S-P's Bridion gets nod from EMEA's CHMP

8 June 2008

US drug major Schering-Plough says that the European Medicines Agency's (EMEA) Committee for Medicinal Products for Human Use (CHMP) has recommended the approval of Bridion (sugammadex) for routine reversal of the muscle relaxants rocuronium or vecuronium and for immediate reversal of rocuronium in adults, and for routine reversal following rocuronium in children and adolescents.

The agent, which was the star acquisition from S-P's $16.3 billion takeover of Organon BioSciences (Marketletter November 26, 2007), could transform the practice of anesthesia through improved management of muscle relaxation in the millions of surgeries where rocuronium and vecuronium are used. A Food and Drug Administration advisory committee recommended the agent earlier this year (Marketletter March 17).

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