February 7, 2022
NEW YORK–(BUSINESS WIRE)–Feb. 7, 2022– IVERIC Bio, Inc. (Nasdaq: ISEE) announced today that new post-hoc analyses from the GATHER1 Zimura® (avacincaptad pegol) Phase 3 clinical trial for the treatment of Geographic Atrophy (GA) secondary to Age-related Macular Degeneration will be presented at the upcoming Angiogenesis, Exudation, and Degeneration 2022 meeting taking place virtually on February 11 and 12, 2022.
“We are excited to have these new analyses of the GATHER1 clinical trial presented at the upcoming Angiogenesis meeting,” stated Pravin U. Dugel, MD, President of Iveric Bio. “While the analyses are considered exploratory we believe they further highlight the potential for Zimura to slow the progression of disease and preserve foveal anatomy in patients with GA secondary to AMD.”
The analyses will be presented in oral sessions. Details of the presentations are as follows:
Presentation Title: Evaluation of GA Growth Parameters and Impact on Foveal Progression: Post Hoc Analysis of the GATHER1 Trial
Presentation Title: Novel OCT Findings Regarding “Nascent GA at Risk” and Directionality of GA Progression in the GATHER1 Trial
Iveric Bio will issue a press release relating to the results of the post-hoc analyses and make the slides available on the Company’s website on the Events and Presentation page at the start of the presentations.
About Iveric Bio
Iveric Bio is a science-driven biopharmaceutical company focused on the discovery and development of novel treatments for retinal diseases with significant unmet medical needs. The Company is committed to having a positive impact on patients’ lives by delivering high-quality, safe and effective treatments designed to address debilitating retina diseases including all stages of age-related macular degeneration. For more information on the Company, please visit www.ivericbio.com.
Any statements in this press release or made during the presentation referenced herein about Iveric Bio’s future expectations, plans and prospects constitute forward-looking statements for purposes of the safe harbor provisions under the Private Securities Litigation Reform Act of 1995. Forward-looking statements include any statements about the Company’s strategy, future operations and future expectations and plans and prospects for the Company, and any other statements containing the words “anticipate,” “believe,” “estimate,” “expect,” “intend”, “goal,” “may”, “might,” “plan,” “predict,” “project,” “seek,” “target,” “potential,” “will,” “would,” “could,” “should,” “continue,” and similar expressions. In this press release, the Company’s forward looking statements include statements about its expectations regarding its development and regulatory strategy for Zimura, its plans for additional indications, such as intermediate AMD, that the Company may pursue for the development of Zimura, the potential utility of Zimura and the clinical meaningfulness of clinical trial results. Such forward-looking statements involve substantial risks and uncertainties that could cause the Company’s development programs, future results, performance, or achievements to differ significantly from those expressed or implied by the forward-looking statements. Such risks and uncertainties include, among others, those related to the progress and success of research and development programs and clinical trials, and other factors discussed in the “Risk Factors” section contained in the quarterly and annual reports that the Company files with the Securities and Exchange Commission. Any forward-looking statements represent the Company’s views only as of the date of this press release. The Company anticipates that subsequent events and developments may cause its views to change. While the Company may elect to update these forward-looking statements at some point in the future, the Company specifically disclaims any obligation to do so except as required by law.
Kathy Galante, 212-845-8231
Senior Vice President, Investor Relations
Alex Van Rees, 973-442-1555 ext. 111
Source: IVERIC Bio, Inc.