GSK Epilepsy Treatment Gets FDA Approval

2 June 2009 (Last Updated June 2nd, 2009 18:30)

The US Food and Drug Administration has approved GlaxoSmithKline’s Lamictal XR (lamotrigine) extended-release tablets as a once-a-day therapy for epilepsy patients suffering from partial onset seizures. Lamictal XR has been approved as an add-on therapy for adult and adolescent patients

The US Food and Drug Administration has approved GlaxoSmithKline’s Lamictal XR (lamotrigine) extended-release tablets as a once-a-day therapy for epilepsy patients suffering from partial onset seizures.

Lamictal XR has been approved as an add-on therapy for adult and adolescent patients who experience partial seizures with or without secondary generalisation.

GlaxoSmithKline chairman Dean Naritoku said that many patients required multiple doses of one or more medications to control their epilepsy.

“This made taking their medicines even more challenging. Lamictal XR is a once-daily advance for patients with epilepsy who still experience seizures while taking their current therapy," said Naritokou.

Lamictal XR reduced the frequency of partial seizures during a 19-week study.