EXTON, Pa.--(BUSINESS WIRE)--Adolor Corporation (Nasdaq:ADLR) announced today that the U.S. Food and Drug Administration (FDA) has posted on its website briefing documents for the scheduled Gastrointestinal Drugs Advisory Committee (GIDAC) meeting to review Adolor’s New Drug Application (NDA) for Entereg® (alvimopan) for the proposed indication of acceleration of time to upper and lower gastrointestinal recovery following partial large or small bowel resection surgery with primary anastomosis.
