Login to Your Account

Santhera Withdraws Raxone MAA, Plans Resubmission

By Cormac Sheridan
Staff Writer

Monday, March 25, 2013
With additional data in the offing for its Leber's Hereditary Optic Neuropathy (LHON) drug Raxone (idebenone), Santhera Pharmaceuticals AG has withdrawn its marketing authorization application (MAA) from the European Medicines Agency's (EMA) re-examination process and will instead submit a new file with an expanded patient database.

To continue reading subscribe now to BioWorld Today

Learn More about BioWorld Today

Already a subscriber? Sign In or Buy now to activate your subscription