Israeli pharmaceutical major Teva says that relapsing-remitting multiple sclerosis patients failing Avonex (interferon beta-1a) therapy achieved significant reductions in relapse rates and in Expanded Disability Status Scale scores after switching to its drug Copaxone (glatiramer acetate injection).
In a study published in the June issue of the European Journal of Neurology, Teva's selective selective MHC class II modulator reduced annual relapse rate an additional 57% over US drugmaker Biogen Idec's Avonex. In addition, neurologic disability as measured by the EDSS did not worsen in 86% of Copaxone patients. The drug is already approved in 44 countries worldwide.
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