Sanofi (Euronext: SAN) has published six-year investigational data on its Multiple Sclerosis (MS) drug Lemtrada (alemtuzumab) showing that most patients experienced sustained effects of treatment on disease activity despite receiving their last treatment course five years previously.
Sanofi Genzyme, the French pharma major's specialty care global business, presented the results at the European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS).
Lemtrada, a humanized monoclonal antibody, was granted European Union marketing authorization in September 2013 to treat adult patients with active relapsing remitting multiple sclerosis (RRMS) defined by clinical or imaging features.
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