FDA nod to UCB’s Vimpat as an add-on therapy for epilepsy
The U.S. Food and Drug Administration has given the approval to UCB’s Vimpat® (lacosamide) for use as an adjunct therapy in the treatment of partial-onset seizures in epilepsy patients older than 17 years of age. The novel anti-epileptic drug has an innovative mechanism of action which involves the modulation of activity of sodium channels in the nervous system. It prolongs the long-lasting resting condition of the channel, thereby controlling the hyperactive nerve cells.
- Bayer develops thinnest needle for MS
- NICE recommends SCS for spine pain management
- Genentech submits sBLA for Avastin’s use in glioblastoma treatment
- JV formed to develop treatment for peripheral nerve injury
