🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in the UK / NCT05711940
Active, not recruiting Phase 3

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

NCT05711940 · tracked via the Priya Life Science UK tracker
Sponsor
COMPASS Pathways
Phase
Phase 3
Started
2023-02-14
Last updated
2026-08-10

Condition(s) studied

Treatment Resistant Depression

Investigational drug(s) / intervention(s)

Psilocybin

Psilocybin: COMP360 Psilocybin administered under supportive conditions

Study summary

Efficacy, Safety, and Tolerability of two administrations of COMP360 in participants with treatment-resistant depression (TRD)

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
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

Primary outcome measure(s)

Trial sites (116)

FacilityCityRegionStatus
Lighthouse Psychiatry Scottsdale Gilbert Arizona
Clinical Innovations, Inc. Bellflower California
M3 Wake Research Encino California
The Regents of the University of California - San Diego La Jolla California
Kadima Neuropsychiatry Institute La Jolla California
CalNeuro Research Group, Inc Los Angeles California
Catalina Research Institute, LLC Montclair California
Piedmont Hospital Neuroscience Centre Oakland California
ATP Clinical Research, Inc. Orange California
CITrials Riverside California
Lumos Clinical Research Center San Jose California
Syrentis Clinical Research Santa Ana California
Stanford University Stanford California
ASCLEPES Research Centers Thousand Oaks California
Pacific Clinical Research Management Group, LLC Upland California
Innovative Clinical Research, Inc. Lauderhill Florida
Central Miami Medical Institute, LLC Miami Florida
Behavioral Clinical Research, Inc. Miami Lakes Florida
Health Synergy Clinical Research Okeechobee Florida
Clinical Neurosciecne Solutions, Inc. dba CNS Healthcare Orlando Florida
APG Research, LLC- Advanced Psychiatric Group Orlando Florida
University South Florida Tampa Florida
Stedman Clinical Trials Tampa Florida
Health Synergy Clinical Research, LLC West Palm Beach Florida
Atlanta Center for Medical Research Atlanta Georgia
iResearch Atlanta Decatur Georgia
Rush University Medical Center Chicago Illinois
Uptown Research Institute, LLC Chicago Illinois
Psychiatric Medicine Associates Skokie Illinois
Harvard Medical School - McLean Hospital Belmont Massachusetts
Adams Clinical - Boston (Copley Clinical) Boston Massachusetts
University of Massachusetts Medical School North Worcester Massachusetts
Adams Clinical - Boston Watertown Massachusetts
Michigan Clinical Research Institute PC Ann Arbor Michigan
University Of Michigan Comprehensive Depression Center Ann Arbor Michigan
Institute for Integrative Therapies Eden Prairie Minnesota
St. Charles Psychiatric Associates - Midwest Research Group Saint Charles Missouri
Alivation Research, LLC. Lincoln Nebraska
Hassman Research Institute Berlin New Jersey
Princeton Medical Institute Princeton New Jersey

+ 76 more sites — see the full list on the official registry below.

Other trials for the same condition

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 NCT05711940 on ClinicalTrials.gov ↗ ← All trials in the UK