Story thread · 3 reports / 3 sources
U.S. FDA Accepts Teva’s New Drug Application (NDA) and Grants Priority Review for Ecopipam, a First-in-Class Investigational Therapy for Pediatric Patients with Tourette Syndrome
markets.businessinsider.com · 2h · first report
Ecopipam (EBS-101) is a first-in-class selective D1 (dopamine) receptor antagonist with Orphan Drug designation NDA acceptance is supported by positive Phase 3 data, which were published in JAMA Neurology, and Phase 2b...
The coverage
- Teva gets FDA priority review for Tourette syndrome therapy
seekingalpha.com · 2h
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