The FDA DBRUP and the DGIEP accepted the INDs for the treatment of overactive bladder and iIBS, respectively.
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[17-January-2018] |
INDIANAPOLIS and LONDON, Jan. 17, 2018 /PRNewswire/ -- Outpost Medicine, a biopharmaceutical company focused on the development of new treatments of urologic and gastrointestinal disorders, today announced that the U.S. Food and Drug Administration (FDA) has accepted two Investigational New Drug (IND) applications for its lead product candidate, OP-687. The FDA Division of Bone, Reproductive and Urologic Products (DBRUP) and the Division of Gastroenterology and Inborn Errors Products (DGIEP) accepted the INDs for the treatment of overactive bladder (OAB) and irritable bowel syndrome (IBS), respectively. “The acceptance of these INDs is an important milestone for the OP-687 program, allowing us to immediately initiate clinical testing,” said Scott Byrd, Chief Executive Officer of Outpost. “We are excited about the possibilities for this first-in-class treatment for OAB and IBS and are now well positioned to rapidly advance the clinical program.” “Current treatments for OAB and IBS have significant limitations in terms of both efficacy and tolerability, resulting in high rates of treatment failure,” commented Dr. Ian Mills, Chief Medical Officer. “We believe OP-687 has the potential to meaningfully improve care for millions of patients suffering from these serious disorders.” About Overactive Bladder About Irritable Bowel Syndrome About Outpost Medicine Contact:
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