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Study identifier: NCT05593029 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: Completed

A Trial of the Safety and Efficacy of SEP-363856 in the Treatment of Adults With Major Depressive Disorder

Condition: Major Depressive Disorder  ·  Sponsor: Otsuka Pharmaceutical Development & Commercialization, Inc.

PhasePhase 2
Planned participants929
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNoCheck eligibility criteria ↓
Where77 locations · 7 countries

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

Demonstrate ability of SEP-363856 to be superior to placebo as an adjunctive therapy to ADT in change from baseline in depressive symptoms (MADRS \& CGI-S) in MDD patients who had an inadequate response to prior ADT therapy.

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * Male and Female subjects between 18-65 years of age, with a primary diagnosis of major depressive disorder and in a current major depressive episode * Current major depressive episode must be at least 8 weeks and no longer than 2 years in duration * History of an inadequate response to at least 1 and no more than 3 antidepressant treatments in the current major depressive episode Exclusion Criteria: * Subjects who report an inadequate response to more than 3 antidepressant treatments in the current episode * Subjects with a lifetime history of schizophrenia spectrum or other psychotic disorder, bipolar or related disorder, major or mild neurocognitive disorder, neurodevelopmental disorder of greater than mild severity or of a severity that impacts the participant's ability to consent/ follow study directions/ or otherwise safely participate in the study, borderline or antisocial personality disorder. * Subjects with a current diagnosis of post-traumatic stress disorder, obsessive compulsive disorder, panic disorder, or eating disorder (including anorexia nervosa or bulimia). * Sexually active subjects, who could become pregnant, not agreeing to practice 2 sponsor approved methods of birth control or remain abstinent during the trial and for 30 days (females) or 90 days (males) after last dose of study drug.

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (77)

University of Alabama at BirminghamBirmingham, Alabama, United States
Scottsdale Clinical ResearchScottsdale, Arizona, United States
DelSol ResearchTucson, Arizona, United States
Pillar Clinical ResearchBentonville, Arkansas, United States
ProScience Research GroupCulver City, California, United States
Wr-Pri, LlcEncino, California, United States
Collaborative NeuroScience Research , LLCGarden Grove, California, United States
Alliance ResearchLong Beach, California, United States
ATP Clinical Research, Inc.Orange, California, United States
Anderson Clinical ResearchRedlands, California, United States
California Mental Behavioral HealthSantee, California, United States
Schuster Medical Research Institute SMRISherman Oaks, California, United States

+ 65 more locations — full list on the registry record.

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

BirminghamScottsdaleTucsonBentonville

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