Press Releases April 7, 2026

Oculis to Participate in Upcoming Investor Conferences

Oculis Announces Participation in Investor Conferences and Promises 2026 as Landmark Year with Multiple Clinical Trial Readouts

By Nina Shah OCS
Oculis to Participate in Upcoming Investor Conferences
OCS

Oculis Holding AG will participate in prominent investor conferences in April 2026, highlighting advancements in its late-stage ophthalmic and neuro-ophthalmic pipeline. Key upcoming milestones include Phase 3 pivotal results for OCS-01 in diabetic macular edema expected in June 2026, and late 2026 topline results for Licaminlimab in dry eye disease. The company’s Privosegtor candidate has received FDA Breakthrough Therapy and EMA PRIME designations for optic neuritis, reflecting significant market potential. With a solid financial position, Oculis aims to deliver six pivotal clinical readouts this year, driving its transformation into a leader in neuro-ophthalmology and ophthalmology.

Key Points

  • Oculis plans multiple pivotal clinical trial readouts in 2026, including Phase 3 results for OCS-01 and registrational data for Licaminlimab.
  • Privosegtor granted FDA Breakthrough Therapy and EMA PRIME designations, targeting a market opportunity exceeding $7 billion in the U.S.
  • Company participation in virtual and European investor conferences to update stakeholders on its innovative neuro-ophthalmic pipeline.

ZUG, Switzerland, April 07, 2026 (GLOBE NEWSWIRE) -- Oculis Holding AG (Nasdaq: OCS; XICE: OCS) (“Oculis” or the “Company”), a global biopharmaceutical company focused on innovations addressing ophthalmic and neuro-ophthalmic diseases with significant unmet medical needs, announced today that Oculis’ management will participate in upcoming investor conferences in April.

Oculis is pleased to present updates of its innovative, highly differentiated, late-stage portfolio. 2026 promises to be a landmark year for the company in its transformation into a leader in neuro-ophthalmology and ophthalmology. Key highlights include: OCS-01 (DIAMOND Phase 3 trials) topline pivotal results in diabetic macular edema (DME) on track for June 2026; Licaminlimab (PREDICT-1 registrational trial) being evaluated as the first genotype-based development program to drive precision medicine in dry eye disease (DED) with topline results planned around late 2026; Privosegtor (PIONEER program) granted Breakthrough Therapy designation by the U.S. Food and Drug Administration (FDA) and Priority Medicines (PRIME) designation by the European Medicines Agency (EMA) for optic neuritis (ON) as Oculis advances the registrational program in two optic neuropathies to address a potential market opportunity of $7B+ in the U.S. alone.

With a strong balance sheet and robust pipeline, Oculis is well-positioned to deliver 6 pivotal readouts with the current funding, to fulfil its mission to save sight and improve eye care with groundbreaking treatments.

Needham Healthcare Conference
April 13-16, Virtual
Company presentation on April 14, 9:30 AM ET
Webcast link: Register here

Van Lanschot Kempen Life Sciences Conference
April 15-16, Amsterdam, Netherlands
Oculis management will participate in one-on-one meetings.

The Company will be available for one-on-one meetings during the conferences. Interested investors should contact their respective representative at the sponsoring institutions to request meetings.

Webcast links, when available, are posted to the Oculis website on the Events & Presentation page under the Investors & Media section.

-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 Contacts
Ms. Sylvia Cheung, CFO
[email protected]

Investor Relations
LifeSci Advisors
Corey Davis, Ph.D.
[email protected]

Media Relations
ICR Healthcare
Amber Fennell / David Daley / Sean Leous
[email protected]

Cautionary Statement Regarding Forward Looking Statements

This press release contains forward-looking statements and information. For example, statements regarding the development plans for Privosegtor, OCS-01, and Licaminlimab; the initiation, timing, progress and results of clinical trials of Privosegtor, OCS-01, and Licaminlimab; and Oculis’ research and development programs, regulatory and business strategy, future development plans, market opportunity 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 U.S. Securities and Exchange Commission (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.


Risks

  • Clinical trial outcomes for OCS-01, Licaminlimab, and Privosegtor remain uncertain and may not meet expected efficacy or safety endpoints.
  • Regulatory approvals in multiple jurisdictions depend on clinical data which can be subject to delays or unfavorable review.
  • Market adoption of new ophthalmic and neuro-ophthalmic therapies faces competition and reimbursement challenges, impacting commercial success.

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