Chinese regulators have granted priority review to a biologics license application for a subcutaneous autoinjector formulation of Leqembi (lecanemab) for early Alzheimer’s disease, Eisai said on February 9.The application, which was accepted by China’s National Medical Products Administration in January,…
To read the full story
Related Article
- Leqembi Subcutaneous Autoinjector Approved in China
September 4, 2026
- China Accepts BLA for Leqembi Subcutaneous Autoinjector: Eisai
January 7, 2026
BUSINESS
- Roche Proposes Ex-Takeda CEO Weber for Board
September 24, 2026
- Moderna Launches XFG-Updated mNEXSPIKE in Japan
September 24, 2026
- FDA Accepts Tanabe’s EPP/XLP Drug for Priority Review
September 24, 2026
- GenAI Use at Japan Pharmas Rises to 92% in 2026: Funlead Survey
September 24, 2026
- Japan OKs FoundationOne CDx for Pfizer’s Lorbrena
September 24, 2026
We had just gotten off a call with a client in Europe, and we’d received a bit of an earful. “Philip,” the client pressed, “what can this candidate bring to us? We know what he does, but what has he…





