A Clinical Study That Will Measure How Well SEP-363856 Works and How Safe it is in Adults With Generalized Anxiety Disorder
About the study
A clinical study that will meaure how well SEP-363856 works and how safe it is in adults with Generalized Anixety Disorder. This study will be accepting both male and female subjects between the ages of 18 years and 65 years old. The study will be held in Approximately 50 global study centers and approximately 15 additional centers for a separate Japan population. Participation in the study can be up to approximately 12 weeks.
Who can take part
You may be eligible to participate in the study if you meet the following criteria:
INCLUSION CRITERIA
Inclusion Criteria: (list is not all inclusive)
- Male or female subject between 18 to 65 years of age.
- Subject meets DSM-5 criteria for a diagnosis of Generalized Anxiety Disorder.
- Subject must be willing and able to comply with the study procedures and visit schedule and must be able to understand and follow verbal and written instructions.
EXCLUSION CRITERIA
Exclusion Criteria: (list is not all inclusive)
- Subject has DSM-5-based diagnosis of any disorder other than Generalized Anxiety Disorder that was the primary focus of treatment within 12 months before Screening.
- Subjects who report an inadequate response to more than 3 antidepressant treatments
- Subject is at significant risk of harming self or others based on Investigator's judgment.
- Subject has any clinically significant unstable medical condition or any clinically significant chronic disease that in the opinion of the Investigator, would limit the subject's ability to complete and/or participate in the study.
- Female subject who is pregnant, lactating, or plans to get pregnant during the study.
Study Locations
Enter your ZIP code/Postal code/PIN code to locate study sites near you:
How to Apply
Contact the study center to learn if this study is a good match for you.
Study Details
Contition
Generalized Anxiety Disorder
Age
18+
Phase
PHASE2/PHASE3
Participants Needed
434
Est. Completion Date
Feb 8, 2025
Treatment Type
INTERVENTIONAL
Sponsor
Otsuka Pharmaceutical Development & Commercialization, Inc.
ClinicalTrials.gov NCT Identifier
NCT05729373
Study Number
SEP361-226
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