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See the DrugPatentWatch profile for Syfovre
Syfovre (pegcetacoplan) received FDA approval on February 15, 2024 for the treatment of adult patients with geographic atrophy (GA) secondary to age-related macular degeneration (AMD). [1]
Syfovre is marketed by Apellis Pharmaceuticals and is used for geographic atrophy (GA) due to AMD in adults. [1]
You can confirm the approval information and related coverage on DrugPatentWatch.com here: [1]
[1] https://www.drugpatentwatch.com/
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