Oculis AG(US:OCS) Globenewswire·2026-01-08 09:00Core Insights - Oculis Holding AG is advancing its late-stage pipeline, particularly focusing on Privosegtor and OCS-01, which address significant unmet medical needs in ophthalmology and neuro-ophthalmology [1][6] Group 1: Privosegtor - Privosegtor has received breakthrough therapy designation from the U.S. FDA for treating optic neuritis, based on positive results from the ACUITY Phase 2 trial [2][10] - In the ACUITY trial, patients receiving Privosegtor showed an average gain of 18 letters in vision improvement compared to placebo, indicating a clinically meaningful two-fold improvement in visual resolution [3] - The PIONEER program has been launched to support registration for Privosegtor in optic neuritis and non-arteritic anterior optic neuropathy (NAION), with a potential market opportunity exceeding $7 billion in the U.S. [4][7] Group 2: OCS-01 - OCS-01 is in Phase 3 development as the first eye drop treatment for diabetic macular edema (DME), targeting a market opportunity of approximately $3 billion in the U.S. [5][15] - The diagnosed DME population in the U.S. is estimated to be around 1.8 million, highlighting the significant unmet medical need for effective treatments [5] - Topline results from the DIAMOND Phase 3 trials for OCS-01 are expected in Q2 2026, with an NDA submission planned for Q4 2026 [5][6] Group 3: Market Potential - The combined market potential for Oculis' neuroprotective therapies and DME treatments could exceed $30 billion, reflecting the substantial unmet needs in these areas [6][10] - The company is positioned to transform treatment landscapes in neuro-axonal diseases and diabetic eye conditions, which currently lack effective therapies [6][15]