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Astellas Pharma announces FDA approval of Izervay for GA

Astellas Pharma (ALPMY) announced the U.S. Food and Drug Administration approved Izervay for the treatment of geographic atrophy, or GA, secondary to age-related macular degeneration, or AMD, on August 4. “Izervay, a new complement C5 inhibitor, is the only approved GA treatment with a statistically significant reduction in the rate of GA progression at the 12-month primary endpoint across two Phase 3 clinical trials,” the company stated. Izervay, formerly Zimura/ACP, from Astellas will be a competitor in GA to Apellis’ (APLS) Syfovre.

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