EyePoint to Present at the 43rd Annual J.P. Morgan Healthcare Conference
17 Diciembre 2024 - 6:00AM
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 43rd Annual
J.P. Morgan Healthcare Conference in San Francisco on Tuesday,
January 14, 2025 at 2:15 p.m. PT/5:15 p.m. ET.
A webcast and subsequent archived replay of the presentation may
be accessed via the Investors section of the Company website at
www.eyepointpharma.com.
About EyePoint Pharmaceuticals
EyePoint (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™ (f/k/a 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 3 global, pivotal 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 in a Phase 2 clinical trial in
diabetic macular edema (DME). EyePoint expects full topline data
from the Phase 2 clinical trial in DME in Q1 2025 and topline data
from both Phase 3 pivotal trials in wet AMD in 2026.
Pipeline programs include EYP-2301, a 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 Direct:
212-698-8700christina.tartaglia@sternir.com
Media Contact:
Amy PhillipsGreen Room CommunicationsDirect:
412-327-9499aphillips@greenroompr.com
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