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

Treatment Resistant Depression

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

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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    18 and up

Participation Criteria

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

Study Location

Okanagan Clinical Trials
Okanagan Clinical Trials
Kelowna, British Columbia
Canada

Contact Study Team

Primary Contact

Emily Eisner

[email protected]
250-862-8141
Centre for Addiction and Mental Health (CAMH)
Centre for Addiction and Mental Health (CAMH)
Toronto, Ontario
Canada

Contact Study Team

Primary Contact

Alexandria Coles

[email protected]
416-535-8501
Medical Arts Health Research Centre, Kamloops
Medical Arts Health Research Centre, Kamloops
Kamloops, British Columbia
Canada

Contact Study Team

Primary Contact

Paige Dupuis, MD

[email protected]
888-736-0665
St. Michael's Hospital
St. Michael's Hospital
Toronto, Ontario
Canada

Contact Study Team

Primary Contact

Kimberly Walker

[email protected]
Medical Arts Research Group - Penticton
Medical Arts Research Group - Penticton
Penticton, British Columbia
Canada

Contact Study Team

Primary Contact

Maria Moran

[email protected]
18884904320
Diex Recherche Sherbrooke Inc.
Diex Recherche Sherbrooke Inc.
Québec, B.C.
Canada

Contact Study Team

Primary Contact

Raymond Matte, MD

[email protected]
8193462887
Chatham-Kent Clnical Trials Centre
Chatham-Kent Clnical Trials Centre
Chatham, Ontario
Canada

Contact Study Team

Primary Contact

Vanna Nguyen

[email protected]
519-397-3791
Study Sponsored By
COMPASS Pathways
Participants Required
More Information
Study ID: NCT05711940