Eisai/Biogen’s Lecanemab Faces Smoother Passage Through US FDA Than Aducanumb

With amyloid plaque reduction established as a surrogate endpoint by Aduhelm’s accelerated approval for Alzheimer’s disease, lecanemab is unlikely to face an advisory committee before its 6 January user fee goal date.

Smooth sailing
The regulatory sailing should be smoother for Eisai/Biogen's second-in-class amyloid-targeted antibody lecanemab. • Source: Shutterstock

More from Product Reviews

More from Pink Sheet