Eisai/Pfizer's acetylcholinesterase inhibitor Aricept (donepezil) waslicensed in the UK earlier this year for the symptomatic treatment of mild-to-moderately severe Alzheimer's dementia (Marketletter March 3). However, its efficacy and safety has been questioned in a report published in the Drugs and Therapeutics Bulletin (October issue).
The article says that as donepezil increases cholinergic transmission, then its therapeutic benefits "must depend on the presence of functioning cholinergic neurones." In that case, the therapeutic effects of an acetylcholinesterase inhibitor must diminish during the course of the disease as the number of cholinergic neurones decreases.
Data Not Fully Published The report goes on to say that only one trial, including 161 patients with mild-to-moderately-severe Alzheimer's disease, has been published in full; data from an open-label study looking at long-term treatment with donepezil has been published in abstract form only, as have the results from a Phase III, 450-patient trial.
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