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A Trial of the Safety and Tolerability of SEP-363856 in Adults With Generalized Anxiety Disorder
Sponsor: Otsuka Pharmaceutical Development & Commercialization, Inc.
Summary
This is a global, Phase 3, multicenter, open-label extension trial designed to evaluate the long-term safety, tolerability and efficacy of SEP-363856 administered at doses of 50 milligrams (mg) or 75 mg per day in adult participants with generalized anxiety disorder (GAD) over a treatment period of 26 weeks.
Official title: A Phase 3, Multicenter, Open-Label Extension Trial to Evaluate the Safety and Tolerability of SEP-363856 in the Treatment of Adults With Generalized Anxiety Disorder
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
1120
Start Date
2026-10-06
Completion Date
2029-06-02
Last Updated
2026-08-26
Healthy Volunteers
No
Conditions
Interventions
SEP-363856
Oral tablet