EyePoint Pharmaceuticals to Present at the H.C. Wainwright 4th Annual Ophthalmology Virtual Conference
08 August 2024 - 9:00PM
EyePoint Pharmaceuticals, Inc. (NASDAQ: EYPT), a company committed
to developing and commercializing innovative therapeutics to
improve the lives of patients with serious retinal diseases, today
announced that Jay S. Duker, M.D., President and Chief Executive
Officer of EyePoint Pharmaceuticals will present at the H.C.
Wainwright 4th Annual Ophthalmology Virtual Conference:
- Company
OverviewDate: Thursday, August 15th, 2024Time: Available
on-demand at 7:00 a.m. ET
- The Evolving Therapeutic
Landscape of AMD Panel DiscussionDate: Thursday, August
15th, 2024Time: 9:00 a.m. ET
A live webcast and subsequent archived replay of
the panel and the on-demand company overview may be accessed via
the Investors section of the Company website at
www.eyepointpharma.com. The replay will be available for 90 days
after the event.
About EyePoint
Pharmaceuticals
EyePoint Pharmaceuticals (Nasdaq: EYPT) is a
clinical-stage biopharmaceutical company committed to developing
and commercializing innovative therapeutics to help improve the
lives of patients with serious retinal diseases. The Company's
pipeline leverages its proprietary bioerodible Durasert E™
technology for sustained intraocular drug delivery. The Company’s
lead product candidate, DURAVYU™ (previously known as EYP-1901), is
an investigational sustained delivery treatment for VEGF-mediated
retinal diseases combining vorolanib, a selective and
patent-protected tyrosine kinase inhibitor with bioerodible
Durasert E™. DURAVYU is presently in Phase 2 clinical trials as a
sustained delivery treatment for wet age-related macular
degeneration (wet AMD), the leading cause of vision loss among
people 50 years of age and older in the United States, and diabetic
macular edema (DME). EyePoint expects to randomize patients for
inclusion in pivotal Phase 3 clinical trials in wet AMD in
2024.
Pipeline programs include EYP-2301, a promising
TIE-2 agonist, razuprotafib, formulated in Durasert E™ to
potentially improve outcomes in serious retinal diseases. The
proven Durasert® drug delivery technology has been safely
administered to thousands of patient eyes across four U.S. FDA
approved products. EyePoint Pharmaceuticals is headquartered in
Watertown, 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.
DURAVYU™ has been conditionally accepted by the
FDA as the proprietary name for EYP-1901. DURAVYU is an
investigational product; it has not been approved by the FDA. FDA
approval and the timeline for potential approval is uncertain.
Investors:
Christina TartagliaPrecision AQ (formerly Stern
IR)Direct: 212-698-8700christina.tartaglia@precisionaq.com
Media Contact:
Amy PhillipsGreen Room CommunicationsDirect:
412-327-9499aphillips@greenroompr.com
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