Merck KGaA Announces Extension of FDA Priority Review Period for Cladribine Tablets for the Treatment of Relapsing Forms of MS
FDA extends Priority Review period of Cladribine Tablets by three months
Merck KGaA announced that the U.S. food and Drug Administration (FDA) has extended its review period for Cladribine Tablets as a therapy for relapsing forms of multiple sclerosis (MS) by three months to February 28, 2011.
The FDA granted Priority Review status for Cladribine Tablets in July of 2010, reducing the standard 10-month review period to six months, which was set to end on November 28, 2010. The FDA extended the review period to provide additional time for a full review of additional information provided under the new drug application (NDA).
“Merck Serono continues to work closely with the FDA during the review process of the Cladribine Tablets new drug application,” said Bernhard Kirschbaum, Merck Serono’s Head of Global Research and Development. “We will continue working towards our goal of providing an oral disease-modifying drug for the treatment of relapsing multiple sclerosis.”
Other news from the department research and development
