Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at UCSD
Dates
study started
study ends around
Principal Investigator
by Cory Weissman, MD (ucsd)

Description

Summary

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

Official Title

A Phase III, Multicentre, Randomised, Double-blind, Controlled Study to Investigate the Efficacy, Safety, and Tolerability of Two Administrations of COMP360 in Participants With Treatment-resistant Depression

Details

This is a phase III, international, multi-centre, randomised, parallel group, fixed repeat dose, double-blind, controlled study. The study population will include participants aged ≥18 years with TRD.

Overall, 568 participants are to be randomised in a 2:1:1 ratio to receive COMP360 25 mg, 10 mg or 1 mg.

The study comprises three parts (A, B, and C) and will last approximately 62 weeks including a three- to ten-week screening period.

Part A will include a nine-week follow-up from initial investigational product (IP) administration.

Part B will include a further 17 weeks follow-up out to 26 weeks from initial IP administration.

Part C will include a further 26 weeks follow-up out to 52 weeks from initial IP administration.

In this study, the aim is to assess the efficacy of COMP360, administered with psychological support in adult participants with TRD, in improving symptoms of depression.

Keywords

Treatment Resistant Depression, psilocybin, Treatment-Resistant Depressive Disorder

Eligibility

You can join if…

Open to people ages 18 years and up

  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

You CAN'T join if...

  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

Locations

  • The Regents of the University of California - San Diego accepting new patients
    La Jolla 5363943 California 5332921 92037-1337 United States
  • CalNeuro Research Group, Inc accepting new patients
    Los Angeles 5368361 California 5332921 90025 United States
  • Kadima Neuropsychiatry Institute accepting new patients
    La Jolla 5363943 California 5332921 92037 United States
  • M3 Wake Research accepting new patients
    Encino 5346649 California 5332921 91316 United States
  • Syrentis Clinical Research accepting new patients
    Santa Ana 5392900 California 5332921 92705 United States
  • ATP Clinical Research, Inc. accepting new patients
    Orange 5379513 California 5332921 92868 United States
  • Piedmont Hospital Neuroscience Centre accepting new patients
    Oakland 5378538 California 5332921 94610 United States
  • Clinical Innovations, Inc. accepting new patients
    Bellflower 5327422 California 5332921 90706 United States
  • Stanford University accepting new patients
    Stanford 5398563 California 5332921 94305 United States

Lead Scientist at University of California Health

  • Cory Weissman, MD (ucsd)
    Associate Professor Of Clinical, Psychiatry, Vc-health Sciences-schools. Authored (or co-authored) 33 research publications

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
COMPASS Pathways
ID
NCT05711940
Phase
Phase 3 research study
Study Type
Interventional
Participants
Expecting 568 study participants
Last Updated