EyePoint Pharmaceuticals Announces Presentations at Eyecelerator 2023, American Academy of Ophthalmology Annual Meeting 2023 and Guggenheim’s 5th Annual Inflammation, Neurology & Immunology Conference 2023
EyePoint Pharmaceuticals, Inc. will present at upcoming medical meetings and an investor conference. Dr. Duker will present interim safety data for EYP-1901 with no reported serious adverse events. Dr. Avery will present preclinical data showing the neuroprotective effect of vorolanib. The presentations can be accessed on the company's website.
Positive
The safety data for EYP-1901 shows an excellent safety profile with no reported serious adverse events.
Preclinical data demonstrates that vorolanib has a neuroprotective effect against photoreceptor degeneration.
Investors can access the presentations on EyePoint Pharmaceuticals' website.
10/30/2023 - 07:00 AM
WATERTOWN, Mass., Oct. 30, 2023 (GLOBE NEWSWIRE) -- EyePoint Pharmaceuticals, Inc. (NASDAQ: EYPT), a pharmaceutical company committed to developing and commercializing therapeutics to improve the lives of patients with retinal diseases, today announced that the Company will present at upcoming medical meetings and an investor conference.
Presentation details are as follows:
Eyecelerator 2023
Title: The Year in Review
Dr. Duker will present interim masked safety data through October 1, 2023, in which approximately 173 patients have received EYP-1901 with a minimum of four months of follow-up post injection from the ongoing Phase 2 PAVIA and DAVIO 2 clinical trials and the completed DAVIO 1 trial. The results demonstrate the excellent safety profile of EYP-1901 with no reported drug-related ocular serious adverse events (SAEs) or drug-related systemic SAEs.
American Academy of Ophthalmology (AAO) Annual Meeting 2023
Title: Receptor Inhibition and Neuroprotection with Tyrosine Kinase Inhibitor Vorolanib for Retinal and Choroidal Diseases
Dr. Avery will present preclinical data from a validated rodent retinal detachment model, which demonstrated that vorolanib, the active drug in EYP-1901, significantly reduced the severity of change in baseline visual acuity and improved contrast thresholds in mice treated with vorolanib compared with placebo, suggesting a neuroprotective effect against photoreceptor degeneration.
Guggenheim’s 5th Annual Inflammation, Neurology & Immunology Conference 2023
Forum: Fireside Chat
The Eyecelerator and AAO Annual Meeting presentation materials and a webcast and subsequent archived replay of the Guggenheim fireside chat may be accessed via the Investors section of the Company website at www.eyepointpharma.com .
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 thousands of patients' 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@sternir.com
Media Contact aphillips@greenroompr.com
The safety data showed an excellent safety profile with no reported serious adverse events.
The preclinical data demonstrated that vorolanib has a neuroprotective effect against photoreceptor degeneration.
Investors can access the presentations on EyePoint Pharmaceuticals' website.
EyePoint Pharmaceuticals Inc
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Analytical Laboratory Instrument Manufacturing
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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®
