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
oculis.comLast updated
In short: Oculis shifted its focus to neuro-ophthalmology following a Phase 3 trial failure, while advancing its Privosegtor and Licaminlimab assets.
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.
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...
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Biotech company Oculis will acquire all worldwide development and commercial rights to Privosegtor, one of its two core product candidates, from Accure. This acquisition will...
Oculis Holding AG (OCS) delivered earnings and revenue surprises of +58.33% and +49.05%,...
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