Eisai Co., Ltd. is taking the early lead on the US commercial effort for Leqembi (lecanemab) in Alzheimer’s disease, but the company’s partner,Biogen, Inc., will add reinforcement – as long as the drug has approval for reimbursement from the Centers for Medicare and Medicaid Services (CMS) following full approval by the US Food and Drug Administration.
“The starting gate is really CMS approval,” Biogen CEO Christopher Viehbacher said during the company’s first quarter sales and earnings call on 25 April. “You want to flex your commercial...
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Scrip for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?