Eyepoint Announces Participation At Upcoming Investor Conferences
-    Guggenheim's 2   nd  Annual Healthcare Innovation Conference 
 
Forum: Fireside Chat
Date: Monday, November 10, 2025
Time: 10:30 a.m. ET
-    Stifel 2025 Healthcare Conference 
 
Forum: Corporate Presentation
Date: Wednesday, November 12, 2025
Time: 10:40 a.m. ET
-    Jefferies London Healthcare Conference 
 
Forum: 1x1 Investor Meetings
Date: Monday, November 17, 2025
A live webcast and subsequent archived replay of each presentation may be accessed via the Investors section of the Company website at .
About EyePoint
EyePoint Pharmaceuticals, Inc. (Nasdaq: EYPT) is a clinical-stage biopharmaceutical company committed to developing and commercializing innovative therapeutics to improve the lives of patients with serious retinal diseases. The Company's lead product candidate, DURAVYUTM, is an innovative investigational sustained delivery treatment for serious retinal diseases combining vorolanib, a selective and patent-protected tyrosine kinase inhibitor (TKI), in next-generation bioerodible Durasert ETM technology. Supported by robust safety and efficacy data across multiple clinical trials and indications, DURAVYU is currently being evaluated in two Phase 3 pivotal trials for wet age-related macular degeneration (wet AMD) with data anticipated in mid-2026. First patient dosing in the pivotal Phase 3 clinical trials in diabetic macular edema (DME) is expected in the first quarter of 2026.
The Company is committed to partnering with the retina community to improve patient lives while creating long-term value, with four approved drugs over three decades and tens of thousands of eyes treated with EyePoint innovation.
EyePoint is headquartered in Watertown, Massachusetts, with a commercial manufacturing facility in Northbridge, Massachusetts.
Vorolanib is licensed to EyePoint exclusively by Equinox Sciences, a Betta Pharmaceuticals affiliate, for the localized treatment of all ophthalmic diseases outside of China, Macao, Hong Kong and Taiwan.
DURAVYUTM has been conditionally accepted by the FDA as the proprietary name for EYP-1901 (vorolanib intravitreal insert). DURAVYU is an investigational medicinal product and is not authorized for sale in any country at the present time. FDA approval in the United States and marketing authorization in any other country and the timeline for potential approval or authorization is uncertain.
Investors:
Tanner Kaufman / Jenni Lu
FTI Consulting 
Direct: 203-722-8743 / 667-321-6018
... / ...
Media Contact:
Amy Phillips
Green Room Communications
Direct: 412-327-9499
...

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