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Biologics License Application for Subcutaneous Formulation of “LEQEMBI®” (lecanemab) for the Treatment of Early Alzheimer’s Disease Accepted in China

If approved, lecanemab may become the first and only anti-amyloid treatment in China to offer an at-home injection from the initiation of treatment for this progressive, relentless diseaseTOKYO and CAMBRIDGE, Mass., Jan. 05, 2026 (GLOBE NEWSWIRE) -- Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo Naito, “Eisai”) and Biogen Inc. (Nasdaq: BIIB, Corporate headquarters: Cambridge, Massachusetts, CEO: Christopher A. Viehbacher, “Biogen”) announced today that the Biologics License Application (BLA) f

articleEisai Co., Ltd.January 5, 202611/company/eisai-co-ltd/news/biologics-license-application-for-subcutaneous-formulation-of-leqembir-lecanemab-for-the-treatment-of-early-alzheimers-disease-accepted-in-china-1
Biologics License Application for Subcutaneous Formulation of “LEQEMBI®” (lecanemab) for the Treatment of Early Alzheimer’s Disease Accepted in China

About this update from Eisai Co., Ltd.

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More updates from Eisai Co., Ltd.

Biologics License ApplicationEisai Co., Ltd.ADChinaBiogen Inc.regulatory submissionsLEQEMBIregulatory approvalclinical study