10-K 0001104659-26-036286 (2026-03-30) vs 10-K 0001410578-25-000743 (2025-04-15)
| Section | Compared text | Words now | Changed |
| Risk Factors | Item 1A | 16,899 |
80.3% |
| MD&A | Item 7 | 4,301 |
77.8% |
| Legal Proceedings | Item 3, via Note 11 – Commitments and Contingencies | 1,041 |
81.4% |
| Accounting Policies | 10-K text (note not found) | 0 |
not compared |
The redline: what was cut and what was added
In each section, the paragraph that changed most, marked against last year's 10-K:
cut words struck through, new words highlighted and underlined.
Risk Factors 258 words changed in this paragraph; it is 35% similar to last year's version.
The secure processing, storage, maintenance, maintenance and transmission of this critical information is vital to our operations and business strategy, and we devote significant resources to protecting such information. Although we take measures to protect sensitive information from unauthorized access or disclosure, our information technology and infrastructure may be vulnerable to attacks by hackers or viruses, breaches, interruptions due to employee error, malfeasance, faulty password management, lapses in compliance with privacy and security mandates, or other disruptions. The risk of a security breach or disruption, particularly through cyber-attack or cyber intrusion, including by computer hackers, foreign governments and cyber terrorists, has generally increased as the number, intensity and sophistication of attempted attacks and intrusions from around the world have increased. Our IT networks and related systems are essential to the operation of our business and our ability to perform day-to-day operations. To the extent that any disruption or security breach were to result in a loss of or damage to our data or applications, or inappropriate disclosure of confidential or proprietary information, we could incur substantial liability. Although we make efforts to maintain the security and integrity of these types of IT networks and related systems, and we have implemented various measures to manage the risk of a security breach or disruption, there can be no assurance that our security efforts and measures will be effective or that attempted security breaches or disruptions would not be successful or damaging. Our information technology systems may have vulnerabilities, and we may not have the resources or technical sophistication to anticipate or prevent rapidly evolving types of cyberattacks, such as ransomware attacks. A significant cyber incident, including system failure, security breach, disruption by malware or other damage, could interrupt or delay our operations, result in a violation of applicable cybersecurity and privacy and other laws, damage our reputation, cause a loss of customers or expose sensitive customer data, or give rise to monetary fines and other penalties, which could be significant.
Source: Item 1A, 10-K 0001104659-26-036286 vs Item 1A, 10-K 0001410578-25-000743
MD&A 133 words changed in this paragraph; it is 36% similar to last year's version.
The continuing worldwide implications of the war between Russia and Ukraine and the conflict in the Middle East remain difficult to predict at this time. The imposition These events, such as the interruption in telecommunications or internet services, cyber-related terrorist acts, civil disturbances, war or other catastrophes, could also negatively affect the digital asset economy in one or more jurisdictions. Moreover, foreign laws, regulations or directives may conflict with those of sanctions on Russia by the United States and other countries may negatively impact the acceptance of one or more digital assets by users, merchants and counter sanctions by Russia, service providers outside the United States and may therefore impede the resulting economic impacts on oil prices and other materials and goods, could affect growth or sustainability of the price of materials used digital asset economy in the manufacture of our product candidates. If the price of materials used in the manufacturing of our product candidates increase, that would adversely affect our business United States and the results of our operations. globally.
Source: Item 7, 10-K 0001104659-26-036286 vs Item 7, 10-K 0001410578-25-000743
Legal Proceedings 4 words changed in this paragraph; it is 95% similar to last year's version.
For the Years Ending Minimum December 31, Minimum Lease Payments 2025 2026 $ 675,400 2026 560,996 2027 214,618 214,619 Total future minimum lease payments 1,451,014 775,615 Less: Imputed imputed interest (158,347) (57,008) Present value of lease liabilities 1,292,667 718,607 Less: current portion (575,163) (512,007) Lease liabilities, non-current portion $ 717,504 206,600
Source: Item 3, via Note 11 – Commitments and Contingencies, 10-K 0001104659-26-036286 vs Item 3, via Note 10 – Commitments and Contingencies, 10-K 0001410578-25-000743
Every change, by type
Sentences and paragraphs of HYPD's Risk Factors and MD&A, 10-K 2026-03-30 against 10-K 2025-04-15.
Each links to the text at sec.gov.
Quiet changes are sentences kept from last year with one to four words changed, at least one of them a hedge, a modal or a qualifier
(may, could, will, not, significant, material…). A year or date rolling forward is not counted.
The full word list
adverse, adversely, all, although, anticipate, anticipates, any, approximately, believe, believes, can, cannot, certain, could, expect, expects, generally, however, if, intend, intends, largely, likely, many, material, materially, may, might, most, must, never, no, not, possible, primarily, probable, should, significant, significantly, some, substantial, substantially, unlikely, will, would
AddedRisk Factors
The Hyperliquid platform and technologies and HYPE have a limited operating history.
Read it in 10-K 2026-03-30 at sec.gov ↗
AddedRisk Factors
The Hyperliquid blockchain, exchange and related products launched in early 2023, and the HYPE token launched in November 2024. When we refer to HYPE, we are referring to HYPE tokens and liquid staking tokens derived from HYPE tokens (“LSTs”). We also hold other digital assets. Hyperliquid is an early-stage project with a limited operating history. Developers, validators, traders and market makers may not adopt Hyperliquid’s technology, and we believe that Hyperliquid’s adoption will likely depend on significant platform and product development and differentiation in a highly competitive market. A failure to scale, unexpected technical flaws, privacy issues or the lack of engagement could materially reduce demand for HYPE and adversely affect its value.
Read it in 10-K 2026-03-30 at sec.gov ↗
AddedRisk Factors
Because our treasury strategy is currently primarily focused on holdings of HYPE, our treasury assets are highly dependent upon the value and performance of the Hyperliquid platform and HYPE. If the Hyperliquid platform fails to achieve its objective, or has significant setbacks or delays, the value of HYPE may severely decline, which could materially and adversely impact the value of our treasury assets, liquidity, and financial condition, which could have a substantial impact on the value of our common stock.
Read it in 10-K 2026-03-30 at sec.gov ↗
AddedRisk Factors
HYPE is subject to extreme price volatility, and any sustained decline in the market price of HYPE could lead to substantial losses on our digital asset holdings and could adversely affect the market price of our common stock.
Read it in 10-K 2026-03-30 at sec.gov ↗
AddedRisk Factors
The price of HYPE has exhibited sudden and significant fluctuations due to shifts in market sentiment, speculative trading, macroeconomic trends, technology-related disruptions and regulatory announcements. Because digital asset trading markets are relatively new, largely unregulated and, at times, subject to limited liquidity, HYPE has experienced and may continue to experience larger or more frequent price swings than traditional asset classes. A rapid decrease in the price of HYPE - whether the result of negative perception, a lack of stability on the digital asset trading platforms on which HYPE trades, market manipulation of cryptocurrency trading platforms by customers, a cyber-security incident, regulatory action or other factors-could materially reduce the value of any HYPE we hold, force us to recognize impairment charges, and depress the market price of our securities.
Read it in 10-K 2026-03-30 at sec.gov ↗
AddedRisk Factors
Additionally, large portions of HYPE, potentially 238 million HYPE tokens or more, have been reported to be held by the Hyperliquid core contributors. As a result, trading activity by these parties could have a material impact on the price and trading volume of HYPE. Further, to our knowledge, the core contributors and other large holders of HYPE began to “unlock” their tokens on November 29, 2025, meaning that they became able to sell some of their HYPE starting on such date and at periodic unlock dates over a multi-year period. The large influx of HYPE increases the circulating supply, which can lead to a price drop if demand does not increase proportionally to absorb the new tokens. If all HYPE tokens that were unlocked on that day and are unlocked on subsequent unlock dates are immediately sold, this could have significant impacts on the price of HYPE on or around such unlock dates and depress the price of our common stock.
Read it in 10-K 2026-03-30 at sec.gov ↗
AddedRisk Factors
HYPE is a highly volatile asset, and fluctuations in the price and liquidity of HYPE may influence our financial results and the market price of our listed securities.
Read it in 10-K 2026-03-30 at sec.gov ↗
AddedRisk Factors
Our financial results and the market price of our listed securities would be adversely affected, and our business and financial condition would be negatively impacted, if the price of HYPE decreased substantially, including as a result of:
Read it in 10-K 2026-03-30 at sec.gov ↗
AddedRisk Factors
decreased user and investor confidence in HYPE, including due to the various factors described in this filing;
Read it in 10-K 2026-03-30 at sec.gov ↗
AddedRisk Factors
investment and trading activities such as (i) trading activities of highly active retail and institutional users, speculators and investors or (ii) actual or expected significant dispositions of HYPE by large holders, including the expected liquidation of digital assets seized by governments or associated with entities that have filed for bankruptcy protection, or associated with tokens vested by the Hyperliquid core team;
Read it in 10-K 2026-03-30 at sec.gov ↗
AddedRisk Factors
negative publicity, media or social media coverage, or sentiment due to events in or relating to, or perception of, HYPE, Hyperliquid or the broader digital assets industry;
Read it in 10-K 2026-03-30 at sec.gov ↗
AddedRisk Factors
changes in consumer preferences and the perceived value or prospects of HYPE or the utility of Hyperliquid;
Read it in 10-K 2026-03-30 at sec.gov ↗
RemovedRisk Factors
Significant Accounting Policies - Liquidity and Going Concern of our financial statements included within this Annual Report on Form 10-K.
Read it in 10-K 2025-04-15 at sec.gov ↗
RemovedRisk Factors
Our ongoing exploration of alternative strategic paths may not result in entering into or completing transactions when necessary, and the process of reviewing alternative strategic paths or their conclusion could adversely affect our stock price.
Read it in 10-K 2025-04-15 at sec.gov ↗
RemovedRisk Factors
We continue to evaluate strategic paths to provide the resources necessary to commercialize Mydcombi and maximize stockholder value. Potential strategic paths may include partnerships, joint ventures, mergers, acquisitions or licensing transactions, a combination of these, or other strategic transactions. There can be no assurance, however, that our evaluation will result in transactions or other alternatives, even when deemed necessary. There is no set timetable for our strategic process and we do not intend to provide updates unless or until the Board of Directors approves a specific action or otherwise determines that disclosure is appropriate or necessary.
Read it in 10-K 2025-04-15 at sec.gov ↗
RemovedRisk Factors
Any potential transaction would be dependent on a number of factors that may be beyond our control, including, among other things, market conditions, industry trends, the interest of third parties in a potential transaction with us, obtaining stockholder approval, where necessary, and the availability of financing to third parties in a potential transaction with us on reasonable terms. The process of reviewing alternative strategic paths may be time consuming and may involve the dedication of significant resources and may require us to incur significant costs and expenses. It could negatively impact our ability to attract, retain and motivate employees, and expose us to potential litigation in connection with this process or any resulting transaction. If we are unable to effectively manage the process, our financial condition and results of operations could be adversely affected. In addition, speculation regarding any developments related to the review of strategic alternatives and perceived uncertainties related to the future of our Company could cause our stock price to fluctuate significantly. Further, any alternative strategic paths that may be pursued and completed ultimately may not deliver the anticipated benefits or enhance stockholder value. There can be no guarantee that the process of evaluating alternative strategic paths will result in our Company entering into or completing potential transactions within the anticipated timing or at all.
Read it in 10-K 2025-04-15 at sec.gov ↗
RemovedRisk Factors
On December 12, 2024, we received a letter from Nasdaq notifying us that, because the closing bid price for our common stock was below $0.10 per share for 10 consecutive trading days, we were in breach of Listing Rule 5810(c)(3)(A)(iii). On January 31, 2025, we executed an 80-for-1 reverse stock split, following which we were notified by Nasdaq that we had regained compliance with the Minimum Bid Price Rule.
Read it in 10-K 2025-04-15 at sec.gov ↗
RemovedRisk Factors
Nasdaq Listing Rule 5810(c)(3)(A)(iv) states that any listed company that fails to meet the Minimum Bid Price Rule and has effected a reverse stock split over the prior one-year period, or has effected one or more reverse stock splits over the prior two-year period with a cumulative ratio of 250 shares or more to one, will not be eligible for an automatic 180-day grace compliance period and the Nasdaq Listing Qualifications Department is obligated to immediately issue a delisting determination. Therefore, if we were to fall out of compliance with the Minimum Bid Price requirement prior to January 31, 2026, we would not be able to effect a reverse stock split and would immediately be issued a delisting determination.
Read it in 10-K 2025-04-15 at sec.gov ↗
RemovedRisk Factors
Raising additional capital may cause dilution to our existing stockholders, restrict our operations or require us to relinquish rights to our technologies.
Read it in 10-K 2025-04-15 at sec.gov ↗
RemovedRisk Factors
To the extent that we raise additional capital through the sale of equity or convertible debt securities, our investors’ ownership interest will be diluted. Debt financing, if available, may involve agreements that include covenants limiting or restricting our ability to take specific actions, such as incurring additional debt, making capital expenditures or declaring dividends. If we are unable to obtain funding on a timely basis, we may be required to significantly curtail or delay manufacturing and commercialization plans, which would adversely impact potential revenues, results of operations and our financial condition.
Read it in 10-K 2025-04-15 at sec.gov ↗
RemovedRisk Factors
If we raise additional capital through future collaborations, strategic alliances or third-party licensing arrangements, we may have to relinquish valuable rights to our intellectual property, future revenue streams, Mydcombi, Optejet or clobetasol propionate, or grant licenses on terms that might not be favorable to us.
Read it in 10-K 2025-04-15 at sec.gov ↗
RemovedRisk Factors
We have entered into a loan modification agreement with Avenue and, based on our lack of financial liquidity, we cannot guarantee that we will be able to comply with the terms of this agreement, or continue obtaining forbearance if needed.
Read it in 10-K 2025-04-15 at sec.gov ↗
RemovedRisk Factors
As of March 15, 2025, the Company owed $10.2 million in principal and accrued interest under the facility. Amounts outstanding under the facility bear interest at an annual rate equal to the greater of (a) 7.0% and (b) the prime rate as reported in The
Read it in 10-K 2025-04-15 at sec.gov ↗
RemovedRisk Factors
Wall Street Journal plus 4.45% (the “Interest Rate”). The maturity date is November 1, 2025. On November 22, 2024, the Company entered into the First Amendment, pursuant to which Avenue agreed to defer principal and interest payments on amounts outstanding until February 28, 2025.
Read it in 10-K 2025-04-15 at sec.gov ↗
RewordedRisk Factors
As of March December 31, 2025, we had 300,000,000 600,000,000 shares of common stock authorized and 2,830,546 8,680,005 shares of common stock outstanding, 1,363,135 33,820,785 shares of common stock issuable upon exercise of warrants, 56,318 92,075 shares of our common stock issuable upon exercise of options, 5,952,380 of shares issuable upon the conversion of convertible debt and 247,623 1,545,000 shares of common stock issuable upon the vesting and/or delivery of restricted stock units. units (“RSUs”) and 16,307,691 shares of common stock issuable upon conversion of our Series A Non-Voting Convertible Preferred Stock (the “Series A Preferred Stock”).
Read it in 10-K 2026-03-30 at sec.gov ↗
RewordedRisk Factors
The Although we have the ability to liquidate HYPE tokens to fund our operations, any required additional capital we require in order to remain a going concern may not be available on reasonable terms, if at all, due to a variety of factors, including uncertainty about the future direction of the Company, as well as broader volatile conditions in the economy and capital markets, including recent volatility caused by due to inflation, questions about bank stability and other factors.
Read it in 10-K 2026-03-30 at sec.gov ↗
RewordedRisk Factors
Any such security breach or interruption, as well as any action by us or our employees or contractors that might be inconsistent with the rapidly evolving data privacy and security laws and regulations applicable within the United States and elsewhere where we conduct business, States, could result in enforcement actions by U.S. states, states and the U.S. federal government or foreign governments, liability or sanctions under data privacy laws that protect personally identifiable information, government, regulatory penalties, other legal proceedings such as proceedings, including but not limited to private litigation, the incurrence of significant remediation costs, disruptions to our development programs, business operations and collaborations, operations, diversion of management efforts and damage to our reputation, which could harm our business and operations.
Read it in 10-K 2026-03-30 at sec.gov ↗
RewordedRisk Factors
However, we We cannot provide any assurance that the measures we have taken to date and that we intend to implement will be sufficient to remediate the material weaknesses weakness that we have identified, existed as of December 31, 2025 or to will avoid additional material weaknesses from occurring in the future.
Read it in 10-K 2026-03-30 at sec.gov ↗
RewordedRisk Factors
Delisting of our common stock from Nasdaq could prevent us from maintaining an active, liquid and orderly trading market for our common stock and may materially and adversely impact our ability to consummate certain strategic transactions. stock.
Read it in 10-K 2026-03-30 at sec.gov ↗
RewordedRisk Factors
We require significant capital resources in order to continue to operate our business and conduct our exploration of strategic alternatives, and our limited liquidity could materially and adversely affect our business operations. business.
Read it in 10-K 2026-03-30 at sec.gov ↗
RewordedRisk Factors
Also, it is very difficult to project our current monthly cash burn rate given the transitional status of the Company and this estimate may prove inaccurate rate, and we may expend our limited resources sooner. sooner than we anticipate.
Read it in 10-K 2026-03-30 at sec.gov ↗
RewordedRisk Factors
If that were to happen, the market price of our stock could decline and we could be subject to sanctions or investigations by Nasdaq, the SEC or other regulatory authorities.
Read it in 10-K 2026-03-30 at sec.gov ↗
RewordedRisk Factors
Unless we consent to the selection of an alternative forum, our certificate of incorporation provides that the Court of Chancery of the State of Delaware, or the Court Delaware (the “Court of Chancery, Chancery”) will be, to the fullest extent permitted by law, the sole and exclusive forum for any derivative action or proceeding brought on our behalf; any action asserting a claim of breach of fiduciary duty owed by any of our directors, officers or other employees or agent agents to the Company or our stockholders; any action asserting a claim against us arising pursuant to the Delaware General Corporation Law, or DGCL, or our certificate of incorporation or bylaws; any action to enforce or determine the validity of our certificate of incorporation or bylaws; or any action asserting a claim against us that is governed by the internal affairs doctrine.
Read it in 10-K 2026-03-30 at sec.gov ↗
RewordedRisk Factors
In addition, because our Board board of Directors directors is responsible for appointing the members of our management team, these provisions may frustrate or prevent any attempts by our stockholders to replace or remove our current management by making it more difficult for stockholders to replace members of our Board. board of directors (the “Board of Directors” or the “Board”).
Read it in 10-K 2026-03-30 at sec.gov ↗
RewordedRisk Factors
The failure by our management to apply these funds effectively could result in financial losses that could have a material adverse effect on our business, business and cause the price of our common stock to decline and delay the development of our product candidates. decline.
Read it in 10-K 2026-03-30 at sec.gov ↗
RewordedRisk Factors
If we are not able to comply with the requirements of Section 404 of the Sarbanes-Oxley Act in a timely manner, the market price of our stock could decline and we could be subject to sanctions or investigations by Nasdaq, the stock exchange on which our common stock is listed, the SEC, SEC or other regulatory authorities, which would require additional financial and management resources.
Read it in 10-K 2026-03-30 at sec.gov ↗
Quiet changesRisk Factors
Our ability to publicly or privately sell equity securities and the liquidity of our common stock could would be adversely affected if we are delisted from The Nasdaq Capital Market or if we are unable to transfer our listing to another stock market.
Read it in 10-K 2026-03-30 at sec.gov ↗
Quiet changesRisk Factors
The trading market for our common stock will rely, relies, in part, on the research and reports that industry or financial analysts publish about us or our business.
Read it in 10-K 2026-03-30 at sec.gov ↗
Quiet changesRisk Factors
We are therefore entitled to rely on certain reduced disclosure requirements, such as an exemption from providing selected financial data and certain executive compensation information.
Read it in 10-K 2026-03-30 at sec.gov ↗
AddedMD&A
Hyperion DeFi, Inc., formerly known as Eyenovia, Inc., is the first U.S. publicly listed company building a long-term strategic treasury of HYPE in addition to being a pioneering digital ophthalmic technology company. We are working to provide our shareholders with simplified exposure to the Hyperliquid ecosystem, which we believe to be one of the highest revenue-generating blockchains in the world. At the same time, we continue to execute on our planned completion of development and registration of our Optejet ophthalmic microdose mist delivery system.
Read it in 10-K 2026-03-30 at sec.gov ↗
AddedMD&A
On June 20, 2025, we received approximately $50 million in gross proceeds in connection with the closing of a private placement (the “Private Placement”). Pursuant to the Securities Purchase Agreement, dated as of June 17, 2025, in the Private Placement, the purchasers purchased an aggregate of 5,128,205 shares of the Series A Preferred Stock and warrants to purchase up to 30,769,230 shares of common stock at an exercise price of $3.25 per share. We used the net proceeds from the Private Placement to build a reserve of HYPE.
Read it in 10-K 2026-03-30 at sec.gov ↗
AddedMD&A
In connection with the Private Placement, we entered into a Registration Rights Agreement (the “Registration Rights Agreement”) with the purchasers, which provided that the Company would register the resale of the shares of common stock issuable upon conversion of the Series A Preferred Stock and exercise of the warrants. The Company filed a registration statement with the SEC pursuant to the Registration Rights Agreement on July 18, 2025.
Read it in 10-K 2026-03-30 at sec.gov ↗
AddedMD&A
Chardan Capital Markets LLC (“Chardan”) acted as placement agent for us in connection with the Private Placement. Pursuant to the Engagement Letter, dated as of June 17, 2025, as compensation for its services, we issued to Chardan 307,692 shares of Series A Preferred Stock (convertible into up to 923,076 shares of common stock) and Placement Agent Warrants to purchase up to 1,846,153 shares of common stock at an exercise price of $3.25 per share.
Read it in 10-K 2026-03-30 at sec.gov ↗
AddedMD&A
On September 24, 2025, we entered into Amendment No. 1 (the “Amendment”) to the Amended and Restated Sales Agreement (the “A&R Sales Agreement”) with Chardan Capital Markets, LLC, with respect to our existing at-the-market offering program. The Amendment increases the aggregate offering amount under the A&R Sales Agreement from $50 million to $100 million.
Read it in 10-K 2026-03-30 at sec.gov ↗
AddedMD&A
On November 14, 2025, the Company entered into a new Sales Agreement with Cantor Fitzgerald & Co. and Chardan Capital Markets with respect to the Company’s at-the-market offering program. The new agreement, among other things, increases the aggregate offering price from $100 million to $500 million and increases the total fees payable to the two sales agents from 3.0% to 4.0%.
Read it in 10-K 2026-03-30 at sec.gov ↗
AddedMD&A
During the years ended December 31, 2025 and 2024, the Company received approximately $39.4 million and $6.0 million in proceeds net of offering costs of $1.3 million and $0.2 million from the sale of 5,607,759 and 70,381 shares of its common stock, respectively.
Read it in 10-K 2026-03-30 at sec.gov ↗
AddedMD&A
On June 17, 2025, the Company and the Lenders entered into the Fourth Amendment to Supplement to the Loan and Security Agreement (the “Fourth Amendment”). The Fourth Amendment, among other things, extended the maturity date of the loans under the Loan and Security Agreement to July 1, 2028; provided for an interest-only period from July 1, 2025 until January 31, 2027; reduced the interest rate on the loans from 12.0% to 8.0%, payable half in cash and half in kind; eliminated the option of the Lenders to convert an aggregate amount of up to $10.0 million of the loans outstanding into shares of common stock; and provided us with the option to prepay debt owed under the Loan and Security Agreement in part. In connection with the Fourth Amendment, we issued to the Lenders warrants to purchase an aggregate of 350,000 shares of common stock at an exercise price of $4.00 per share.
Read it in 10-K 2026-03-30 at sec.gov ↗
AddedMD&A
On April 29, 2025, we received a notice from the Staff of Nasdaq stating that the Company’s stockholders’ equity as reported in the 2024 Form 10-K was below the minimum $2,500,000 required for continued listing under Listing Rule 5550(b)(1) (the “Minimum Equity Requirement”). The Notice had no immediate effect on the listing of the Company’s common stock on the Nasdaq Capital Market. The Company submitted a plan to regain compliance with the Nasdaq Listing Rules. On September 2, 2025, we received notice from the Staff of Nasdaq that the Company was now in compliance with the Nasdaq Listing Rules and that the matter was closed.
Read it in 10-K 2026-03-30 at sec.gov ↗
AddedMD&A
We are a “smaller reporting company” as defined under the Exchange Act. We may take advantage of certain of the scaled disclosures available to smaller reporting companies until the last day of the fiscal year in which (i) the market value of our common stock held by non-affiliates exceeds $250 million as of the end of that year’s second fiscal quarter and our annual revenue exceeds $100 million during such completed fiscal year, or (ii) the market value of our common stock held by non-affiliates exceeds $700 million, regardless of our annual revenue, as of the end of that year’s second fiscal quarter.
Read it in 10-K 2026-03-30 at sec.gov ↗
AddedMD&A
We jointly operate a validator node on the Hyperliquid blockchain network and earn HYPE as rewards and commission income for validating transactions and maintaining network security. These activities include both self-staking (using our own tokens) and providing validation services to third-party delegators. The provision of services related to transaction validation on the Hyperliquid blockchain network (through both staking rewards and commission income) is an output of our ordinary activities.
Read it in 10-K 2026-03-30 at sec.gov ↗
AddedMD&A
We recognize revenue by applying the guidance in ASC 606, Revenue from Contracts with Customers (“ASC 606”). HYPE earned from validator operations, in the form of staking rewards and commission income, are recognized as revenue when we satisfy our performance obligations (i.e., successfully validate blocks or transactions as determined by the protocol). The HYPE earned are non-cash consideration and therefore measured at fair value at the inception of each contract.
Read it in 10-K 2026-03-30 at sec.gov ↗
RemovedMD&A
We are an ophthalmic technology company developing our proprietary Optejet® topical ophthalmic medication dispensing platform. In November 2024, we received a negative clinical trial result in the development of our development-stage drug-device combination product, MicroPine. As a result, we restructured our company to minimize expenses and engaged an investment bank to explore strategic options in order to maximize shareholder value. We have paused the national sales roll-out of our products clobetasol propionate and Mydcombi® until additional funding is obtained. At the same time, we accelerated our development efforts relating to the Optejet in order to potentially increase the value of that asset in any strategic transaction or capital raising activities.
Read it in 10-K 2025-04-15 at sec.gov ↗
RemovedMD&A
The ergonomic and functional design of the Optejet allows for horizontal drug delivery and eliminates the need to tilt the head back or the manual dexterity to squeeze a bottle to administer medications. Drug is delivered in a microscopic array of droplets that is both comfortable and matches the amount of fluid that the front of the eye can hold. The precise delivery of a low-volume columnar spray by the Optejet device helps ensure instillation success while minimizing contamination risk with a non-protruding nozzle and self-closing shutter. In clinical trials, the Optejet has demonstrated that its targeted delivery achieves a high rate of successful administration, with 98% of sprays being accurately delivered upon first attempt compared to the established rate reported with traditional eye drops of approximately 50%.
Read it in 10-K 2025-04-15 at sec.gov ↗
RemovedMD&A
A more physiologically appropriate volume of medication in the range of seven to ten microliters is delivered by the Optejet, which is approximately one-fifth of the 35 to 50 microliter dose typically delivered in a single eye drop. Lower volume of medication exposes the ocular surface to less active ingredient and preservatives, potentially reducing ocular stress and surface damage and improving tolerability. The lower volume also minimizes the potential for drug to enter systemic circulation, with the goal of avoiding some common side effects that are related to overdosing of the eye.
Read it in 10-K 2025-04-15 at sec.gov ↗
RemovedMD&A
We are developing versions of the Optejet with on-board digital technology that records the date and time of each use. These data may be used to provide reminders via Bluetooth to smart devices and to allow healthcare practitioners to monitor usage. This information can then be used by practitioners and health care systems to measure treatment compliance and improve medical decision making. In this way, the Optejet could serve as an extension of the physician’s office by providing information that is not currently possible to collect except through the use of diaries.
Read it in 10-K 2025-04-15 at sec.gov ↗
RemovedMD&A
MicroLine is our investigational pharmacologic treatment for presbyopia, a non-preventable, age-related hardening of the lens, which causes the gradual loss of the eye’s ability to focus on near objects and impairs near visual acuity. We have completed two Phase III studies using our Optejet device. In these studies, patients reported high satisfaction with using the device, and a strong preference over using an eye dropper bottle. Since completing these studies, the market opportunity has markedly deteriorated, and we have chosen to put this program on hold and reallocate our resources towards larger opportunities. When and if the market improves, we have kept open the option to continue development of MicroLine, which would include a meeting with the U.S. Food and Drug Administration (the “FDA”) to review our clinical data to date.
Read it in 10-K 2025-04-15 at sec.gov ↗
RemovedMD&A
Our first product using the Optejet technology, Mydcombi®, is the only FDA-approved fixed combination of the two leading mydriatic agents, tropicamide and phenylephrine, in the United States. As an ophthalmic spray delivered with Optejet technology, Mydcombi may present a number of benefits for ophthalmic surgical centers, optometric and ophthalmic offices and patients. Those benefits may include improved cost-effectiveness in centers that employ single-use bottles for mydriasis, more efficient use of office time and resources, and an overall improved doctor-patient experience.
Read it in 10-K 2025-04-15 at sec.gov ↗
RemovedMD&A
The first commercial sale of Mydcombi occurred on August 3, 2023 as part of a targeted launch. On July 24, 2024, we received written comments from the FDA providing direction for the design of a clinical bridging study to transition Mydcombi into our new Gen-2 Optejet device, which has a significantly lower cost to manufacture than the currently approved product.
Read it in 10-K 2025-04-15 at sec.gov ↗
RemovedMD&A
On August 10, 2020, we entered into a license agreement with Arctic Vision (as amended on September 14, 2021, the “Arctic Vision License Agreement”) pursuant to which Arctic Vision may develop and commercialize MicroPine (Eyenovia’s proprietary drug-device combination of low-dose atropine and the Optejet platform), MicroLine and Mydcombi in Greater China (mainland China, Hong Kong, Macau and Taiwan) and South Korea. Under the terms of the Arctic Vision License Agreement, as amended, we received an upfront payment of $4.25 million before any payments to Senju Pharmaceutical Co., Ltd. (“Senju”).
Read it in 10-K 2025-04-15 at sec.gov ↗
RemovedMD&A
On October 9, 2020, we entered into a license agreement (the “Bausch License Agreement”) with Bausch + Lomb (“B+L”), pursuant to which B+L had the rights to develop and commercialize MicroPine in the United States and Canada. Under the terms of the Bausch License Agreement, we received an upfront payment of $10.0 million and we were eligible to receive up to a total of $35.0 million in additional payments, based on the achievement of certain regulatory and launch-based milestones. B+L also agreed to pay royalties to Eyenovia on a tiered basis (ranging from mid-single digit to mid-teen percentages) on gross profits from sales of MicroPine in the United States and Canada, subject to certain adjustments. Under the terms of the Bausch License Agreement, B+L assumed sponsorship of the IND as well as ownership and the costs related to the ongoing CHAPERONE study, which was a Phase III efficacy and safety trial of MicroPine.
Read it in 10-K 2025-04-15 at sec.gov ↗
RemovedMD&A
On January 12, 2024, we entered into a subsequent agreement with B+L to repatriate our rights to MicroPine and take control of the CHAPERONE study. In this agreement, we agreed to pay B+L $2 million in cash and an additional $3 million in common stock upon successful transfer of the regulatory documents and study elements to Eyenovia. We also agreed to pay B+L a 2% royalty on net sales once MicroPine is commercialized in the United States, assuming receipt of regulatory approvals. We believed that this revised arrangement was in our and our shareholders’ best interests, as it could have substantially increased the value of the asset through potential improvements in the conduct of the study, including a planned interim analysis of the data in late 2024.
Read it in 10-K 2025-04-15 at sec.gov ↗
RemovedMD&A
On September 26, 2024, we announced the U.S. launch and commercial availability of clobetasol propionate ophthalmic suspension 0.05%.
Read it in 10-K 2025-04-15 at sec.gov ↗
RemovedMD&A
On November 15, 2024, we announced the outcome of an independent review of the clinical results of the three-year efficacy and safety data from the MicroPine Phase III CHAPERONE study conducted by a Data Monitoring Committee (“DMC”). The DMC, made up of independent ophthalmologists and optometrists who specialize in pediatric myopia as well as a statistician, reviewed the safety and efficacy data from all evaluable patients. After the completion of three-year therapy for myopia with MicroPine, statistical superiority was not observed and was deemed unlikely to occur in at least one of the active dose arms compared with placebo, which was the primary efficacy endpoint of the trial. There were no safety issues or serious adverse events identified. As a result of this finding, we closed out the CHAPERONE study and put the project on hold in December 2024.
Read it in 10-K 2025-04-15 at sec.gov ↗
RewordedMD&A
During the next twelve months we have commitments to pay (a) $5.5 $2.2 million to settle our December 31, 2024 2025 accounts payable, accrued expenses and other current liabilities, liabilities and (b) $0.6 $0.5 million relating to our non-cancelable operating lease commitments, and (c) $10.7 million of gross payments due under our notes payable and convertible notes payable (if not previously converted). commitments.
Read it in 10-K 2026-03-30 at sec.gov ↗
RewordedMD&A
The Reacquisition of license rights for the year ended December 31, 2024 totaled $4.9 million is million, comprised of the aggregate $5.0 million of payments ($2.0 million of cash and $3.0 million settled in common stock) to B+L Bausch + Lomb in connection with the reacquisition of the Bausch Licensed Product (which we are recording as an operating expense), partially offset by $0.1 million allocated to the repurchase of equipment.
Read it in 10-K 2026-03-30 at sec.gov ↗
RewordedMD&A
Research In 2024, prior to the termination of our CHAPERONE study, our research and development expenses are were incurred in connection with the research and development of our prior Optejet microdose therapeutics and consist consisted primarily of contract service expenses.
Read it in 10-K 2026-03-30 at sec.gov ↗
RewordedMD&A
Research and development expenses for the year ended December 31, 2024 2025 totaled $14.5 $1.9 million, an increase a decrease of $1.5 $12.6 million, or 11.5%, 87%, as compared to $13.0 $14.5 million recorded for the year ended December 31, 2023. 2024.
Read it in 10-K 2026-03-30 at sec.gov ↗
RewordedMD&A
Revenue for the year ended December 31, 2023 2024 totaled $3,787, $57,336, which was offset by cost of revenues of $16,005. $3,927,228, both of which were entirely from ophthalmic technology.
Read it in 10-K 2026-03-30 at sec.gov ↗
RewordedMD&A
Asset impairments expense for the year ended December 31, 2024 was approximately $11.2 million, compared to no expense for the year ended December 31, 2023. million.
Read it in 10-K 2026-03-30 at sec.gov ↗
RewordedMD&A
After the next twelve months we have commitments to pay (a) $0.7 $0.2 million relating to our non-cancelable operating lease commitments. commitments and (b) $8.3 million relating to our notes payable.
Read it in 10-K 2026-03-30 at sec.gov ↗
RewordedMD&A
Selling, general and administrative expenses for the year ended December 31, 2024 2025 totaled $14.3 $17.2 million, an increase of $1.9 $2.8 million, or 15.0%, 20%, as compared to $12.4 $14.3 million recorded for the year ended December 31, 2023. 2024.
Read it in 10-K 2026-03-30 at sec.gov ↗
RewordedMD&A
As of December 31, 2024, 2025, we had a cash and cash equivalents balance of $2.1 $6.4 million, a working capital deficit surplus of approximately $13.1 $4.5 million and stockholders’ deficiency equity of $12.7 $41.1 million.
Read it in 10-K 2026-03-30 at sec.gov ↗
RewordedMD&A
Our net losses were $49.8 $45.3 million and $27.3 $49.8 million for the years ended December 31, 2024 2025 and 2023. 2024, respectively.
Read it in 10-K 2026-03-30 at sec.gov ↗
RewordedMD&A
Total other expense for the year ended December 31, 2024 primarily consisted of approximately $2.5 million of interest expense related to the Avenue loan, Loan, partially offset by $1.2 million of changes in fair value of equity consideration (the equity payable for the B+L Bausch + Lomb and Formosa transactions) Pharmaceuticals) and approximately $0.2 million of interest income, primarily from Treasury bills.
Read it in 10-K 2026-03-30 at sec.gov ↗
RewordedMD&A
(i) the accounting estimate requires us to make assumptions about matters that were highly uncertain at the time the accounting estimate was made, and (ii) changes in the estimate that are reasonably likely to occur from period to period or use of different estimates that we reasonably could have used in the current period, would have a material impact on our financial condition or results of operations.
Read it in 10-K 2026-03-30 at sec.gov ↗