Tuesday, March 3, 2009

Copaxone Approved by the FDA for Patients with a First Clinical Event Suggestive of Multiple Sclerosis

Mar 3, 2009 - Teva Pharmaceutical Industries Ltd., today announced that the U.S. FDA has approved an expanded indication for COPAXONE (glatiramer acetate injection) to include the treatment of patients who have experienced a first clinical episode and have magnetic resonance imaging features consistent with multiple sclerosis (MS).

the details can be read here.

No comments: