Germany's Schering AG says that its multiple sclerosis drug Betaferon (interferon beta-1b, marketed as Betaseron in Canada by Schering's affiliate Berlex Canada), has been granted marketing authorization by the Health Products and Food Branch of Health Canada for an extension of its indication to include the treatment of patients with a first clinical event suggestive of MS.
Schering noted that, with this clearance, the agent becomes the highest-dose highest-frequency therapy approved for the treatment of the earliest stages of MS in Canada, adding that the approval provides an important therapy option for patients to reduce the risk of developing clinically-definite MS, as well as the potential to delay disease progression.
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
Sign up to receive email updates
Join industry leaders for a daily roundup of biotech & pharma news
Copyright © The Pharma Letter 2025 | Headless Content Management with Blaze