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A Trial of the Efficacy and Safety of a Fixed Dose of SEP-363856 in Adults With Generalized Anxiety Disorder
Sponsor: Otsuka Pharmaceutical Development & Commercialization, Inc.
Summary
This is a global, phase 3, randomized, double-blind, parallel-group, 2-arm, placebo controlled, multicenter trial designed to compare the efficacy, safety and tolerability of a fixed dose of SEP-363856 (75 millligrams per day \[mg/day\]) to placebo over an 8-week double-blind treatment period in adults with generalized anxiety disorder (GAD).
Official title: A Phase 3, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled, Multicenter Trial to Compare the Efficacy and Safety of a Fixed Dose of SEP-363856 to Placebo in the Treatment of Adults With Generalized Anxiety Disorder
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
384
Start Date
2026-08-06
Completion Date
2028-11-01
Last Updated
2026-10-20
Healthy Volunteers
No
Conditions
Interventions
SEP-363856
Oral tablet
Placebo
Oral tablet
Locations (11)
Anderson Clinical Research
Redlands, California, United States
Clinical Neuroscience Solutions Inc. (CNS) - Orlando
Orlando, Florida, United States
Adams Clinical - Watertown
Watertown, Massachusetts, United States
Lumina Clinical Research Center
Cherry Hill, New Jersey, United States
Basil Clinical
Jamaica, New York, United States
IMA Clinical Research NYC Uptown
New York, New York, United States
Summit Research Network
Portland, Oregon, United States
Adams Clinical Philadelphia
Philadelphia, Pennsylvania, United States
CNS Healthcare - Memphis
Memphis, Tennessee, United States
DM Clinical Research - Bellaire
Houston, Texas, United States
Core Clinical Research
Everett, Washington, United States