After the debacle surrounding Aduhelm (aducanumab), Leqembi (lecanemab) was supposed to be the Alzheimer’s amyloid beta-directed antibody that delivered results for patients and its manufacturers Eisai (TYO: 4523) and Biogen (Nasdaq: BIIB).
But, as of January 26, just 2,000 American patients were receiving the drug, a trajectory that is well behind the 10,000 by the end of March target that Eisai previously set.
Analysts have questioned to what extent neurologists believe Leqembi represents an improvement over older Alzheimer’s treatments, which are largely powerless at slowing the course of the devastating disease themselves.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze