UCB Group Release: A Key Regulatory Milestone For Keppra(R)

BRUSSELS, BELGIUM--(MARKET WIRE)--Jul 3, 2006 -- UCB today announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMEA) has issued a positive opinion to approve marketing authorisation of Keppra® (levetiracetam) as monotherapy in the treatment of partial onset seizures with or without secondary generalisation in patients from 16 years of age with newly diagnosed epilepsy.
MORE ON THIS TOPIC