New evidence published in the August 29 edition of the New England Journal of Medicine suggests that therapy with Boehringer Ingelheim's Micardis (telmisartan), initiated soon after an ischemic stroke and continued for two and a half years, does not significantly lower the rate of recurrent stroke, major cardiovascular events or diabetes.
Elevated blood pressure is the most serious risk factor for stroke, which is the most frequent cause of death in the world, responsible for about five millions deaths each year. This is the latest trial where improvment in a surrogate endpoint risk factor did not translate into clinical benefit.
UK drug major GlaxoSmithKline's blockbuster diabetes drug Avandia (rosiglitazone) has been under scrutiny since last year, when a meta-study published in the NEJM linked the drug with an increased risk of myocardial infarction (Marketletter May 28, 2007). Ongoing mixed news has seen GSK's sales of the drug drop to L1.22 billion ($2.43 billion) last year from L1.60 billion the year earlier.
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