Ground Hog Day For Merck: FDA Again Cancels Sugammadex Advisory Committee Review

FDA is conducting additional inspections of the site of a hypersensitivity study the agency requested in 2008; concerns about the study derailed a committee review in 2013.

In a repeat of what occurred in 2013, FDA has suddenly cancelled an advisory committee meeting scheduled to review Merck & Co. Inc.’s anesthesia reversal agent sugammadex.

The agency informed Merck on March 13 that it had cancelled a meeting of the Anesthetic and Analgesic Drug Products

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