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FDA accepts Eisai’s BLA for LEQEMBI subcutaneous autoinjector for alzheimer’s disease treatment

Express Pharma

The FDA has set a Prescription Drug User Fee Act (PDUFA) action date for August 31, 2025. This may reduce the need for hospital visits and nursing care for IV administration, potentially making long-term maintenance easier for patients. LEQEMBI is already approved in several regions, including the U.S.,