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Recruiting Phase 3

A Trial of the Efficacy and Safety of a Fixed Dose of SEP-363856 in Adults With Generalized Anxiety Disorder

NCT07767903 · tracked via the Priya Life Science USA tracker
Phase
Phase 3
Started
2026-08-06
Last updated
2026-10-20

Condition(s) studied

Generalized Anxiety Disorder

Investigational drug(s) / intervention(s)

SEP-363856 →Placebo

SEP-363856: Oral tablet

Placebo: Oral tablet

Study 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).

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Key Inclusion Criteria 1. Male or female participants at least 18 years of age at the time of informed consent 2. 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 3. Body Mass Index (BMI) 18-40 kilograms per square meter (kg/m\^2) 4. Participant is willing and able to comply with study procedures and visit schedule 5. Medically stable as determined by medical history, physical exam, vital signs, and laboratory tests and able to comply with study procedures 6. Willing and able to discontinue prohibited medications/therapies per protocol 7. (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 8. Willing and able to discontinue prohibited medications/therapies per protocol Key Exclusion Criteria 1. 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 2. Substance use disorder (excluding nicotine/caffeine) within 12 months prior to screening 3. Lifetime history of certain psychiatric disorders (e.g., schizophrenia spectrum disorders, bipolar disorder, obsessive-compulsive disorder, borderline or antisocial personality disorder) 4. Significant suicide risk e.g., recent suicidal behavior/ideation per Columbia-Suicide Severity Rating Scale \[C-SSRS\] or MADRS) 5. Use of prohibited medications/therapies within protocol-defined timeframes (e.g., certain antipsychotics, mood stabilizers, benzodiazepines, investigational treatments) 6. Prior exposure to restricted treatments 7. Pregnant or breastfeeding females 8. Participation in another investigational study within 180 days (or more than \[\>\] 1 trial in last year) 9. Known history of human immunodeficiency virus seropositivity, hepatitis B or C

Primary outcome measure(s)

  • Change From Baseline at Week 8 in Hamilton Anxiety Rating Scale (HAM-A) Total Score — Baseline, Week 8
    The HAM-A is a clinician-administered rating scale developed to quantify the severity of anxiety symptomatology. It consists of 14 items, each defined by a series of symptoms. Each item is scored on a 5-point Likert-type scale ranging from 0 (absent) to 4 (very severe). The total score ranges from 0 to 56, with higher scores indicating greater severity.

Trial sites (11)

FacilityCityRegionStatus
Anderson Clinical Research Redlands California Recruiting
Clinical Neuroscience Solutions Inc. (CNS) - Orlando Orlando Florida Recruiting
Adams Clinical - Watertown Watertown Massachusetts Recruiting
Lumina Clinical Research Center Cherry Hill New Jersey Recruiting
Basil Clinical Jamaica New York Recruiting
IMA Clinical Research NYC Uptown New York New York Recruiting
Summit Research Network Portland Oregon Recruiting
Adams Clinical Philadelphia Philadelphia Pennsylvania Recruiting
CNS Healthcare - Memphis Memphis Tennessee Recruiting
DM Clinical Research - Bellaire Houston Texas Recruiting
Core Clinical Research Everett Washington Recruiting
Official registry record

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 NCT07767903 on ClinicalTrials.gov ↗ ← All trials in the USA