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EyePoint to Present at Guggenheim SMID Cap Biotech Conference

Key Takeaway: EyePoint Pharmaceuticals, Inc. has announced its participation in the Guggenheim SMID Cap Biotech Conference, where CEO Jay S. Duker will engage in a fireside chat. The company is currently advancing its lead product candidate, DURAVYU, through Phase 3 clinical trials for wet age-related macular degeneration, with topline data expected in 2026. Additionally, EyePoint's pipeline includes other investigational therapies utilizing its proprietary Durasert technology. The company focuses on innovative treatments for serious retinal diseases.
Price reaction · baseline $7.73 (2025-01-29 close) · hit after-hours · clean, no other EYPT news in the window
day 0 close · peak
+4.1%

Market Sentiment Analysis

POSITIVE FACTORS

  • EyePoint Pharmaceuticals will participate in an important biotech conference, highlighting its visibility in the industry.
  • The company's lead candidate, DURAVYU, is in advanced Phase 3 trials, indicating strong progress in drug development.
  • EyePoint's proprietary Durasert technology has been successfully administered in several FDA-approved products.

CONCERNS & RISKS

  • The timeline for FDA approval of DURAVYU is uncertain, introducing a risk of delayed market entry.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+28%
120-day peak, hindsight
Typical move
53.1%
average across 5 past catalysts
Cash runway
~8 mo
Medium dilution risk
Lead asset
EYP-1901
Phase 3 · Wet Age Related Macular Degeneration

Full Press Release Details

WATERTOWN, Mass., Jan. 30, 2025 (GLOBE NEWSWIRE) -- 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 will participate in a fireside chat at the Guggenheim SMID Cap Biotech Conference on Thursday, February 6, 2025 at 9:30 a.m. ET.
A webcast and subsequent archived replay of the fireside chat 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.

Frequently Asked Questions

When is EyePoint Pharmaceuticals' fireside chat scheduled?

The fireside chat is on February 6, 2025, at 9:30 a.m. ET.

What is EyePoint Pharmaceuticals' main focus?

EyePoint focuses on developing therapeutics for serious retinal diseases.

What is DURAVYU™ used for?

DURAVYU™ is an investigational treatment for VEGF-mediated retinal diseases.

When will EyePoint report Phase 2 DME data?

Topline data from the Phase 2 DME trial is expected in Q1 2025.

Where can I access the fireside chat webcast?

The webcast will be available in the Investors section of EyePoint's website.

Last updated: Jan 30, 2025