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

  1. Teva gets FDA priority review for Tourette syndrome therapy

    seekingalpha.com · 2h

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