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CompletedPhase 3

Efficacy, Safety, and Tolerability of COMP360 in Participants With TRD

NCT05624268 · COMPASS Pathways

Closed to entry
Status
Not accepting participants
Phase 3
Phase
258
Target enrolment
40
Study sites
19 US states

What it is testing

Summary

Efficacy, Safety, and Tolerability of a single administration of COMP360 in participants with treatment-resistant depression (TRD)

Summary as written by the trial’s own sponsor and published on ClinicalTrials.gov API v2. It is the sponsor’s description, reproduced unedited, not an assessment by this site.

What counts as success

Primary outcome measures

  • COMP360 25 mg versus placebo for the change from baseline in MADRS total score

    Measured over Week 6

A trial succeeds or fails on its primary outcome, declared in advance. Everything else it reports is secondary by definition.

Who can take part

Eligibility, as published

18 Years
Ages
All
Sex
Not accepted
Healthy volunteers
Key Inclusion Criteria: 1. Aged ≥18 years at Screening 2. Major depression without psychotic features (single or recurrent episode as informed by the Diagnostic and Statistical Manual of Mental Disorders, 5th edition \[DSM-5\]) 3. If the current major depressive episode is the participant's first lifetime episode of depression, the length of the current episode must be ≥3 months and ≤2 years at Screening 4. MADRS total score ≥20 at Screening and Baseline to ensure at least moderate severity of depression 5. TRD, defined as failure to respond to an adequate dose and duration of two, three, or four different pharmacological treatments for the current episode as determined through the Massachusetts General Hospital Antidepressant Treatment Response Questionnaire (MGH-ATRQ) and using the supplementary advice on additional antidepressants not included in MGH-ATRQ. 6. At Screening, agreement to discontinue all prohibited medications. Key Exclusion Criteria: Psychiatric Exclusion Criteria: 1. Prior or ongoing bipolar disorder, any psychotic disorder, including schizophrenia, schizophreniform disorder, schizoaffective disorder, brief psychotic disorder (unless substance induced or due to a medical condition), antisocial personality disorder as assessed by a structured clinical interview (MINI 7.0.2) 2. Lifetime paranoid, schizoid, schizotypal, histrionic, narcissistic personality disorder, or any ongoing serious psychiatric comorbidity based on medical history and clinical judgement 3. Borderline personality disorder as demonstrated by medical history or the Mini International Neuropsychiatric Interview Plus (MINI plus) - borderline personality disorder module 4. Ongoing post-traumatic stress disorder, obsessive-compulsive disorder, or anorexia nervosa as assessed by medical history and a structured clinical interview (MINI 7.0.2) 5. Psychiatric inpatient within the past 12 months prior to Screening 6. Use of electroconvulsive therapy, deep brain stimulation, or vagus nerve stimulation during the current depressive episode 7. Transcranial magnetic stimulation within the past six months prior to Screening 8. Current enrolment in a psychological therapy programme that will not remain stable for the duration of the study. Psychological therapies cannot have been initiated within 30 days prior to Screening 9. Exposure to COMP360 psilocybin therapy prior to Screening

Where

40 study sites

FacilityCityRegionCountry
University of Arizona College of Medicine - TusconTusconArizonaUnited States
ProScience Research GroupCulver CityCaliforniaUnited States
Collaborative Neuroscience Network, LLCGarden GroveCaliforniaUnited States
Kadima Neuropsychiatry InstituteLa JollaCaliforniaUnited States
University California San DiegoLa JollaCaliforniaUnited States
California Center for Psychedelic TherapyLos AngelesCaliforniaUnited States
CalNeuro Research Group, IncLos AngelesCaliforniaUnited States
Clarity Clinical Research, LLCLos AngelesCaliforniaUnited States
ATP Clinical Research, Inc.OrangeCaliforniaUnited States
Artemis Institute for Clinical ResearchSan DiegoCaliforniaUnited States
Lumos Clinical Research CenterSan JoseCaliforniaUnited States
Stanford UniversityStanfordCaliforniaUnited States
ASCLEPES Research CentersThousand OaksCaliforniaUnited States
Comprehensive Psychiatric CareNorwichConnecticutUnited States
Clinical Neurosciecne Solutions, Inc. dba CNS HealthcareOrlandoFloridaUnited States
APG Research, LLCOrlandoFloridaUnited States
DMI Health Care Group, IncTampaFloridaUnited States
Meridien Research/Accel ResearchTampaFloridaUnited States
Psych AtlantaAtlantaGeorgiaUnited States
Emory UniversityAtlantaGeorgiaUnited States
Uptown Research Institute, LLCChicagoIllinoisUnited States
Sheppard Pratt Health SystemBaltimoreMarylandUnited States
CBH Health, LLCGaithersburgMarylandUnited States
Pharmasite Research, IncPikesvilleMarylandUnited States
University of Massachusetts Medical SchoolNorth WorcesterMassachusettsUnited States
University of MinnesotaMinneapolisMinnesotaUnited States
University of MissouriColumbiaMissouriUnited States
Midwest Research GroupSaint CharlesMissouriUnited States
Washington University School of MedicineSt LouisMissouriUnited States
Alivation Research, LLC.LincolnNebraskaUnited States
Bio Behavioral HealthToms RiverNew JerseyUnited States
New York State Psychiatric InstituteNew YorkNew YorkUnited States
The Medical Research Network, LLCNew YorkNew YorkUnited States
Insight Clinical Trials, LLCBeachwoodOhioUnited States
Neuro-Behaviroral Clinical Research, Inc.North CantonOhioUnited States
Rivus Wellness & Research InstituteOklahoma CityOklahomaUnited States
Global Medical Institutes, LLC, Scranton Medical InstituteMoosicPennsylvaniaUnited States
UT Health Science Center at Houston (UTHSC-H)HoustonTexasUnited States
Cedar Clinical ResearchDraperUtahUnited States
Core Clinical ResearchEverettWashingtonUnited States

On the registry

Contact the trial directly

This site does not enrol anyone and is not involved in this trial. To ask about taking part, use the sponsor’s own contact details on the official registry record, which is also where the most current version of everything above lives.

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NCT05624268 on ClinicalTrials.gov →

Last updated in the registry 2026-08-10. Registry records change; this page reflects the data build of 2026-08-25.

Related

Where this trial sits