Apellis Reports SYFOVRE Delays Geographic Atrophy Progression by 1.5 Years in Five-Year Study

Reuters11-12

Apellis Reports SYFOVRE Delays Geographic Atrophy Progression by 1.5 Years in Five-Year Study

Apellis Pharmaceuticals Inc. has announced data from a post hoc analysis of the GALE extension study, evaluating the long-term effects of SYFOVRE® (pegcetacoplan injection) in patients with geographic atrophy (GA) secondary to age-related macular degeneration. The study showed that five years of continuous treatment with SYFOVRE delayed GA lesion growth by approximately 1.5 years in patients with nonsubfoveal GA compared to sham/projected sham. The safety profile remained consistent with previous data. The company stated that detailed results will be presented at a future medical meeting.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Apellis Pharmaceuticals Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9573528-en) on November 12, 2025, and is solely responsible for the information contained therein.

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The study showed that five years of continuous treatment with SYFOVRE delayed GA lesion growth by approximately 1.5 years in patients with nonsubfoveal GA compared to sham/projected sham. The safety profile remained consistent with previous data. The company stated that detailed results will be presented at a future medical meeting.\n      \n\nDisclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Apellis Pharmaceuticals Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. 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