US retinal disease specialist Apellis Pharmaceuticals (Nasdaq: APLS) has announced post hoc analyses from the 24-month, Phase III OAKS and DERBY studies evaluating Syfovre (pegcetacoplan injection) for the treatment of geographic atrophy (GA) secondary to age-related macular degeneration (AMD).
Syfovre was approved by the US Food and Drug Administration for this indication in February this year. Marketed as Empaveli, the systemic pegcetacoplan was previously approved by the FDA in 2021 for adults with paroxysmal nocturnal hemoglobinuria (PNH), a rare, life-threatening blood disease.
The latest analyses were reported during oral presentations at the Association for Research in Vision and Ophthalmology (ARVO) Annual Meeting taking place April 23-27 in New Orleans, USA.
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