Merck Statement on FDA Advisory Committee Meeting About Sugammadex Sodium Injection

Dateline City:  WHITEHOUSE STATION, N.J. WHITEHOUSE STATION, N.J.--(BUSINESS WIRE)--Merck (NYSE: MRK), known as MSD outside the United States and Canada, confirmed today that the U.S. Food and Drug Administration (FDA) has cancelled Thursday’s discussion of sugammadex at the Anesthetic and Analgesic Drug Products Advisory Committee (AADPAC). Sugammadex sodium injection is Merck’s investigational medicine for the reversal of neuromuscular blockade (NMB) induced by rocuronium or vecuronium. Language:  English Contact:  MerckMedia:Pam Eisele, 908-423-5042Sarra Herzog, 908-423-6154orInvestors:Carol Ferguson, 908-423-4465Justin Holko, 908-423-5088 Ticker Slug:  Ticker: MRK Exchange: NYSE read more
Source: Merck.com - Research and Development News - Category: Pharmaceuticals Authors: Tags: Research and Development News Corporate News Latest News Source Type: news