A Trial of the Safety and Tolerability of SEP-363856 in Adults With Generalized Anxiety Disorder
Condition(s) studied
Study 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.
Eligibility
Primary outcome measure(s)
- Number of Participants With Treatment-Emergent Adverse Events (TEAEs), Serious Adverse Events (SAEs), and TEAEs Leading to Discontinuation — Throughout the trial (up to Week 27)
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| Clinical Neuroscience Solutions, LLC | Jacksonville | Florida | Recruiting |
| Basil Clinical | Jamaica | New York | Recruiting |
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Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07786454 on ClinicalTrials.gov ↗ ← All trials in the USA