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EyePoint Pharmaceuticals to Host Virtual Key Opinion Leader (KOL) Event on November 9, 2023

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EyePoint Pharmaceuticals, Inc. will host a virtual key opinion leader (KOL) event on November 9, 2023, to discuss EYP-1901 in wet age-related macular degeneration (wet AMD) and topline data considerations for the DAVIO 2 clinical trial. The event will feature presentations from retinal experts and will be moderated by EyePoint's CEO, Jay S. Duker, M.D.
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- KOLs to provide insight and discussion of EYP-1901 in wet AMD and topline data considerations for the DAVIO 2 clinical trial

WATERTOWN, Mass., Oct. 31, 2023 (GLOBE NEWSWIRE) -- EyePoint Pharmaceuticals, Inc. (NASDAQ: EYPT), a company committed to developing and commercializing therapeutics to improve the lives of patients with retinal diseases, today announced it will host a virtual key opinion leader (KOL) event on Thursday, November 9, 2023 from 8:00 to 9:00 am ET.

This event will focus on the potential of EYP-1901 in wet age-related macular degeneration (wet AMD), including KOL perspectives on the current wet AMD treatment landscape, vorolanib’s unique mechanism of action and outcome considerations for the upcoming topline data read-out for the DAVIO 2 trial in December. The event will be moderated by EyePoint’s President and Chief Executive Officer, Jay S. Duker, M.D., and will feature presentations from the following retinal experts:

  • David S. Boyer, M.D., Senior Partner at Retina-Vitreous Associates Medical Group, Adjunct Clinical Professor of Ophthalmology at University of Southern California, Keck School of Medicine
  • David R. Lally, M.D., Retinal Surgeon at Baystate Medical Center, Assistant Professor of Ophthalmology at the University of Massachusetts Medical School-Baystate, Director of Retina Research Institute at New England Retinal Consultants

To access the live conference call, please register using the audio conference link: https://register.vevent.com/register/BI7011e8a8a96a408b91e23c1c3f598ede. A live audio webcast of the event can be accessed via the Investors section of the Company website at www.eyepointpharma.com. A webcast replay will also be available on the corporate website at the conclusion of the call.

About EYP-1901

EYP-1901 is being developed as an investigational sustained delivery treatment for retinal disease combining a bioerodible formulation of EyePoint's proprietary Durasert® delivery technology (Durasert E™) with vorolanib, a tyrosine kinase inhibitor. Results from the Phase 1 DAVIO clinical trial of EYP-1901 in wet AMD showed a positive safety profile with stable visual acuity and OCT. Further, the data demonstrated an impressive treatment burden reduction of 75% at six months and 73% at the 12-month visit following a single dose of EYP-1901. Phase 2 trials are fully enrolled in wet AMD and non-proliferative diabetic retinopathy, and a diabetic macular edema trial is planned for initiation in Q1 2024. Vorolanib is licensed to EyePoint exclusively by Equinox Sciences for the localized treatment of all ophthalmic diseases.

About EyePoint Pharmaceuticals

EyePoint Pharmaceuticals (Nasdaq: EYPT) is a company committed to developing and commercializing therapeutics to help improve the lives of patients with retinal diseases. The Company's pipeline leverages its proprietary bioerodible Durasert E technology for sustained intraocular drug delivery including EYP-1901, an investigational sustained delivery intravitreal anti-VEGF treatment currently in Phase 2 clinical trials. The proven Durasert® drug delivery platform has been safely administered to over 80,000 patient eyes across four U.S. FDA approved products. EyePoint Pharmaceuticals is headquartered in Watertown, Massachusetts. For more information visit www.eyepointpharma.com.

Investors:
Christina Tartaglia
Stern IR
Direct: 212-698-8700
christina.tartaglia@sternir.com

Media Contact:
Amy Phillips
Green Room Communications
Direct: 412-327-9499
aphillips@greenroompr.com


EyePoint Pharmaceuticals will host the virtual KOL event on Thursday, November 9, 2023.

The KOL event will focus on the potential of EYP-1901 in wet AMD, including KOL perspectives on the current wet AMD treatment landscape and outcome considerations for the upcoming topline data read-out for the DAVIO 2 trial in December.

The KOL event will be moderated by EyePoint's President and CEO, Jay S. Duker, M.D.

The event will feature presentations from David S. Boyer, M.D., Senior Partner at Retina-Vitreous Associates Medical Group and Adjunct Clinical Professor of Ophthalmology at University of Southern California, Keck School of Medicine, and David R. Lally, M.D., Retinal Surgeon at Baystate Medical Center and Assistant Professor of Ophthalmology at the University of Massachusetts Medical School-Baystate, Director of Retina Research Institute at New England Retinal Consultants.

To access the live conference call, please register using the audio conference link: [link].

The live audio webcast of the event can be accessed via the Investors section of the EyePoint Pharmaceuticals' website at [website].

Yes, a webcast replay will be available on the EyePoint Pharmaceuticals' corporate website at the conclusion of the call.
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About EYPT

psivida corp., (nasdaq: psdv) (asx: pva) headquartered in watertown, ma, develops tiny, sustained release, drug delivery products designed to deliver drugs at a controlled and steady rate for months or years. psivida is currently focused on treatment of chronic diseases of the back of the eye utilizing its core technology systems, durasert™ and biosilicon™. the injectable, sustained release micro-insert iluvien® for the treatment of chronic diabetic macula edema (dme), licensed to alimera sciences, inc., has received marketing authorization in austria, france, germany, portugal, the u.k. spain, and italy. iluvien for dme has recently been approved in the us. psivida plans to institute pivotal phase iii clinical trials for the treatment of posterior uveitis with the same micro-insert as iluvien for dme. an investigator-sponsored clinical trial is ongoing for an injectable, bioerodible micro-insert to treat glaucoma and ocular hypertension. psivida's two fda-approved products, retisert®