Eisai & Biogen Say U.S. FDA Accepts Leqembi Supplemental Biologics License Application As Subcutaneous Starting Dose For Treatment Of Early Alzheimer's Under Priority Review
ReutersJan 25, 2026 11:36 PM
Jan 25 (Reuters) - Eisai Co Ltd 4523.T:
FDA ACCEPTS LEQEMBI® IQLIKTM (LECANEMAB-IRMB) SUPPLEMENTAL BIOLOGICS LICENSE APPLICATION AS A SUBCUTANEOUS STARTING DOSE FOR THE TREATMENT OF EARLY ALZHEIMER'S DISEASE UNDER PRIORITY REVIEW
Further company coverage: [4523.T BIIB.O]
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