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EyePoint Pharmaceuticals announced that the first patient has been dosed in the Phase 1 clinical trial of EYP-1901 as a potential twice-yearly sustained delivery anti-VEGF treatment targeting wet age-related macular degeneration (wet AMD).
EyePoint Pharmaceuticals announced positive results from its good laboratory practice (GLP) preclinical toxicology study of EYP-1901, a potential six-month sustained delivery intravitreal anti-VEGF treatment using its proprietary bioerodible Durasert® ...
EyePoint Pharmaceuticals announced positive topline 36-month follow-up data from the second Phase 3 trial of YUTIQ® (fluocinolone acetonide intravitreal implant) 0.18 mg three-year micro-insert ...