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EU recommends Rebif new formulation for MS patients

Sunday, July 1, 2007

Merck KGaA announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMEA) has issued a positive opinion recommending marketing authorization of a new formulation of Rebif (interferon beta-1a) for the treatment of relapsing multiple sclerosis (MS).
From: www.pharmabiz.com

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