Sunovion Pharmaceuticals Inc., the US subsidiary of Sumitomo Dainippon Pharma Co. Ltd. in Japan, had forged ahead with a new drug application (NDA) for its novel non-stimulant attention deficit/hyperactivity disorder (ADHD) drug dasotraline after having mixed clinical results, but the effort has failed with the Aug. 31 announcement of a complete response letter from the US FDA.
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Scrip for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?