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CompletedPhase 2

Psilocybin for Treatment-Resistant Depression

NCT05029466 · Brain and Cognition Discovery Foundation

Closed to entry
Status
Not accepting participants
Phase 2
Phase
30
Target enrolment
1
Study sites
Outside the US

What it is testing

Summary

The purpose of this study is to see if psilocybin, an investigational drug, is safe and well tolerated. Researchers also want to know if psilocybin can improve symptoms of depression. This study will see if psilocybin is safe and well tolerated by tracking changes in suicidal thoughts and behaviour, monitoring if any participants choose to stop participating in the study, and measuring any serious side effects, as well as how long they take to resolve. This study will also see if depression symptoms improve (or worsen) after psilocybin is administered. Additional information about participants' depressive symptoms and side effects will also be measured during the study.

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

  • Feasibility of the study based on participant retention

    Measured over Up to 24 weeks

  • Feasibility of the study based on suicidal ideation and behaviour scores

    Measured over Up to 24 weeks

  • Feasibility of the study based on adverse events

    Measured over Up to 24 weeks

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 to 65 Years
Ages
All
Sex
Not accepted
Healthy volunteers
Inclusion Criteria: 1. Over the age of 18 years and under the age of 65; 2. Diagnosed with major depressive disorder or bipolar II disorder by a healthcare provider; 3. Experiencing a major depressive episode (MDE) without psychotic features as defined and operationalized in the DSM-5, where the duration of the current episode is at least 3 months; 4. Have failed to respond to an adequate dose and duration of at least two guideline-concordant pharmacological treatments for the current MDE, as determined by the Massachusetts General Hospital-Antidepressant Treatment History Questionnaire; and 5. Able to complete all protocol required assessment tools without any assistance or alteration to the copyrighted assessments, and to comply with all study visits. Individuals meeting one or more of the following DSM-5-defined criteria will be excluded: * Current or past history of bipolar I disorder, schizophrenia, psychotic disorder, delusional disorder, paranoid personality disorder, or schizoaffective disorder, as assessed by a structured clinical interview (MINI) and International Personality Disorder Examination (IPDE); * First degree history of schizophrenia or any psychotic disorders, including bipolar disorder with psychotic features; * Currently experiencing symptoms of hypomania or mania as measured by the Young Mania Rating Scale (YMRS) total score \> 12; * History of a hypomanic or manic episode in the past 3 months; * History of substance use and/or alcohol use disorder, of moderate severity or greater, in the past 3 months; * Lifetime history of substance use disorder with a hallucinogen; * Lifetime history of substance-induced psychosis; * Currently experiencing psychotic symptoms as part of an MDE (mood congruent/mood incongruent). Individuals meeting one or more of the following criteria will also be excluded: * Exposure to psilocybin or any other psychedelic in the past 12 months prior to screening and/or during the current MDE; * Uncontrolled or insulin-dependent diabetes; * Seizure disorder; * Other personal circumstances or behaviour judged to be incompatible with establishment of rapport or safe exposure to psilocybin; * Women who are pregnant (self-report or via urine test), nursing, or planning a pregnancy; * Refusal to use an effective contraceptive method by the participant or participant's partner (i.e., combined estrogen- and progestogen-containing hormonal contraception or progestogen-only hormonal contraception with inhibition of ovulation; intrauterine device; intrauterine hormone-releasing system; bilateral tubal occlusion; vasectomized partner; sexual abstinence) throughout their participation in the study; * Recent stroke (\< 1 year from signing of ICF), recent myocardial infarction (\< 1 year from signing of ICF), uncontrolled hypertension (blood pressure \> 140/90 mmHg) or clinically significant arrhythmia within 1 year of signing the ICF; * Positive urine drug screen for illicit drugs or drugs of abuse at screening, a week prior to treatment, and during the trial (any positive urine drug test will be reviewed with participants to determine the pattern of use and eligibility will be determined at the investigator's discretion); * Current enrolment in any investigational drug or device study or participation in such within 30 days of screening; * Current enrolment in an interventional study for depression or participation in such within 30 days of screening; * Abnormal and clinically significant results on the physical examination, vital signs, ECG, or laboratory tests at screening; * Any other clinically significant cardiovascular, pulmonary, gastrointestinal, hepatic, renal or any other major concurrent illness that, in the opinion of the investigator, may interfere with the interpretation of the study results or constitute a health risk for the participant if he/she takes part in the study.

Where

1 study site

FacilityCityRegionCountry
Canadian Rapid Treatment Centre of Excellence (CRTCE)MississaugaOntarioCanada

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.

NCT05029466 on ClinicalTrials.gov →

Last updated in the registry 2023-07-27. Registry records change; this page reflects the data build of 2026-08-25.

Related

Where this trial sits