What this study is
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).
What's being tested
- SEP-363856
Intervention · DRUG
- Placebo
Intervention · DRUG
Both interventions
Oral tablet
Study details
- 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
- Sponsor
- Otsuka Pharmaceutical Development & Commercialization, Inc.
- Conditions
- Generalized Anxiety Disorder
- Enrolling
- 384 people
- Starts
- 2026-08-06
- Est. completion
- 2028-11-01
- Design
- Triple-blind, randomized, parallel groups, Phase 3
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 18 Years and overSex ALLHealthy volunteers Not acceptedYou may qualify if
- Male or female participants at least 18 years of age at the time of informed consent
- Primary diagnosis of GAD per Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5), confirmed by Mini-International Neuropsychiatric Interview (MINI) and clinical psychiatric evaluation
- Body Mass Index (BMI) 18-40 kilograms per square meter (kg/m^2)
- Participant is willing and able to comply with study procedures and visit schedule
- Medically stable as determined by medical history, physical exam, vital signs, and laboratory tests and able to comply with study procedures
- Willing and able to discontinue prohibited medications/therapies per protocol
- (i ) Females of childbearing potential: negative pregnancy test and agreement to use acceptable contraception (ii) Males: agreement to follow protocol-defined contraception and reproductive restrictions
- Willing and able to discontinue prohibited medications/therapies per protocol
You can't join if
- Current DSM-5 diagnosis of major depressive episode, post traumatic stress disorder (PTSD), or any psychiatric disorder other than GAD that was the primary focus of treatment within 12 months prior to screening
- Substance use disorder (excluding nicotine/caffeine) within 12 months prior to screening
- Lifetime history of certain psychiatric disorders (e.g., schizophrenia spectrum disorders, bipolar disorder, obsessive-compulsive disorder, borderline or antisocial personality disorder)
- Significant suicide risk e.g., recent suicidal behavior/ideation per Columbia-Suicide Severity Rating Scale [C-SSRS] or MADRS)
- Use of prohibited medications/therapies within protocol-defined timeframes (e.g., certain antipsychotics, mood stabilizers, benzodiazepines, investigational treatments)
- Prior exposure to restricted treatments
- Pregnant or breastfeeding females
- Participation in another investigational study within 180 days (or more than [>] 1 trial in last year)
- Known history of human immunodeficiency virus seropositivity, hepatitis B or C
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (11)
11 openContact for every open site
- Otsuka Call Center · Contact844-687-8522Otsuka-ProfessionalServices@otsuka-us.com
Anderson Clinical Research
Redlands, California, United States
- Anderson · Principal investigator
RecruitingClinical Neuroscience Solutions Inc. (CNS) - Orlando
Orlando, Florida, United States
- Molpus · Principal investigator
RecruitingAdams Clinical - Watertown
Watertown, Massachusetts, United States
- Ellickson · Principal investigator
RecruitingLumina Clinical Research Center
Cherry Hill, New Jersey, United States
- Corcoran · Principal investigator
RecruitingBasil Clinical
Jamaica, New York, United States
- Rapp · Principal investigator
RecruitingIMA Clinical Research NYC Uptown
New York, New York, United States
- Careri · Principal investigator
RecruitingSummit Research Network
Portland, Oregon, United States
- Essink · Principal investigator
RecruitingAdams Clinical Philadelphia
Philadelphia, Pennsylvania, United States
- Blanchard · Principal investigator
RecruitingCNS Healthcare - Memphis
Memphis, Tennessee, United States
- Arnold · Principal investigator
RecruitingDM Clinical Research - Bellaire
Houston, Texas, United States
- Karakoc · Principal investigator
RecruitingCore Clinical Research
Everett, Washington, United States
- Knutson · Principal investigator
Recruiting
Study team
Sponsor
Otsuka Pharmaceutical Development & Commercialization, Inc.
Study ID 382-201-00033
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.