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Oculis Reports Q4 and Full Year 2025 Financial Results and Provides Company Update

Key Takeaway: Oculis Holding AG reported strong financial results for Q4 and full year 2025, highlighting significant clinical advancements, particularly with Privosegtor, which received FDA Breakthrough Therapy designation. The company anticipates major milestones in 2026, including trial results for OCS-01 and Licaminlimab. Despite increased operating losses, Oculis's cash reserves have grown substantially, positioning it well for future developments.
Price reaction · baseline $27.57 (2026-03-03 close) · hit pre-market · 3 other OCS headline(s) in the window, move may be shared
day 0 close · peak
+0.5%

Market Sentiment Analysis

POSITIVE FACTORS

  • Significant clinical progress in late-stage portfolio.
  • Privosegtor received FDA Breakthrough Therapy designation.
  • Strong financial position with increased cash reserves.
  • Upcoming major registrational milestones in 2026.

CONCERNS & RISKS

  • Year-to-date net loss increased compared to 2024.
  • Operating expenses driven by clinical trials are rising.
  • Foreign exchange revaluation losses impacted financials.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+32%
120-day peak, hindsight
Typical move
3.8%
average across 4 past catalysts
Lead asset
Privosegtor
Phase 3 · Optic Neuritis

Full Press Release Details

ZUG, Switzerland, March 3, 2026 -- Oculis Holding AG (Nasdaq: OCS / XICE: OCS) (Oculis), a global biopharmaceutical company focused on breakthrough innovations to address significant unmet medical needs in ophthalmology and neuro-ophthalmology, today announced results for the fourth quarter and full year ended December 31, 2025, and provided an overview of the Company’s progress.
Riad Sherif, M.D., Chief Executive Officer of Oculis, stated“Oculis has delivered a transformative 2025, marked by significant clinical progress across our late-stage portfolio and a strategic expansion into neuro-ophthalmology. The compelling Phase 2 ACUITY results for Privosegtor in optic neuritis led to a pivotal FDA Breakthrough Therapy designation and anchored the launch of our global PIONEER registrational program. We believe Privosegtor holds immense potential as a first-in-class neuroprotective platform for a range of neuro-axonal diseases. 2026 is positioned to be a landmark year for the company with a roadmap featuring three major expected registrational milestones: the DIAMOND-1 and DIAMOND-2 trials readout with OCS-01, a potential first-in-class eye drop in DME, anticipated in Q2, the PREDICT-1 trial results for Licaminlimab with a precision medicine approach in dry eye disease planned in Q4, and the commencement of three registrational trials with Privosegtor as part of the PIONEER program. The operational excellence and significant milestones we achieved in 2025 have uniquely positioned Oculis to drive innovation in areas of high unmet medical need, a potential market opportunity of over $30 billion, with the aim of redefining the standard of care in ophthalmology and neuro-ophthalmology.”
Recent Clinical Highlights and Upcoming Milestones:
Privosegtor:
OCS-01:
Licaminlimab:
Q4 and Full Year 2025 Financial Highlights:
As of December 31, 2025, Oculis held cash, cash equivalents and short-term investments of CHF 213.0 million or $268.7 million, compared to CHF 98.7 million or $109.0 million as of December 31, 2024. The increase in cash, cash equivalents and short-term investments was primarily due to equity financings closed in February and November 2025 for aggregate gross proceeds of $210.0 million (CHF 178.9 million). Research and development expenses were CHF 13.3 million or $16.6 million for the three months ended December 31, 2025, compared to CHF 11.8 million or $13.4 million in the same period in 2024. The increase was primarily due to advancements in clinical development activities of our late-stage portfolio and associated personnel expenses. General and administrative expenses were CHF 7.8 million or $9.7 million for the three months ended December 31, 2025, compared to CHF 5.5 million or $6.3 million in the same period in 2024. The increase was primarily driven by personnel expenses and external professional services costs. Year-to-date net loss was CHF 99.0 million or $119.1 million for the year ended December 31, 2025, compared to CHF 85.8 million or $97.4 million for the same period in 2024. The increase was primarily due to an increase in operating expenses driven by the OCS-01 Phase 3 DIAMOND trials, increased personnel costs and a CHF 7.4 million or $8.9 million increase in foreign exchange revaluation loss, offset by a CHF 3.2 million or $3.9 million decrease in the non-cash fair value adjustment on warrant liabilities resulting from warrant exercises during the year offset by increases in the fair value of outstanding warrants.
Upcoming Events:
Medical Conferences and Industry Events
Investor Conferences
Consolidated Statements of Financial Position (Unaudited)
(Amounts in CHF thousands) As of December 31, As of December 31,
2025 2024
ASSETS
Non-current assets
Property and equipment 534 385
Intangible assets 13,292 13,292
Right-of-use assets 2,463 1,303
Other non-current assets 785 476
Total non-current assets 17,074 15,456
Current assets
Other current assets 4,883 5,605
Accrued income 993 629
Short-term financial assets 131,684 70,955
Cash and cash equivalents 81,329 27,708
Total current assets 218,889 104,897
TOTAL ASSETS 235,963 120,353
EQUITY AND LIABILITIES
Shareholders' equity
Share capital 587 446
Share premium 551,731 344,946
Reserve for share-based payment 30,387 16,062
Actuarial loss on post-employment benefit obligations (1,634 ) (2,233 )
Treasury shares (7 ) (10 )
Cumulative translation adjustments (480 ) (271 )
Accumulated losses (384,514 ) (285,557 )
Total equity 196,070 73,383
Non-current liabilities
Long-term lease liabilities 1,811 865
Defined benefit pension liabilities 1,335 1,870
Total non-current liabilities 3,146 2,735
Current liabilities
Trade payables 1,800 5,871
Accrued expenses and other payables 19,967 18,198
Short-term lease liabilities 502 315
Warrant liabilities 14,478 19,851
Total current liabilities 36,747 44,235
Total liabilities 39,893 46,970
TOTAL EQUITY AND LIABILITIES 235,963 120,353
Consolidated Statements of Loss (Unaudited)
(Amounts in CHF thousands,except per share data) For the three monthsended December 31, For the twelve monthsended December 31,
2025 2024 2025 2024
Grant income 411 3 1,199 686
Operating income 411 3 1,199 686
Research and development expenses (13,288) (11,763) (57,085) (52,083)
General and administrative expenses (7,756) (5,500) (25,786) (21,807)
Operating expenses (21,044) (17,263) (82,871) (73,890)
Operating loss (20,633) (17,260) (81,672) (73,204)
Finance income 319 371 1,770 2,168
Finance expense (241) (247) (833) (639)
Fair value adjustment on warrant liabilities (3,238) (13,387) (12,294) (15,531)
Foreign currency exchange gain (loss) 97 1,630 (6,114) 1,269
Finance result (3,063) (11,633) (17,471) (12,733)
Loss before tax for the period (23,696) (28,893) (99,143) (85,937)
Income tax benefit (expense) 182 238 186 160
Loss for the period (23,514) (28,655) (98,957) (85,777)
Loss per share:
Basic and diluted loss attributable to equity holders (0.42) (0.67) (1.89) (2.12)
- ENDS-
About Oculis
Oculis is a global biopharmaceutical company (Nasdaq: OCS; XICE: OCS) focused on breakthrough innovations to address significant unmet medical needs in neuro-ophthalmology and ophthalmology. Oculis’ highly differentiated late-stage clinical pipeline includes three core product candidates: Privosegtor, a breakthrough neuroprotective candidate in the PIONEER program which consists of studies intended to support registration plans for treatment in optic neuropathies like optic neuritis (ON) and non-arteritic anterior ischemic optic neuropathy (NAION), with potentially broad clinical applications in various other neuro-ophthalmic and neurological diseases; OCS-01, an eye drop in pivotal registration studies, aiming to become the first non-invasive topical treatment for diabetic macular edema (DME); and Licaminlimab, a novel, topical anti-TNFα in registrational trial, which is being developed with a genotype-based approach to drive precision medicine in dry eye disease (DED). Headquartered in Switzerland with operations in the U.S. and Iceland, Oculis is led by an experienced management team with a successful track record and supported by leading international healthcare investors.
For more information, please visit:www.oculis.com
Oculis ContactMs. Sylvia Cheung, CFOsylvia.cheung@oculis.com
Investor RelationsLifeSci AdvisorsCorey Davis, Ph.D.cdavis@lifesciadvisors.com
Media RelationsICR HealthcareAmber Fennell / David Daley / Sean Leousoculis@icrhealthcare.com
Cautionary Statement Regarding Forward Looking Statements
This press release contains forward-looking statements and information. For example, statements regarding the potential benefits of the Company’s product candidates, the initiation, timing, progress and results of current and future clinical trials, Oculis’ research and development programs, regulatory and business strategy; Oculis’ future development plans; the timing or likelihood of regulatory filings and approvals; statements about market opportunity, and the Company’s expected financial position and cash runway, are forward-looking. All forward-looking statements are based on estimates and assumptions that, while considered reasonable by Oculis and its management, are inherently uncertain and are inherently subject to risks, variability, and contingencies, many of which are beyond Oculis’ control. These forward-looking statements are provided for illustrative purposes only and are not intended to serve as, and must not be relied on by an investor as, a guarantee, assurance, prediction or definitive statement of a fact or probability. Actual events and circumstances are difficult or impossible to predict and will differ from assumptions. All forward-looking statements are subject to risks, uncertainties and other factors that may cause actual results to differ materially from those that we expected and/or those expressed or implied by such forward-looking statements. Forward-looking statements are subject to numerous conditions, many of which are beyond the control of Oculis, including those set forth in the Risk Factors section of Oculis’ annual report on Form 20-F and any other documents filed with the SEC. Copies of these documents are available on the SEC’s website, www.sec.gov. Oculis undertakes no obligation to update these statements for revisions or changes after the date of this release, except as required by law.
References:

Frequently Asked Questions

What were Oculis's financial results for Q4 2025?

Oculis reported a net loss of CHF 99.0 million for the year, up from CHF 85.8 million in 2024.

What is the significance of Privosegtor for Oculis?

Privosegtor received FDA Breakthrough Therapy designation and is part of the PIONEER program.

What are the upcoming milestones for Oculis in 2026?

Oculis plans to report results for OCS-01 and Licaminlimab, and start trials for Privosegtor.

How did Oculis's cash position change in 2025?

Oculis's cash reserves increased to CHF 213.0 million, up from CHF 98.7 million in 2024.

What are the main areas of focus for Oculis?

Oculis focuses on innovations in ophthalmology and neuro-ophthalmology, addressing unmet needs.

Last updated: Mar 4, 2026