MARIETTA, Ga., April 1 /PRNewswire/ -- As announced last week during a corporate press conference in Brussels, Solvay Pharmaceuticals, Inc. has received a letter from the Food and Drug Administration (FDA) on its new drug application (NDA) for cilansetron, a novel drug submitted to the Agency for the treatment of irritable bowel syndrome with diarrhea predominance (IBS-D) in both men and women. The "not-approvable" action letter requests additional clinical trials. Solvay Pharmaceuticals, Inc. is examining its options and will discuss future steps with the FDA and other experts for this product in the U.S.
As many as 30-45 million North American adults have symptoms of IBS -- approximately one-third from IBS-D. The common symptoms of IBS-D are diarrhea, abdominal pain/discomfort, and fecal urgency. IBS has a significant negative impact on the quality of life for the many men and women who suffer from this condition, causing lost days of work and interfering with home- based, social and leisure activities.
About Solvay Pharmaceuticals, Inc.
Solvay Pharmaceuticals, Inc. (http://www.solvaypharmaceuticals-us.com/) of Marietta, Georgia (USA), is a research-driven pharmaceutical company that seeks to fulfill unmet medical needs in the therapeutic areas of cardiology, gastroenterology, mental health, women's health and a select group of specialized markets including men's health. It is a part of the global Solvay Pharmaceuticals organization whose core activities consist of discovering, developing and manufacturing medicines for human use. Solvay Pharmaceuticals, Inc. is a subsidiary corporation of the worldwide Solvay Group of chemical and pharmaceutical companies headquartered in Brussels, Belgium.
Solvay Pharmaceuticals, Inc.
CONTACT: Gabrielle Braswell, Assistant Director, Public Affairs, ofSolvay Pharmaceuticals, Inc., +1-770-578-5637, email@example.com