Oculis begins treating first patient in PIONEER-1 trial
FDA granted Special Protocol Assessment for Privosegtor. This follows positive Phase 2 ACUITY data towards a first-in-class optic neuritis treatment.
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Clinical biopharmaceutical company
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In short: Oculis advanced Privosegtor, completed PREDICT-1 randomization, and reported biomarker data after its OCS-01 trials failed.
FDA granted Special Protocol Assessment for Privosegtor. This follows positive Phase 2 ACUITY data towards a first-in-class optic neuritis treatment.
The transaction includes a $3.8 million upfront payment and share consideration, strengthening Oculis' neuro-ophthalmology pipeline ahead of Phase 3 trials
Cash reserves reach $282.3 million as Privosegtor enters Phase 3 trials while Licaminlimab enrollment exceeds 45%. The company pivots to neuro-ophthalmology with strong balance sheet support.
The FDA supports the regulatory pathway for treating acute multiple sclerosis relapses with Privosegtor. Oculis plans to submit a new Investigational New Drug application in Q4 2026.
Oculis Holding AG has completed randomization in the genotype-based registration study PREDICT-1 on licaminlimab, with the aim of enabling precision medicine for dry eye disease...
Oculis Holding AG remains a clinical-stage biopharma focused on ophthalmic diseases, with a $650M market cap. Click to read my analysis on OCS.
Company pivot to neuro-ophthalmology continues with Privosegtor positioned as lead late-stage asset through the registrational PIONEER program with expansion potential in acute multiple sclerosis (MS...
Please provide your email address to receive an email when new articles are posted on . Oculis will acquire all worldwide rights to privosegtor from...
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