Biogen's Subcutaneous LEQEMBI Application Accepted for Review in China

Reuters01-06

Biogen Inc. announced that its Biologics License Application for the subcutaneous formulation of LEQEMBI® (lecanemab) for the treatment of early Alzheimer's disease has been accepted for review in China. This regulatory review marks a significant step forward for Biogen and its collaboration arrangements with Eisai, as they seek to expand access to LEQEMBI for patients in new markets.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Biogen Inc. published the original content used to generate this news brief on January 05, 2026, and is solely responsible for the information contained therein.

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