NPS Pharma (NPSP) Submits CMC of NDA for GATTEX to U.S. FDA
Get Alerts NPSP Hot Sheet
Join SI Premium – FREE
NPS Pharmaceuticals, Inc. (Nasdaq: NPSP), has submitted the chemistry, manufacturing and controls (CMC) section of its new drug application (NDA) for GATTEX (teduglutide) to the U.S. Food and Drug Administration (FDA).
GATTEX is a novel, recombinant analog of human glucagon-like peptide 2 that the company is developing for the treatment of adults with short bowel syndrome or SBS.
GATTEX is a novel, recombinant analog of human glucagon-like peptide 2 that the company is developing for the treatment of adults with short bowel syndrome or SBS.
Serious News for Serious Traders! Try StreetInsider.com Premium Free!
You May Also Be Interested In
- Sky Quarry names Heidi Bowman as CFO
- Scholar Rock updates apitegromab regulatory status in U.S., Europe, Japan
- Robo.ai names Hao Wang of Changer.ae to its board of directors
Create E-mail Alert Related Categories
Corporate News, FDASign up for StreetInsider Free!
Receive full access to all new and archived articles, unlimited portfolio tracking, e-mail alerts, custom newswires and RSS feeds - and more!



Tweet
Share