Orphan Medical has licensed European sales and marketing rights forXyrem (sodium oxybate) oral solution to UK-based Celltech. Orphan received US Food and Drug Administration approval in July 2002 to market Xyrem as a treatment for cataplexy (a chronic neurological disorder characterized by sudden episodes of muscle weakness triggered by emotional changes) in patients with narcolepsy.
Celltech has indicated that it expects to file an Xyrem Marketing Authorization Application for the cataplexy indication in Europe in early 2004 and, upon approval, will use its specialist sales forces to market the product to the target audience of neurologists and sleep specialists.
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