Welcome to our dedicated page for EyePoint news (Ticker: EYPT), a resource for investors and traders seeking the latest updates and insights on EyePoint stock.
EyePoint, Inc. develops and commercializes therapeutics for serious retinal diseases as a clinical-stage biopharmaceutical company. Its lead product candidate, DURAVYU (vorolanib intravitreal insert), is an investigational sustained-delivery treatment that uses bioerodible Durasert E technology and is being studied for wet age-related macular degeneration and diabetic macular edema.
Recurring EyePoint news covers clinical program updates, financial results, FDA naming and product-status disclosures, manufacturing and commercial-readiness topics, investor presentations, and equity inducement grants under Nasdaq Listing Rule 5635(c)(4). Company updates also address cash resources, corporate development activity, and disclosures tied to its Nasdaq-listed common stock.
EyePoint Pharmaceuticals (NASDAQ: EYPT) announced encouraging six-month interim data from its Phase 1 DAVIO clinical trial of EYP-1901, an anti-VEGF treatment for wet age-related macular degeneration (AMD). Presented at the AAO 2021 Meeting, the trial involved 17 patients, showcasing a 79% reduction in treatment burden and no serious adverse events reported. Patients experienced sustained visual acuity with 76% and 53% not needing rescue therapy after four and six months, respectively. EyePoint plans to advance EYP-1901 into Phase 2 trials in 2022 and engage with the FDA regarding registration trials.
EyePoint Pharmaceuticals, Inc. (NASDAQ: EYPT) will have CEO Nancy Lurker present at two virtual conferences: the Jefferies London Healthcare Conference on November 18, 2021, at 3:00 a.m. ET and the 33rd Annual Piper Sandler Virtual Healthcare Conference on November 22, 2021, at 10:00 a.m. ET. The company focuses on developing therapeutics for serious eye disorders, including its Durasert® technology. Webcasts of the presentations will be available on their website, with replays accessible for 30 and 90 days, respectively.
EyePoint Pharmaceuticals (NASDAQ: EYPT) will host a conference call on November 13 at 12:00 P.M. ET to discuss interim data from its Phase 1 DAVIO trial of EYP-1901, aimed at treating wet AMD. The interim results will be presented by Dr. David Boyer during the AAO Retina Subspecialty Day. EYP-1901 is designed for sustained drug delivery through the company's proprietary Durasert technology, which may provide a twice-yearly treatment option for patients. The event will be accessible via phone and webcast on the company's website.
EyePoint Pharmaceuticals (NASDAQ: EYPT) reported its Q3 2021 financial results, highlighting a 49% increase in net product revenue, totaling $8.6 million compared to $5.8 million in the same quarter last year. The Company presented positive safety data from the Phase 1 DAVIO trial for EYP-1901 targeting wet AMD at the ASRS 2021 Annual Meeting. Operating expenses rose to $24.4 million, leading to a net loss of $16.7 million or ($0.58) per share. However, cash reserves improved to $119.7 million, supporting operations through 2022.
EyePoint Pharmaceuticals (NASDAQ: EYPT) has appointed Dr. Jay S. Duker as Chief Operating Officer, expanding his role from Chief Strategic Scientific Officer. Dr. Duker, who has been part of the EyePoint team since 2020, has extensive experience in retinal disease and entrepreneurship. His leadership aims to enhance EyePoint's development of next-generation ophthalmic therapeutics, including the promising EYP-1901 for wet AMD. The company is excited about his ability to lead clinical and product development as it strives to address significant eye disorders.
EyePoint Pharmaceuticals, Inc. (NASDAQ: EYPT) will host a conference call on November 3, 2021, at 8:30 a.m. ET to discuss its Q3 2021 financial results and recent business developments. This call is part of the company's commitment to improving therapeutics for serious eye disorders, utilizing its proprietary Durasert® technology. EyePoint's pipeline includes EYP-1901, targeting wet age-related macular degeneration, alongside its commercial products, YUTIQ® and DEXYCU®.
EyePoint Pharmaceuticals (NASDAQ: EYPT) announced positive interim safety data from its Phase 1 DAVIO clinical trial of EYP-1901 for wet age-related macular degeneration. The trial shows no serious ocular or systemic adverse events after 3 months, indicating a robust safety profile. Additionally, the ongoing YUTIQ® CALM registry study continues to gather real-world data on patients treated with fluocinolone acetonide intravitreal implant. EYP-1901 aims to offer a twice-yearly treatment solution for patients suffering from this retinal disease.
EyePoint Pharmaceuticals (NASDAQ: EYPT) announced the selection of a late-breaking abstract for the Phase 1 DAVIO trial of EYP-1901 in wet age-related macular degeneration (AMD) for presentation at the American Academy of Ophthalmology 2021 Annual Meeting, scheduled for November 12-15, 2021.
The presentation will feature topline data and is set for November 13, 2021, at 9:07 AM CST, presented by David S. Boyer MD. EYP-1901 aims to provide sustained delivery treatment via a single injection, with key endpoints including safety and visual acuity.
EyePoint Pharmaceuticals, Inc. (NASDAQ: EYPT) announced its senior management will present at four upcoming conferences. The presentations include:
- Ophthalmology Futures Euro Forums 2021 on September 8, 2021, featuring Jay Duker, M.D.
- H.C. Wainwright 23rd Annual Global Investor Conference on September 13, 2021.
- Cantor Fitzgerald Virtual Global Healthcare Conference on September 29, 2021.
- Benzinga Healthcare Small Cap Conference on September 30, 2021.
Recordings and webcasts will be available on their website.
EyePoint Pharmaceuticals (NASDAQ: EYPT) announced that CEO Nancy Lurker will present at the H.C. Wainwright Ophthalmology Virtual Conference on August 17, 2021. The presentation will be accessible for on-demand viewing starting at 9:00 a.m. ET on the company’s website, with a replay available for 90 days. EyePoint focuses on innovative therapeutics for serious eye disorders, leveraging its Durasert® technology. The company’s current portfolio includes YUTIQ® and DEXYCU®, targeting chronic non-infectious uveitis and postoperative inflammation, respectively.