Belgian pharmaceutical company UCB (Euronext Brussels: UCB) has announced that the US Food and Drug Administration has green-lit the company’s application to extend the marketable use of Briviact (brivaracetam).
The drug, which was approved as an adjunctive therapy against partial-onset seizures (POS) in early 2016, is now indicated as monotherapy for this condition.
Briviact is the newest antiepileptic drug in the 'racetam' class of medicines and demonstrates a high and selective affinity for synaptic vesicle protein 2A in the brain, which may contribute to its anticonvulsant effects.
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