EyePoint Announces Topline Results from LUCIA, the Second Pivotal Phase 3 Clinical Trial of DURAVYU™ in Wet AMD

- LUCIA did not achieve the primary endpoint of statistical non-inferiority in mean change in BCVA versus on-label aflibercept control, despite demonstrating visual improvement- - Key secondary endpoints in LUCIA were met including a superior 38% reduction in treatment burden (nominal p-value - - Continued favorable safety profile for DURAVYU with redosing - ─ DME program remains on track with pivotal Phase 3 topline data from two identical clinical trials anticipated in Q4 2027 - - Conference call to discuss the results to be held today at 8:00 a.m. EDT - WATERTOWN, Mass., Oct. 19, 2026 (GLOB
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