AbbVie (NYSE: ABBV) has announced a $3.5 billion non-cash impairment charge related to its potential schizophrenia treatment, emraclidine, following the drug's failure in Phase II trials last year.
Studies of emraclidine, which was acquired in the $8.7 billion purchase of Cerevel Therapeutics, failed to meet primary goals, prompting a reassessment of the program in November.
Researchers have expressed high hopes for the drug, a selective M4 muscarinic modulator, as a potentially novel offering in schizophrenia. Designed as a once-daily oral therapy for managing acute psychotic symptoms, it was the key driver of AbbVie’s Cerevel acquisition.
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