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Oculis Holding AG Ordinary shares

Oculis Holding AG is a clinical-stage biopharmaceutical company that develops drug candidates for ophthalmic, neuro-ophthalmic, and neurological diseases. Its lead candidates include OCS-01, a topical dexamethasone optireach formulation in Phase 3 trials for diabetic macular edema; OCS-02, a topical biologic in Phase 2b trials for dry eye disease; and OCS-05, a disease-modifying neuroprotective agent for neurological damage with indications for glaucoma, dry age-related macular degeneration, diabetic retinopathy, and acute optic neuritis. The company was formerly known as Oculis SA and changed its name to Oculis Holding AG in March 2023. Founded in 2017, it is based in Zug, Switzerland.

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Oculis Director Lionel Carnot Resigns From Board After Nearly a Decade

Oculis Holding AG announced that director Lionel Carnot is resigning from its Board of Directors, effective today, after nearly a decade of service since 2017. The company said the departure is purely a personal decision and not the result of any disagreement with Oculis on any matter relating to its operations, policies, or practices. Following the resignation, the Board will consist of eight members, and the Remuneration Committee, which Carnot chaired, will be led by Geraldine O'Keeffe as chair with Gregory Perry and Robert Warner as members. Board Chair Anthony Rosenberg credited Carnot with guiding Oculis through its evolution from a private startup to a publicly listed late-stage biopharmaceutical company, while Carnot said he remains confident in the company's pipeline as an investor. Under Swiss law, the vacancy may only be filled at a future annual or special general meeting, and Oculis said it will begin identifying a successor and provide updates as appropriate.
OCS · · Neutral Director Lionel Carnot resigns from Oculis board after nearly a decade; company says it is a personal decision with no disagreement, a governance change with no clear directional impact.
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Biotech & Genomic Medicine▲

Oculis to acquire full rights to Privosegtor from Accure Therapeutics

Oculis Holding AG has signed an asset purchase agreement to acquire all worldwide development and commercial rights to its lead neuro-ophthalmology candidate Privosegtor from Accure Therapeutics. The deal terminates Oculis’ existing license agreement with Accure, eliminating associated milestone payments and royalties while securing greater economic upside. Total consideration includes a $3.8 million upfront cash payment and up to 2,050,000 Oculis ordinary shares, consisting of upfront shares subject to a two-year lockup and earnout shares tied to development and regulatory milestones. The transaction also covers an early-stage preclinical neurology candidate, ACT-02, in a separate closing. The Privosegtor closing is expected by February 28, 2027, and the ACT-02 closing by March 31, 2027.
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Biotech & Genomic Medicine › Neuroscience & Neurodegenerative Competition
OCS · Capital · Positive Oculis acquires full rights to Privosegtor, eliminating milestone payments and royalties, securing greater economic upside.
Accure Therapeutics, S.L. · Capital · Positive Accure receives upfront cash and shares, plus earnout shares tied to milestones, monetizing its asset.
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Oculis reports $282.3 million cash position and advances neuro-ophthalmology pivot

Oculis Holding AG reported cash, cash equivalents, and short-term investments of $282.3 million as of June 30, 2026, providing a cash runway into the second half of 2029. The company is advancing its pivot to neuro-ophthalmology with Privosegtor as the lead late-stage asset, progressing site activations in the PIONEER-1 registrational trial for optic neuritis and receiving positive FDA pre-IND feedback to expand into acute multiple sclerosis relapses, with an IND submission planned for the fourth quarter of 2026. Enrollment in the PREDICT-1 genotype-based registrational trial of Licaminlimab in dry eye disease is proceeding as planned, with all sites activated and over 45% of patients randomized, and topline results are expected around year-end. Following the DIAMOND topline results in May, Oculis does not plan to pursue an FDA regulatory filing for OCS-01 in diabetic macular edema. The company will host an R&D Day in the fourth quarter to share updates on Privosegtor's clinical development.
OCS · Capital · Positive Reports strong cash position and advances neuro-ophthalmology pipeline with positive FDA feedback
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Biotech & Genomic Medicine▲

Oculis Gets Positive FDA Feedback for Privosegtor in Acute MS Relapses

Oculis Holding AG announced positive FDA pre-IND feedback supporting a regulatory pathway for Privosegtor in acute multiple sclerosis relapses. The FDA Division of Neurology confirmed that existing Privosegtor data can be cross-referenced for a new Investigational New Drug application, which Oculis plans to submit in the fourth quarter of 2026. The company also intends to host an R&D Day in the fourth quarter of 2026 to detail the pivotal development program for Privosegtor in acute MS relapses and provide an update on the PIONEER program in optic neuropathies. In pre-market trading on NasdaqGM, Oculis shares rose 4.97 percent to $11.87.
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Biotech & Genomic Medicine › Neuroscience & Neurodegenerative ▲Regulation
OCS · Regulation · Positive FDA positive pre-IND feedback supports regulatory pathway for Privosegtor in acute MS relapses.
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Schall Law Firm Investigates Oculis Holding AG Over Failed Phase 3 Trials

The Schall Law Firm has launched an investigation into Oculis Holding AG for potential securities law violations. The investigation centers on whether the company made false or misleading statements about its Phase 3 DIAMOND trials, which Oculis had claimed were advancing as planned. On May 29, 2026, the company announced that both DIAMOND trials failed to meet their primary endpoints and that it would not pursue an FDA filing for its drug candidate. Investors who suffered losses are encouraged to contact the firm.
OCS · Regulation · Negative Investigation into potential securities law violations and failed Phase 3 trials leading to no FDA filing.
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