US drugmaker Talecris Biotherapeutics has highlighted the publication of results from a trial of Gamunex (immune globulin intravenous [human], 10% caprylate/chromatography purified) in patients with chronic inflammatory demyelinating polyneuropathy in the journal Neurology. The analysis of the randomized, placebo-controlled ICE study showed that patients who received Gamunex experienced greater improvements in physical and mental component scores compared with placebo. Gamunex is the first and only Food and Drug Administration-approved product for the treatment of CIDP.
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
| Headless Content Management with Blaze