French specialty pharmaceutical group says that its drug Dysport (abobotulinumtoxinA for Injection) is now available in the USA for the treatment of cervical dystonia in adults and announced positive findings with its diabetes drug taspoglutide.
Used in patient care in the UK since 1991, Dysport has marketing authorizations in 75 countries (as of December 31, 2008) for multiple therapeutic uses.
Dysport was approved by the US Food and Drug Administration on April 29 for two separate indications, the treatment of cervical dystonia to reduce the severity of abnormal head position and neck pain in both toxin-naïve and previously treated patients, and the temporary improvement in the appearance of moderate to severe glabellar lines in adults younger than 65 years of age. Ipsen will market the product in the USA for the therapeutic indication of cervical dystonia, while Medicis already markets it for the aesthetic indication.
Roche tests of taspoglutide meet primary endpoints, drug beats Byetta
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