Skip to content
Active, not recruitingPhase 3

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

NCT05711940 · COMPASS Pathways

Closed to entry
Status
Not accepting participants
Phase 3
Phase
572
Target enrolment
116
Study sites
17 US states

What it is testing

Summary

Efficacy, Safety, and Tolerability of two administrations 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 COMP360 1 mg 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: 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

116 study sites

FacilityCityRegionCountry
Lighthouse Psychiatry ScottsdaleGilbertArizonaUnited States
Clinical Innovations, Inc.BellflowerCaliforniaUnited States
M3 Wake ResearchEncinoCaliforniaUnited States
The Regents of the University of California - San DiegoLa JollaCaliforniaUnited States
Kadima Neuropsychiatry InstituteLa JollaCaliforniaUnited States
CalNeuro Research Group, IncLos AngelesCaliforniaUnited States
Catalina Research Institute, LLCMontclairCaliforniaUnited States
Piedmont Hospital Neuroscience CentreOaklandCaliforniaUnited States
ATP Clinical Research, Inc.OrangeCaliforniaUnited States
CITrialsRiversideCaliforniaUnited States
Lumos Clinical Research CenterSan JoseCaliforniaUnited States
Syrentis Clinical ResearchSanta AnaCaliforniaUnited States
Stanford UniversityStanfordCaliforniaUnited States
ASCLEPES Research CentersThousand OaksCaliforniaUnited States
Pacific Clinical Research Management Group, LLCUplandCaliforniaUnited States
Innovative Clinical Research, Inc.LauderhillFloridaUnited States
Central Miami Medical Institute, LLCMiamiFloridaUnited States
Behavioral Clinical Research, Inc.Miami LakesFloridaUnited States
Health Synergy Clinical ResearchOkeechobeeFloridaUnited States
Clinical Neurosciecne Solutions, Inc. dba CNS HealthcareOrlandoFloridaUnited States
APG Research, LLC- Advanced Psychiatric GroupOrlandoFloridaUnited States
University South FloridaTampaFloridaUnited States
Stedman Clinical TrialsTampaFloridaUnited States
Health Synergy Clinical Research, LLCWest Palm BeachFloridaUnited States
Atlanta Center for Medical ResearchAtlantaGeorgiaUnited States
iResearch AtlantaDecaturGeorgiaUnited States
Rush University Medical CenterChicagoIllinoisUnited States
Uptown Research Institute, LLCChicagoIllinoisUnited States
Psychiatric Medicine AssociatesSkokieIllinoisUnited States
Harvard Medical School - McLean HospitalBelmontMassachusettsUnited States
Adams Clinical - Boston (Copley Clinical)BostonMassachusettsUnited States
University of Massachusetts Medical SchoolNorth WorcesterMassachusettsUnited States
Adams Clinical - BostonWatertownMassachusettsUnited States
Michigan Clinical Research Institute PCAnn ArborMichiganUnited States
University Of Michigan Comprehensive Depression CenterAnn ArborMichiganUnited States
Institute for Integrative TherapiesEden PrairieMinnesotaUnited States
St. Charles Psychiatric Associates - Midwest Research GroupSaint CharlesMissouriUnited States
Alivation Research, LLC.LincolnNebraskaUnited States
Hassman Research InstituteBerlinNew JerseyUnited States
Princeton Medical InstitutePrincetonNew JerseyUnited States
Bio Behavioral HealthToms RiverNew JerseyUnited States
Dent Neurosciences Research Center, Inc.AmherstNew YorkUnited States
Fieve Clinical Research, IncNew YorkNew YorkUnited States
Spectrum Neuroscience and Treatment InstituteNew YorkNew YorkUnited States
Adams Clinical - New YorkNew YorkNew YorkUnited States
New York State Psychiatric InstituteNew YorkNew YorkUnited States
Richmond Behavioral AssociatesStaten IslandNew YorkUnited States
Adams Clinical - New YorkThe BronxNew YorkUnited States
University of Cincinnati, Department of Psychiatry & Behavirol NeuroscienceCincinnatiOhioUnited States
Cleveland Clinic - Lutheran HospitalClevelandOhioUnited States
The Ohio State UniversityColumbusOhioUnited States
Suburban Research AssociatesMediaPennsylvaniaUnited States
The University of Texas at Austin - Dell Medical SchoolAustinTexasUnited States
Houston Clinical Trials, LLCBellaireTexasUnited States
Relaro Medical TrialsDallasTexasUnited States
Center for Depression Research and Clinical CareDallasTexasUnited States
North Texas Clinical TrialsFort WorthTexasUnited States
Brain Health Consultants and TMS CenterHoustonTexasUnited States
HCA Healthcare Research Institute - Medical City Green Oaks HospitalPlanoTexasUnited States
Cedar Clinical ResearchDraperUtahUnited States
The University of Utah - Huntsman Mental Health InstituteSalt Lake CityUtahUnited States
Seattle Neuropsychiatric Treatment CenterSeattleWashingtonUnited States
Diex Recherche Sherbrooke Inc.QuébecB.C.Canada
Medical Arts Health Research Centre, KamloopsKamloopsBritish ColumbiaCanada
Okanagan Clinical TrialsKelownaBritish ColumbiaCanada
Medical Arts Research Group - PentictonPentictonBritish ColumbiaCanada
Chatham-Kent Clnical Trials CentreChathamOntarioCanada
St. Michael's HospitalTorontoOntarioCanada
Centre for Addiction and Mental Health (CAMH)TorontoOntarioCanada
Centre for Neurology StudiesVancouverCanada
Medical Arts Research GroupVancouverCanada
National Institute of Mental HealthKlecanyCzechia
Neuroterapie KH SroKutná HoraCzechia
Psychiatric AmbulanceOstravaCzechia
A-Shine s.r.o.PilsenCzechia
Psychedelicka klinika, s.r.o.PragueCzechia
Institut Neuropsychiatricke PecePragueCzechia
Aalborg Universitetshospital-Psykiatrien Region NordjyllandAalborgDenmark
Ghu-Centre Hospitalier Sainte Anne, Centre de Recherche CliniqueParisParisFrance
Centre Hospitalier Universitaire de Nimes (CHU) - Hopital Universitaire CaremeauNîmesFrance

Showing the first 80 of 116

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.

Before you do, the preparation checklist lists what a site will ask you on a first call and what is worth asking them. It is free and collects nothing.

NCT05711940 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