UCB seeks label extension for epilepsy agent Briviact

20 January 2017

Belgian drugmaker UCB (Euronext: UCB) has filed a supplemental New Drug Application (sNDA) with the US Food and Drug Administration to extend the label for epilepsy drug Briviact (brivaracetam).

The FDA approved Briviact in February 2016 as an adjunctive therapy in the treatment of partial-onset seizures in epilepsy patients over the age of 16.

If the sNDA is approved, UCB will be able to market the drug as a monotherapy for this indication.

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