accordingly.

If

we become aware that our reporting for a prior quarter was incorrect or has changed as a result of recalculation of the pricing data,

we are obligated to resubmit the corrected data for up to three years after those data originally were due, which revisions could affect

our rebate liability for prior quarters. The federal Patient Protection and Affordable Care Act (the “PPACA” or “Health

Care Reform Law”) made significant changes to the Medicaid Drug Rebate program, and CMS issued a final regulation, which became

effective on April 1, 2016, to implement the changes to the Medicaid Drug Rebate program under the PPACA. Effective in 2022, CMS modified

Medicaid Drug Rebate program regulations to, among other things, permit reporting multiple best price figures with regard to value-based

purchasing arrangements and provide definitions for “line extension,” “new formulation,” and related terms with

the practical effect of expanding the scope of drugs considered to be line extensions.

Civil

monetary penalties can be applied if we are found to have knowingly submitted any false pricing or other information to the government,

if we are found to have made a misrepresentation in the reporting of our average sales price, or if we fail to submit the required data

on a timely basis. Such conduct also could be grounds for CMS to terminate our Medicaid drug rebate agreement, in which case federal

payments may not be available under Medicaid or Medicare Part B for our covered outpatient drugs.

Federal

law requires that any company that participates in the Medicaid Drug Rebate program also participate in the Public Health Service’s

340B drug pricing program (the “340B program”) in order for federal funds to be available for the manufacturer’s drugs

under Medicaid and Medicare Part B. The 340B program, which is administered by the Health Resources and Services Administration (“HRSA”),

requires participating manufacturers to agree to charge statutorily defined covered entities no more than the 340B “ceiling price”

for the manufacturer’s covered outpatient drugs. Covered entities include hospitals that serve a disproportionate share of financially

needy patients, community health clinics, and other entities that receive certain types of grants under the Public Health Service Act.

The PPACA expanded the list of covered entities to include certain free-standing cancer hospitals, critical access hospitals, rural referral

centers, and sole community hospitals, but exempts “orphan drugs” from the ceiling price requirements for these covered entities.

The 340B ceiling price is calculated using a statutory formula, which is based on the average manufacturer price and Medicaid rebate

amount for the covered outpatient drug as calculated under the Medicaid Drug Rebate program. In general, products subject to Medicaid

price reporting and rebate liability are also subject to the 340B ceiling price calculation and discount requirement.

HRSA

issued a final regulation regarding the calculation of the 340B ceiling price and the imposition of civil monetary penalties on manufacturers

that knowingly and intentionally overcharge covered entities, which became effective on January 1, 2019. It is currently unclear how

HRSA will apply its enforcement authority under this regulation. Any charge by HRSA that we have violated the requirements of the regulation

could result in civil monetary penalties. Moreover, under a final regulation effective January 13, 2021, HRSA established a new administrative

dispute resolution (“ADR”) process for claims by covered entities that a manufacturer has engaged in overcharging, and by

manufacturers that a covered entity violated the prohibitions against diversion or duplicate discounts. Such claims are to be resolved

through an ADR panel of government officials rendering a decision that could be appealed only in federal court. An ADR proceeding could

subject us to onerous procedural requirements and could result in additional liability. On November 30, 2022, HRSA issued a notice of

proposed rulemaking that proposes several changes to the ADR process. HRSA also implemented a price reporting system under which we are

required to report our 340B ceiling prices to HRSA on a quarterly basis, which then publishes those prices to 340B covered entities.

In addition, legislation could be passed that would further expand the 340B program to additional covered entities or would require participating

manufacturers to agree to provide 340B discounted pricing on drugs used in an inpatient setting.

In

order to be eligible to have our products paid for with federal funds under the Medicaid and Medicare Part B programs and purchased by

certain federal agencies and grantees, we participate in the U.S. Department of Veterans Affairs (“VA”) Federal Supply Schedule

(“FSS”) pricing program. FSS participation is required for our products to be purchased by the VA, Department of Defense

(“DoD”), Coast Guard, and Public Health Service (“PHS”). Prices for innovator drugs purchased by the VA, DoD,

Coast Guard, and PHS are subject to a cap (known as the “Federal Ceiling Price”) equal to 76% of the annual non-federal average

manufacturer price (“non-FAMP”) minus, if applicable, an additional discount. The additional discount applies if non-FAMP

increases more than inflation (measured by reference to the Consumer Price Index - Urban). We also participate in the Tricare Retail

Pharmacy Program, under which we pay quarterly rebates to DoD for prescriptions of our innovator drugs dispensed to Tricare beneficiaries

through Tricare Retail network pharmacies. The governing statute provides for civil monetary penalties for failure to provide information

timely or for knowingly submitting false information to the government.

Medicare

Part D provides coverage to enrolled Medicare patients for self-administered drugs (i.e., drugs that are not administered by a physician).

Medicare Part D is administered by private prescription drug plans approved by the U.S. government and, subject to detailed program rules

and government oversight, each drug plan establishes its own Medicare Part D formulary for prescription drug coverage and pricing, which

the drug plan may modify from time to time. The prescription drug plans negotiate pricing with manufacturers and pharmacies, and may

condition formulary placement on the availability of manufacturer discounts. In addition, manufacturers, including us, are required to

provide to CMS a 70% discount on brand name prescription drugs utilized by Medicare Part D beneficiaries when those beneficiaries are

in the coverage gap phase of the Part D benefit design. The IRA includes a sunset provision with respect to the coverage gap discount

program starting in 2025 and replaces it with a new manufacturer discount program. In addition, as of October 2022, the IRA established

a Medicare Part D inflation rebate scheme under which, manufacturers will generally owe additional rebates if the average manufacturer

price of a Part D drug increases faster than the pace of inflation. Failure to timely pay a Part D inflation rebate is subject to a civil

monetary penalty.

Private

payor healthcare and insurance providers, health maintenance organizations, and pharmacy benefit managers in the United States are adopting

more aggressive utilization management techniques and are increasingly requiring significant discounts and rebates from manufacturers

as a condition to including products on formulary with favorable coverage and copayment/coinsurance. These payors may not cover or adequately

reimburse for use of our products or may do so at levels that disadvantage them relative to competitive products.

Our

proprietary ophthalmic compounded formulations are primarily available on a cash-pay basis and generally are not subject to Medicare,

Medicaid, or other payor-related initiatives.

Intellectual

Property

Our

success and ability to compete depends upon our ability to protect our intellectual property. We conduct a fulsome analysis of the intellectual

property landscape prior to acquiring rights to formulations and filing patent applications. In addition, as of March 1, 2024, we owned

and/or licensed more than 50 total issued and pending patent applications, which include U.S.-issued patents, international-issued patents,

and U.S. and foreign/international patent pending applications. We expect to file additional patent applications in the U.S. and pursue

patent protection for certain of our formulations in other important international jurisdictions in the future.

As

of March 1, 2024, we had, on a worldwide basis, more than 100 issued trademarks, pending trademark and copyright applications, or registered

copyrights and/or trademarks. We also rely on unpatented trade secrets and know-how and continuing technological innovation in order

to develop our products and formulations, which we seek to protect, in part, by confidentiality agreements with our employees, consultants,

collaborators and others, including certain service providers. We also have invention or patent assignment agreements with our current

employees and certain consultants. However, our employees and consultants may breach these agreements, and we may not have adequate remedies

for any breach, or our trade secrets may otherwise become known or be independently discovered by competitors. In addition, inventions

relevant to us could be developed by a person not bound by an invention assignment agreement with us, in which case we may have no rights

to use the applicable invention.

The

following table lists our outstanding material patents in the U.S. for certain branded products, general subject matter and latest expiry

date. One or more patents with the same or earlier expiry dates may fall under the same general subject matter and are not listed separately.

Product General Subject Matter Expiration

IHEEZO Methods using topical formulations September 2038

Governmental

Regulation

Our

business is subject to federal, state and local laws, regulations, and administrative practices, including, among others: federal, state

and local licensure and registration requirements concerning the operation of pharmacies and the practice of pharmacy; the Health Insurance

Portability and Accountability Act of 1996 (“HIPAA”); the Health Care Reform Law; statutes and regulations of the FDA, the

U.S. Federal Trade Commission (the “FTC”), the U.S. Drug Enforcement Administration and the U.S. Consumer Product Safety

Commission, as well as regulations promulgated by comparable state agencies concerning the sale, advertisement and promotion of the products

we sell. The regulatory and quality compliance environment for compounded drugs has become significantly more rigorous, complex and strict

since the passage of The Drug Quality and Security Act of 2013 (the “DQSA”). The complexity of the current state and federal

regulatory environment, as well as the expected continued evolution of state and federal laws governing pharmaceutical compounding, have

presented, and will continue to present, potentially significant challenges to our business model and the fulfillment of our mission

as a company. Below are descriptions of some of the various federal and state laws and regulations which may govern or impact our current

and planned operations.

FDA

New Drug Application Process

As

discussed in other sections of this Annual Report, we are pursuing, and may continue to pursue, alone or with project partners, FDA approval

to market and sell one or more of our product candidates through the FDA’s NDA process. As a condition of approval, the FDA or

other regulatory authorities may require further studies, including Phase 4 post-marketing studies, to provide additional data. Other

post-marketing studies may be required to gain approval for the use of a product as a treatment for clinical indications other than those

for which the product was initially tested and approved. Also, the FDA or other regulatory authorities require post-marketing reporting

to monitor the adverse effects of a drug. Results of post-marketing programs may limit or expand the further marketing of a product.

The

FDA closely regulates the post-approval marketing and promotion of drugs, including standards and regulations for direct-to-consumer

advertising, off-label promotion, industry-sponsored scientific and educational activities and promotional activities involving the Internet.

A company can make only those claims relating to safety and efficacy that are approved by the FDA. Failure to comply with these requirements

can result in adverse publicity, warning letters, corrective advertising, fines and potential civil and criminal penalties.

Section

505(b)(2) New Drug Applications

As

an alternate path for FDA approval of new indications or new formulations of previously-approved products, a company may file a Section

505(b)(2) NDA instead of a “stand-alone” or “full” NDA. Section 505(b)(2) of the FDCA was enacted as part of

the Drug Price Competition and Patent Term Restoration Act of 1984, otherwise known as the Hatch-Waxman Amendments. Section 505(b)(2)

permits the submission of an NDA where at least some of the information required for approval comes from studies not conducted by or

for the applicant and for which the applicant has not obtained a right of reference. Some examples of products that may be allowed to

follow a Section 505(b)(2) path to approval are drugs that have a new dosage form, strength, route of administration, formulation or

indication.

The

Hatch-Waxman Amendments permit the applicant to rely upon certain published nonclinical or clinical studies conducted for an approved

product or the FDA’s conclusions from prior review of such studies. The FDA may require companies to perform additional studies

or measurements to support any changes from the approved product. The FDA may then approve the new product for all or some of the labeled

indications for which the reference product has been approved, as well as for any new indication supported by the Section 505(b)(2) application.

While references to nonclinical and clinical data not generated by the applicant or for which the applicant does not have a right of

reference are allowed, all development, process, stability, qualification and validation data related to the manufacturing and quality

of the new product must be included in an NDA submitted under Section 505(b)(2).

To

the extent that the Section 505(b)(2) applicant is relying on the FDA’s conclusions regarding studies conducted for an already

approved product, the applicant is required to certify to the FDA concerning any patents listed for the approved product in the FDA’s

Approved Drug Products with Therapeutic Equivalence Evaluations, or Orange Book. Specifically, the applicant must certify that: (i) the

required patent information has not been filed; (ii) the listed patent has expired; (iii) the listed patent has not expired, but will

expire on a particular date and approval is sought after patent expiration; or (iv) the listed patent is invalid or will not be infringed

by the new product. The Section 505(b)(2) application also will not be approved until any non-patent exclusivity, such as exclusivity

for obtaining approval of a new chemical entity, listed in the Orange Book for the referenced product has expired. Thus, the Section

505(b)(2) applicant may invest a significant amount of time and expense in the development of its products only to be subject to significant

delay and patent litigation before its products may be commercialized.

Pharmacy

Regulation

Our

pharmacy operations are regulated by both individual states and the federal government. Every state has laws and regulations addressing

pharmacy operations, including regulations relating specifically to compounding pharmacy operations. These regulations generally include

licensing requirements for pharmacists, pharmacy technicians and pharmacies, as well as regulations related to compounding processes,

safety protocols, purity, sterility, storage, controlled substances, recordkeeping and regular inspections, among other things. State

rules and regulations are updated periodically, generally under the jurisdiction of individual state boards of pharmacy. Failure to comply

with the state pharmacy regulations of a particular state could result in a pharmacy being prohibited from operating in that state, financial

penalties and/or becoming subject to additional oversight from that state’s board of pharmacy. In addition, many states are considering

imposing, or have already begun to impose, more stringent requirements on compounding pharmacies. If our pharmacy operations become subject

to additional licensure requirements, are unable to maintain their required licenses or if states place burdensome restrictions or limitations

Source: SEC EDGAR (public domain) · 10-K for the period ended 2023-12-31, filed 2024-03-19 · accession 0001493152-24-010518

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