FDA approves Apellis' retinal disease drug as competitor expects August decision
The FDA approved Apellis Pharmaceuticals’ drug for geographic atrophy secondary to age-related macular degeneration after pushing back the green light decision by three months to go through more data.
The biotech will market the drug as Syfovre. Known investigationally as pegcetacoplan injection, Apellis already markets a version of the drug as Empaveli for the rare disease paroxysmal nocturnal hemoglobinuria.
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