The Safety and Efficacy Of Psilocybin as an Adjunctive Therapy in Participants With Treatment Resistant Depression
Primary Purpose
Treatment Resistant Depression
Status
Completed
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
Psilocybin
Sponsored by
About this trial
This is an interventional treatment trial for Treatment Resistant Depression
Eligibility Criteria
Inclusion Criteria:
- Signed ICF.
- 18 years of age or older
- At least moderate MDD
- Hamilton Depression Rating Scale (17 item) score ≥18
- Currently receiving treatment with a selective serotonin reuptake inhibitor
- Failure to respond to an adequate dose and duration of 2, 3, or 4 pharmacological treatments
- McLean Screening Instrument for Borderline Personality Disorder <7 at Screening (V1).
- Ability to complete all protocol required assessment tools without any assistance or alteration to the copyrighted assessments, and to comply with all study visits.
Exclusion Criteria:
Psychiatric Exclusion Criteria:
- Current or past history of schizophrenia, psychotic disorder (unless substance induced or due to a medical condition), bipolar disorder, delusional disorder, paranoid personality disorder, schizoaffective disorder, or borderline personality disorder, as assessed by medical history, McLean Screening Instrument for Borderline Personality Disorder and a structured clinical interview (version 7.0.2 MINI).
- Prior electroconvulsive therapy and/or ketamine for current episode.
- Ongoing use of an antidepressant medication, including augmentation or combination therapies, other than a single SSRI
- Current psychological therapies that will not remain stable within 21 days of the psilocybin session. Psychological therapies cannot be initiated within 21 days of baseline.
- Current (within the last year) alcohol or substance use disorder as informed by DSM 5 (diagnosed by MINI 7.0.2) at Screening (V1).
- Significant suicide risk as defined C-SSRS within the past year
- Depression secondary to other severe medical conditions according to clinicians' judgement.
Other personal circumstances and behaviour judged to be incompatible with establishment of rapport or safe exposure to psilocybin, including exposure to psilocybin within the past year and use of psychedelics, such as ayahuasca, during the current depressive episode.
General Medical Exclusion Criteria:
- Women who are pregnant, nursing or planning a pregnancy.
- Cardiovascular conditions
- Uncontrolled or insulin dependent diabetes.
- Seizure disorder.
- Positive urine drug screen for illicit drugs or drugs of abuse
- Current enrolment in any investigational drug or device study or participation in such within 30 days prior to Screening (V1).
- Current enrolment in another clinical study of an investigational medical or participation in such within 30 days of Screening (V1).
- Abnormal and clinically significant results on the physical examination, vital signs, ECG or laboratory tests at Screening (V1).
- 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.
Sites / Locations
- Kadima Neuropsychiatry Institute
- Sheaf House, Tallaght Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Psilocybin
Arm Description
25mg Psilocybin
Outcomes
Primary Outcome Measures
Improvement in depressive symptoms
Change in Montgomery-Asberg Depression Rating Scale total score from Baseline to 3 weeks post psilocybin administration.
The minimum and maximum values are 0 and 6 and a higher score means a worse outcome.
Secondary Outcome Measures
Incidence of response
The proportion of participants with a response (defined as a ≥ 50% improvement in Montgomery-Asberg Depression Rating Scale total score from Baseline) at Week 3 post psilocybin administration.
The minimum and maximum values are 0 and 60 and a higher score means a worse outcome.
Incidence of remission
The proportion of participants with remission (defined as Montgomery-Asberg Depression Rating Scale total score ≤ 10) at Week 3 post psilocybin administration The minimum and maximum values are 0 and 60 and a higher score means a worse outcome.
Improvement in Clinical Global Impression - Severity
Changes from Baseline in Clinical Global Impression-Severity score at Week 3 post psilocybin administration.
The minimum and maximum values are 1 and 7 and a higher score means a worse outcome.
The minimum and maximum values are 0 and 7, respectively and a higher scores means a worse outcome.
Adverse Events
Incidence of Adverse Events
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04739865
Brief Title
The Safety and Efficacy Of Psilocybin as an Adjunctive Therapy in Participants With Treatment Resistant Depression
Official Title
The Safety and Efficacy Of Psilocybin as an Adjunctive Therapy in Participants With Treatment Resistant Depression
Study Type
Interventional
2. Study Status
Record Verification Date
September 2021
Overall Recruitment Status
Completed
Study Start Date
September 15, 2020 (Actual)
Primary Completion Date
October 14, 2021 (Actual)
Study Completion Date
October 14, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
COMPASS Pathways
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
A recent open label study of the effects of psilocybin in participants with treatment-resistant depression (TRD) showed rapid significant decrease of depressive symptoms after treatment with psilocybin coupled with psychological support. Over 40% of participants sustained response at 3 months. In this study, the aim is to explore effectiveness of 25 mg of psilocybin as an adjunctive therapy in participants with TRD.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Treatment Resistant Depression
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Model Description
Open label
Masking
None (Open Label)
Allocation
N/A
Enrollment
19 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Psilocybin
Arm Type
Experimental
Arm Description
25mg Psilocybin
Intervention Type
Drug
Intervention Name(s)
Psilocybin
Other Intervention Name(s)
COMP360
Intervention Description
Open label
Primary Outcome Measure Information:
Title
Improvement in depressive symptoms
Description
Change in Montgomery-Asberg Depression Rating Scale total score from Baseline to 3 weeks post psilocybin administration.
The minimum and maximum values are 0 and 6 and a higher score means a worse outcome.
Time Frame
3 weeks
Secondary Outcome Measure Information:
Title
Incidence of response
Description
The proportion of participants with a response (defined as a ≥ 50% improvement in Montgomery-Asberg Depression Rating Scale total score from Baseline) at Week 3 post psilocybin administration.
The minimum and maximum values are 0 and 60 and a higher score means a worse outcome.
Time Frame
3 weeks
Title
Incidence of remission
Description
The proportion of participants with remission (defined as Montgomery-Asberg Depression Rating Scale total score ≤ 10) at Week 3 post psilocybin administration The minimum and maximum values are 0 and 60 and a higher score means a worse outcome.
Time Frame
3 weeks
Title
Improvement in Clinical Global Impression - Severity
Description
Changes from Baseline in Clinical Global Impression-Severity score at Week 3 post psilocybin administration.
The minimum and maximum values are 1 and 7 and a higher score means a worse outcome.
The minimum and maximum values are 0 and 7, respectively and a higher scores means a worse outcome.
Time Frame
3 weeks
Title
Adverse Events
Description
Incidence of Adverse Events
Time Frame
3 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Signed ICF.
18 years of age or older
At least moderate MDD
Hamilton Depression Rating Scale (17 item) score ≥18
Currently receiving treatment with a selective serotonin reuptake inhibitor
Failure to respond to an adequate dose and duration of 2, 3, or 4 pharmacological treatments
McLean Screening Instrument for Borderline Personality Disorder <7 at Screening (V1).
Ability to complete all protocol required assessment tools without any assistance or alteration to the copyrighted assessments, and to comply with all study visits.
Exclusion Criteria:
Psychiatric Exclusion Criteria:
Current or past history of schizophrenia, psychotic disorder (unless substance induced or due to a medical condition), bipolar disorder, delusional disorder, paranoid personality disorder, schizoaffective disorder, or borderline personality disorder, as assessed by medical history, McLean Screening Instrument for Borderline Personality Disorder and a structured clinical interview (version 7.0.2 MINI).
Prior electroconvulsive therapy and/or ketamine for current episode.
Ongoing use of an antidepressant medication, including augmentation or combination therapies, other than a single SSRI
Current psychological therapies that will not remain stable within 21 days of the psilocybin session. Psychological therapies cannot be initiated within 21 days of baseline.
Current (within the last year) alcohol or substance use disorder as informed by DSM 5 (diagnosed by MINI 7.0.2) at Screening (V1).
Significant suicide risk as defined C-SSRS within the past year
Depression secondary to other severe medical conditions according to clinicians' judgement.
Other personal circumstances and behaviour judged to be incompatible with establishment of rapport or safe exposure to psilocybin, including exposure to psilocybin within the past year and use of psychedelics, such as ayahuasca, during the current depressive episode.
General Medical Exclusion Criteria:
Women who are pregnant, nursing or planning a pregnancy.
Cardiovascular conditions
Uncontrolled or insulin dependent diabetes.
Seizure disorder.
Positive urine drug screen for illicit drugs or drugs of abuse
Current enrolment in any investigational drug or device study or participation in such within 30 days prior to Screening (V1).
Current enrolment in another clinical study of an investigational medical or participation in such within 30 days of Screening (V1).
Abnormal and clinically significant results on the physical examination, vital signs, ECG or laboratory tests at Screening (V1).
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Guy Goodwin
Organizational Affiliation
University of Oxford
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kadima Neuropsychiatry Institute
City
La Jolla
State/Province
California
ZIP/Postal Code
92037
Country
United States
Facility Name
Sheaf House, Tallaght Hospital
City
Dublin
Country
Ireland
12. IPD Sharing Statement
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The Safety and Efficacy Of Psilocybin as an Adjunctive Therapy in Participants With Treatment Resistant Depression
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