EU agency recommends UCB’s Keppra for child use

Belgian drug maker UCB said on Monday a European committee had approved the use of its Keppra drug on children four years of age and older suffering from epilepsy.

The Committee for Medicinal Products for Human Use of the European Medicines Agency (EMEA) had issued a positive opinion, recommending approval of the drug as adjunctive therapy in the treatment of partial-onset Seizures, it said in a statement. EMEA would forward the recommendation to the European Commission for review and final decision, which is expected within 90 days, it said.

In June, the U.S. Food and Drug Administration approved the paediatric indication for Keppra under priority review.

UCB shares were up 1.37 percent at 45.09 euros, by 0823 GMT.

Provided by ArmMed Media
Revision date: June 18, 2011
Last revised: by Amalia K. Gagarina, M.S., R.D.