Psilocybin for Treatment-Resistant Depression

• ClinicalTrials.gov Identifier: NCT05029466
• Recruitment Status: Completed
• First Posted: August 31, 2021
• Last Update Posted: July 27, 2023
• Sponsor: Brain and Cognition Discovery Foundation
• Collaborators: Braxia Scientific Corp.; Usona Institute
• Information provided by (Responsible Party): Brain and Cognition Discovery Foundation

Tracking Information

• First Submitted Date: August 20, 2021
• First Posted Date: August 31, 2021
• Last Update Posted Date: July 27, 2023
• Actual Study Start Date: November 19, 2021
• Actual Primary Completion Date: July 22, 2023 (Final data collection date for primary outcome measure)

Current Primary Outcome Measures (submitted: August 26, 2021)

• Feasibility of the study based on participant retention [ Time Frame: Up to 24 weeks ]
  Participant drop-out rates will be calculated to determine the feasibility of psilocybin in adults with treatment-resistant depression.
• Feasibility of the study based on suicidal ideation and behaviour scores [ Time Frame: Up to 24 weeks ]
  Feasibility will be judged based on change in Columbia Suicide Severity Rating Scale (CSSRS) scores. The CSSRS evaluates suicidal ideation and behaviour. The suicidal ideation score ranges from 0 (no ideation) to 5 (active suicidal ideation with specific plan and intent). Suicidal ideation intensity score ranges from 0 (no ideation) to 25 (most severe). The presence of suicidal behaviour is rated as a binary response; the lethality of actual attempts are rated on a scale of 0 (no or very minor physical damage) to 5 (death) and the potential lethality of actual attempts are rated on a scale of 0 (behaviour not likely to result in injury) to 2 (behaviour likely to result in death despite available medical care).
• Feasibility of the study based on adverse events [ Time Frame: Up to 24 weeks ]
  Feasibility will be judged based on the percentage of participants experiencing serious adverse events and the percentage of adverse events resolving within 48 hours of each dose administration.

• Original Primary Outcome Measures: Same as current

Current Secondary Outcome Measures (submitted: August 26, 2021)

• Montgomery-Åsberg Depression Rating Scale (MADRS) total score [ Time Frame: Up to 24 weeks ]
  The MADRS is a clinician-rated scale measuring depression severity, consisting of 10 items, each scored from 0 (normal) to 6 (severe), for a total possible score of 60; higher scores denote greater severity.
• Montgomery-Åsberg Depression Rating Scale (MADRS) response rate [ Time Frame: Up to 24 weeks ]
  The proportion of participants with at least a 50% reduction in MADRS total score relative to baseline.
• Montgomery-Åsberg Depression Rating Scale (MADRS) remission rate [ Time Frame: Up to 24 weeks ]
  The proportion of participants with a MADRS total score of 10 or lower.
• McIntyre and Rosenblat Rapid Response Scale (MARRRS) [ Time Frame: Up to 24 weeks ]
  The MARRS was recently validated in adults with treatment-resistant major depressive or bipolar disorder receiving open-label intravenous ketamine at a community-based treatment center The MARRRS is a self-reported 14-item self-report measure of depressive symptoms present during the past 72 hours. Total score ranges from 0 to 42; a higher score indicates greater symptom severity.
• Patient Health Questionnaire 9-item (PHQ-9) [ Time Frame: Up to 24 weeks ]
  The PHQ-9 is a self-rated measure of depressive symptom severity in the past two weeks. Each of the nine items is rated on a Likert scale, ranging from 0 (not at all) to 3 (nearly every day), and summed for a total score between 0 (no symptoms) to 27 (most severe).
• Clinical Global Impressions Scale (CGI) [ Time Frame: Up to 24 weeks ]
  The CGI severity module assesses the severity of a person's depressive illness using a seven-point Likert scale, ranging from "Normal, not at all depressed" to "Among the most extremely depressed patients". The CGI improvement module evaluates the global improvement of a person's condition since their last visit on a seven-point Likert scale, ranging from "Very much improved" to "Very much worse".
• Quick Inventory for Depressive Symptomatology, Self-Report, 16-item (QIDS-SR-16) [ Time Frame: Up to 24 weeks ]
  The QIDS-SR-16 total score ranges from 0 to 27 with 0 representing no depression and 27 representing severe depression.
• Columbia Suicide Severity Rating Scale (CSSRS) [ Time Frame: Up to 24 weeks ]
  The CSSRS evaluates suicidal ideation and behaviour. The suicidal ideation score ranges from 0 (no ideation) to 5 (active suicidal ideation with specific plan and intent). Suicidal ideation intensity score ranges from 0 (no ideation) to 25 (most severe). The presence of suicidal behaviour is rated as a binary response; the lethality of actual attempts are rated on a scale of 0 (no or very minor physical damage) to 5 (death) and the potential lethality of actual attempts are rated on a scale of 0 (behaviour not likely to result in injury) to 2 (behaviour likely to result in death despite available medical care).
• Clinician-Administered Dissociative States Scale (CADSS), 23-item [ Time Frame: Up to 20 weeks ]
  Total scores on the 23-item CADSS range from 0 to 92; a higher score denotes greater dissociative symptom severity.
• Clinician-Administered Dissociative States Scale (CADSS), 6-item [ Time Frame: Up to 20 weeks ]
  Total scores on the 6-item CADSS range from 0 to 24; a score of 3 or greater denotes the presence of dissociation symptom severity.
• Brief Psychiatric Rating Scale (BPRS) [ Time Frame: Up to 20 weeks ]
  The BPRS rating scale has 18 items, each item rated on a severity scale of 1 (not present) to 7 (extremely severe). 0 is entered if the item is not assessed.
• Young Mania Rating Scale (YMRS) [ Time Frame: Up to 20 weeks ]
  Total scores range from 0 to 60, with higher scores indicative of greater symptom severity.
• Mystical Experiences Questionnaire (MEQ) [ Time Frame: Up to 20 weeks ]
  The MEQ consists of 30 items, each item rated on a Likert scale (0-None/not at all to 5-Extreme, more than any other time in my life). The MEQ total score is computed by taking the average response to all items.
• Sheehan Disability Scale (SDS) [ Time Frame: Up to 24 weeks ]
  The SDS total score ranges from 0 to 30 with 0 representing no impairment and 30 representing severe impairment. The last two items of the scale (Days Lost and Days Unproductive) range from 0 to 7 (higher number denotes greater impairment).
• EuroQol-5D 5-Level (EQ-5D-5L) [ Time Frame: Up to 24 weeks ]
  The EQ-5D-5L consists of 5 items; each item ranges from 1 (no problems) to 5 (extreme problems). A participant's self-rated health is recorded on a vertical visual analogue scale (range 100 to 0), where the endpoints are labelled 'The best health you can imagine' (100) and 'The worst health you can imagine' (0).
• World Health Organization-5 Well-Being Index (WHO-5) [ Time Frame: Up to 24 weeks ]
  The WHO-5 is a measure of overall well-being, rated on a scale of 0 to 25, with higher scores denoting higher quality of life.
• World Productivity and Impairment Questionnaire (WPAI) [ Time Frame: Up to 24 weeks ]
  The WPAI is a six-item self-administered rating scale measuring work absenteeism, presenteeism, and productivity loss and daily activity impairment. Individuals are asked to rate to what extent health problems affected their ability to do regular daily activities other than work at a job (0-No effect on daily activities to 10-Completely prevented me from doing my daily activities). Respondents who are currently employed are additionally asked to rate the number of hours missed from work due to health problems, the number of hours missed due to other reasons (e.g., vacation, time off to participate in this study), and the number of hours worked in the past seven days, as well as to what extent health problems affected productivity while working (0-No effect on my work to 10-Completely prevented me from working). Responses to each question are scaled to an overall percentage score (0 to 100), with higher values denoting greater impairment
• Perceived Deficits Questionnaire - Depression - 5-Item (PDQ-5-D) [ Time Frame: Up to 24 weeks ]
  The total score ranges from 0 to 20, with greater scores indicative of greater subjective cognitive impairment.
• Digit Symbol Substitution Test (DSST) [ Time Frame: Up to 24 weeks ]
  The DSST assesses relative contributions of speed, memory, executive function and visual scanning. Participants are required to copy symbols that are paired with simple geometric shapes or numbers within 90 seconds for a total possible score of 0 to 90. A higher score reflects greater performance.
• Trail Making Test A (TMT-A) [ Time Frame: Up to 24 weeks ]
  The TMT is a two-part cognitive test. TMT-A assesses cognitive processing speed and consists of 25 circles distributed over a sheet of paper. Participants are asked to connect circles in numerical sequence. If a participant makes a mistake, the administrator points out the error, and the participant must return to the last correct circle and continue the task. Lower scores represent better performance.
• Trail Making Test B (TMT-B) [ Time Frame: Up to 24 weeks ]
  The TMT is a two-part cognitive test. TMT-B assesses executive functioning and consists of 25 circles distributed over a sheet of paper. Participants are asked to connect circles in alternating numerical and alphabetical sequence (e.g., 1-A-2-B). If a participant makes a mistake, the administrator points out the error, and the participant must return to the last correct circle and continue the task. Lower scores represent better performance.
• Generalized Anxiety Disorder-7 (GAD-7) [ Time Frame: Up to 24 weeks ]
  Total score ranges from 0 to 21; a higher score denotes greater symptom severity.
• Snaith-Hamilton Pleasure Scale (SHAPS) [ Time Frame: Up to 24 weeks ]
  The SHAPS total score ranges from 14 to 56, wherein a higher score indicates greater hedonic capacity (lower anhedonic severity).
• Peripheral inflammatory and metabolic biomarkers [ Time Frame: Up to 2 weeks ]
  Inflammatory, neuroplasticity, and metabolic targets that are hypothesized to be relevant to the therpeutic mechanism of psilocybin in depression (e.g., interleukin-6, brain-derived neurotrophic factor, insulin, leptin).

• Original Secondary Outcome Measures: Same as current
• Current Other Pre-specified Outcome Measures: Not Provided
• Original Other Pre-specified Outcome Measures: Not Provided

Descriptive Information

• Brief Title: Psilocybin for Treatment-Resistant Depression
• Official Title: The Efficacy and Tolerability of Psilocybin in Participants With Treatment-Resistant Depression: a Phase 2, Randomized Feasibility Study
• Brief 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.
• Detailed Description: This randomized clinical trial will assess the feasibility, safety, and efficacy of single and repeat doses of psilocybin at point-of-care in persons with treatment-resistant depression as part of major depressive disorder or bipolar II disorder. The primary objective is to evaluate the feasibility of psilocybin in adults with treatment-resistant depression. The secondary objectives are to assess the efficacy and tolerability of psilocybin at point-of-care.
• Study Type: Interventional
• Study Phase: Phase 2
• Study Design: Allocation: Randomized; Intervention Model: Parallel Assignment; Masking: None (Open Label); Primary Purpose: Treatment
• Condition: Treatment Resistant Depression

Intervention

Drug: Psilocybin

Participants will receive a single dose of psilocybin and be assessed weekly for six weeks and biweekly for 18 weeks. Participants who relapse may receive up to two repeated doses of psilocybin.

Study Arms

• Experimental: Immediate treatment
  Participants will commence psilocybin treatment immediately upon study enrollment.
  Intervention: Drug: Psilocybin
• Experimental: Delayed treatment
  Participants will commence psilocybin treatment two weeks after study enrollment.
  Intervention: Drug: Psilocybin

• Publications *: Not Provided

Recruitment Information

• Recruitment Status: Completed
• Actual Enrollment (submitted: August 26, 2021): 30
• Original Estimated Enrollment: Same as current
• Actual Study Completion Date: July 22, 2023
• Actual Primary Completion Date: July 22, 2023 (Final data collection date for primary outcome measure)

Eligibility Criteria

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.

Sex/Gender

• Sexes Eligible for Study: All

• Ages: 18 Years to 65 Years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Contacts: Contact information is only displayed when the study is recruiting subjects
• Listed Location Countries: Canada

Administrative Information

• NCT Number: NCT05029466
• Other Study ID Numbers: 253490
• Has Data Monitoring Committee: Not Provided

U.S. FDA-regulated Product

• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No

IPD Sharing Statement

• Plan to Share IPD: No

• Current Responsible Party: Brain and Cognition Discovery Foundation
• Original Responsible Party: Same as current
• Current Study Sponsor: Brain and Cognition Discovery Foundation
• Original Study Sponsor: Same as current

Collaborators

• Braxia Scientific Corp.
• Usona Institute

Investigators

• Principal Investigator: Joshua D Rosenblat, MD, MSc; Canadian Rapid Treatment Centre of Excellence

• PRS Account: Brain and Cognition Discovery Foundation
• Verification Date: July 2023