BRIEF-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

Reuters

01/26

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

Source text: ID:nPn22MRca

Further company coverage: [4523.T BIIB.O]

((Reuters.Briefs@thomsonreuters.com;))

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