WATERTOWN, Mass., Aug. 02, 2021 (GLOBE NEWSWIRE) — EyePoint Pharmaceuticals, Inc. (NASDAQ: EYPT), a pharmaceutical company committed to developing and commercializing therapeutics to help improve the lives of patients with serious eye disorders, today announced the formation of its Executive Scientific Advisory Board (SAB), chaired by Dr. Carl Regillo M.D., FACS, Chief of the Retina Service at Wills Eye Hospital. Other members of the SAB include Drs. Sophie J. Bakri, M.D., Mayo Clinic, Caroline R. Baumal, M.D., Tufts Medical Center, David S. Boyer, M.D., University of Southern California Keck School of Medicine, Glenn J. Jaffe, M.D., Duke University, Rishi P. Singh, M.D., Cleveland Clinic, and Charles C. Wykoff, M.D., Ph.D., Retina Consultants of Texas. These prominent retinal surgeons and leaders in the field of vision will work with EyePoint management to advance a pipeline of ocular products that advance the treatment paradigm for better patient outcomes.

“We are very honored to have such distinguished and talented experts sit on EyePoint Pharmaceuticals’ executive scientific advisory board,” said Nancy Lurker, Chief Executive Officer of EyePoint Pharmaceuticals “and it is a testament to the quality of our science and pipeline potential that they are now advising us. Their combined knowledge, insight, experience, and strategic council will prove vital as we approach interim 6-month data for our Phase 1 DAVIO trial of EYP-1901 for the potential treatment of wet-AMD and continue to advance our innovative pipeline of treatments for patients with serious ophthalmic diseases.”

Carl D. Regillo, M.D., FACS – Chairman of the Executive Scientific Advisory Board



Dr. Carl D. Regillo is a globally recognized leader in the retinal surgery field, a Professor of Ophthalmology at Thomas Jefferson University, Chief of the Retina Service of Wills Eye Hospital and Founder of the Wills Eye Clinical Retina Research Unit in Philadelphia. He has been an investigator on numerous major clinical trials developing new medical and surgical treatments for retinal disorders such as macular degeneration and diabetic retinopathy. Dr. Regillo has authored over 200 publications along with over 50 book chapters and 9 major books. He is invited to lecture worldwide and serves on the scientific editorial board for several top ophthalmology peer-reviewed journals, and is a recipient of numerous local, national, and international awards including American Academy of Ophthalmology Achievement, Senior Achievement, Secretariat, and Lifetime Achievement Awards and the American Society of Retinal Specialists Honor, Senior Honor and Founders Awards. He is also a charter inductee of the Retina Hall of Fame and named in the Ophthalmologist Power List of the top 100 most influential ophthalmologists in the world. He received his medical degree from Harvard Medical School and performed his ophthalmology residency and vitreoretinal fellowship at Wills Eye Hospital.

Sophie J. Bakri, M.D., M.B.A.



Sophie J. Bakri, M.D., M.B.A. is Chair of the Department of Ophthalmology at Mayo Clinic, Rochester, MN and holds the Whitney and Betty MacMillan Professorship in Ophthalmology in Honor of Robert R. Waller, M.D. She has authored over 200 peer-reviewed papers and 26 book chapters. She is a principal investigator on numerous multicenter clinical trials on novel drugs for retinal disease. She serves on the Editorial Board of the American Journal of Ophthalmology, Retina, Seminars in Ophthalmology and OSLI Retina. She has served on committees at the Macula Society, Retina Society and AAO, and is a Board Member of the American Society of Retinal Specialists.

Caroline R. Baumal, M.D., FASRS



Caroline R. Baumal, M.D., FASRS is a Professor of Ophthalmology at New England Eye Center, Tufts Medical Center in Boston, MA. She specializes in medical and surgical disorders of the retina and vitreous. Her research interests include novel retinal imaging and drug development. She has been appointed to the ASRS Retina Hall of Fame and was on the Top 100 Female Ophthalmology list from 2021. Dr. Baumal has authored over 165 publications, 28 book chapters on retinal diseases and recently edited the book Treatment of Diabetic Retinopathy.

Glenn J. Jaffe, M.D.



Dr. Jaffe is the Robert Machemer Professor of Ophthalmology and a member of the vitreoretinal faculty at Duke University Eye Center. He is chief of the Retina Division, and founded and directs the Duke Reading Center. Dr. Jaffe received his medical degree and his ophthalmology residency training at the University of California, San Francisco. He completed a two-year combined clinical and research vitreoretinal fellowship at the Medical College of Wisconsin. He joined the faculty at Duke University in 1989. Dr. Jaffe serves on the Editorial Board of the journals Retina, Current Opinions in Ophthalmology, and Ocular Surgery News and reviews manuscripts for a variety of clinical and investigative ophthalmology journals.

Rishi P. Singh, M.D.



Dr. Rishi P. Singh, M.D. is a staff surgeon at the Cole Eye Institute, Cleveland Clinic and Professor of Ophthalmology at the Lerner College of Medicine in Cleveland Ohio. He also currently serves as the medical director of informatics at the Cleveland Clinic. He specializes in the treatment of medical and surgical retinal disease such as diabetic retinopathy, retinal detachment, and age-related macular degeneration. Dr. Singh has authored more than 190 peer reviewed publications, books, and book chapters and serves as the principal investigator of numerous national clinical trials advancing the treatment of retinal disease. Dr. Singh is the former president on the Retina World Congress and is a board member of the American Society of Retina Specialists.

David S. Boyer, M.D.



David S. Boyer, M.D. is a Board-certified ophthalmologist specializing in the treatment of diseases of the retina and vitreous. He is Senior Partner at Retina-Vitreous Associates Medical Group with offices in Los Angeles, Beverly Hills, North Hollywood, Torrance, Pasadena, Tarzana and Glendale, California. Dr. Boyer is an Adjunct Clinical Professor of Ophthalmology with the University of Southern California/Keck School of Medicine in Los Angeles, CA. He is one of the leading retinal clinical researchers in the country for new treatments in macular degeneration and diabetic macular edema.

Charles C. Wykoff, M.D., Ph.D.



Charles C. Wykoff, M.D., Ph.D. is Director of the Retina Consultants of Texas Research Centers; Chairman of the Research and Clinical Trials Committee, Retina Consultants of America; and Deputy Chair of Ophthalmology for the Blanton Eye Institute, Houston Methodist Hospital. Dr. Wykoff serves as principal investigator for numerous clinical trials. He has published nearly 200 peer-reviewed manuscripts and frequently speaks at national and international academic meetings. Dr. Wykoff serves on multiple scientific and medical advisory boards, safety monitoring committees, and global steering committees for endeavors spanning the innovative process from early to late stage developments. He is President of the Vit-Buckle Society and serves on the ASRS Board of Directors as Chair of the Practice Management Committee. He has been awarded the ASRS Senior Honor and Young Investigator Awards as well as the AAO Secretariat and multiple Achievement Awards.

Additional background information on the SAB members can be found on our website,


www.eyepointpharma.com

About EyePoint Pharmaceuticals, Inc.

(Nasdaq:EYPT) is a pharmaceutical company committed to developing and commercializing therapeutics to help improve the lives of patients with serious eye disorders. The Company’s pipeline leverages its proprietary Durasert

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technology for sustained intraocular drug delivery including EYP-1901, a potential twice-yearly intravitreal anti-VEGF treatment initially targeting wet age-related macular degeneration. The Company has two commercial products: YUTIQ

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, for the treatment of chronic non-infectious uveitis affecting the posterior segment of the eye, and DEXYCU

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, for the treatment of postoperative inflammation following ocular surgery. EyePoint Pharmaceuticals is headquartered in Watertown, Massachusetts. To learn more about the Company, please visit

www.eyepointpharma.com

and connect on Twitter and LinkedIn.

SAFE HARBOR STATEMENTS UNDER THE PRIVATE SECURITIES LITIGATION ACT OF 1995: To the extent any statements made in this press release deal with information that is not historical, these are forward-looking statements under the Private Securities Litigation Reform Act of 1995. Such statements include, but are not limited to, statements regarding the anticipated use of proceeds for the proposed offering and other statements identified by words such as “will,” “potential,” “could,” “can,” “believe,” “intends,” “continue,” “plans,” “expects,” “anticipates,” “estimates,” “may,” other words of similar meaning or the use of future dates. Forward-looking statements by their nature address matters that are, to different degrees, uncertain. Uncertainties and risks may cause EyePoint’s actual results to be materially different than those expressed in or implied by EyePoint’s forward-looking statements. For EyePoint, this includes our expectations regarding the timing and clinical development of our product candidates, including EYP-1901; the potential for EYP-1901 as a novel twice-yearly treatment for serious eye diseases, including wet age-related macular degeneration, diabetic retinopathy and retinal vein occlusion; the effectiveness and timeliness of clinical trials, and the usefulness of the data; the timeliness of regulatory approvals; the continued impact of the COVID-19 pandemic on EyePoint’s business, the medical community and the global economy and the impact of general business and economic conditions; our ability to achieve profitable operations and access to needed capital; fluctuations in our operating results; our ability to successfully produce sufficient commercial quantities of YUTIQ and DEXYCU and to successfully commercialize YUTIQ and DEXYCU in the U.S.; our ability to sustain and enhance an effective commercial infrastructure and enter into and maintain commercial agreements for YUTIQ and DEXYCU; the development of our YUTIQ line extension shorter-duration treatment for non-infectious uveitis affecting the posterior segment of the eye; the success of current and future license agreements, including our agreements with Ocumension Therapeutics and Equinox Science; termination or breach of current license agreements, including our agreements with Ocumension Therapeutics and Equinox Science; our dependence on contract research organizations, co-promotion partners, and other outside vendors and service providers; effects of competition and other developments affecting sales of products; market acceptance of products; effects of guidelines, recommendations and studies; protection of intellectual property and avoiding intellectual property infringement; retention of key personnel; product liability; industry consolidation; compliance with environmental laws; manufacturing risks; risks and costs of international business operations; volatility of stock price; possible dilution; absence of dividends; and other factors described in our filings with the Securities and Exchange Commission. We cannot guarantee that the results and other expectations expressed, anticipated or implied in any forward-looking statement will be realized. A variety of factors, including these risks, could cause our actual results and other expectations to differ materially from the anticipated results or other expectations expressed, anticipated or implied in our forward-looking statements. Should known or unknown risks materialize, or should underlying assumptions prove inaccurate, actual results could differ materially from past results and those anticipated, estimated or projected in the forward-looking statements. You should bear this in mind as you consider any forward-looking statements. Our forward-looking statements speak only as of the dates on which they are made. We do not undertake any obligation to publicly update or revise our forward-looking statements even if experience or future changes makes it clear that any projected results expressed or implied in such statements will not be realized.

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