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PET Synaptogenesis After Psilocybin In DEpression Recovery (PET-SPIDER)

Primary Purpose

Major Depressive Disorder, Anhedonia

Status
Withdrawn
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Psilocybin
Sponsored by
Washington University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Major Depressive Disorder focused on measuring Psilocybin, 11C-UCB-J, SV2A

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Men and women between 18 and 65 years of age; Able to provide informed consent Women of childbearing age must agree to be on two forms of contraception and men are required to utilize at least one form of contraception Willingness to comply and be available for all study requirements, including psychological, cognitive, and imaging for the duration of the study Meeting DSM-5 criteria for major depressive disorder and current depressive episode Snaith-Hamilton Anhedonia Pleasure Scale (SHAPS) ≥ 6 points Willing and able to taper and/or discontinue current psychotropic medications Exclusion Criteria: Women who are pregnant or who intend to become pregnant or nurse during the study duration. Presence of psychiatric conditions that are contraindications to psilocybin exposure (e.g., personal or first degree relative with history of schizophrenia spectrum or bipolar disorder); Use of psychotropic medication that may interact with psilocybin (TCA, MAOi, antipsychotic/neuroleptics, anti-epileptic/mood stabilizer, lithium, SSRI, SNRI, Mirtazapine, Buproprion, Vortioxetine). Recent use of psychedelics (psilocybin, LSD, ayahuasca, mescaline; past 5 years); or prior severe adverse reactions to psychedelics Active suicidal ideation or history of a suicide attempt. Presence of medical conditions that are contraindications to psilocybin exposure (e.g., neurological conditions or severe hypertension, severe and/or unstable metabolic or cardiovascular conditions); Current medical conditions that are known to increase risk of severe coronavirus infection or deemed by a study physician to put an individual at high risk (i.e., cancer, COPD, obesity, immunosuppression, type 2 diabetes, serious heart conditions, sickle cell disease, asthma); Presence of contraindications to PET or MRI scanning (renal disease, implantable devices, bone hardware, some IUDs); Body mass index >30 (due to MRI confounds).

Sites / Locations

  • Washington University School of Medicine

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Psilocybin

Arm Description

Eligible adults to undergo a single drug session with psilocybin (25mg tablet) plus supportive psychotherapy

Outcomes

Primary Outcome Measures

Synaptogenesis in hippocampus
Change in 11C-UCB-J signal in the hippocampus from baseline to post-treatment PET scans.
Synaptogenesis in medial prefrontal cortex
Change in 11C-UCB-J signal in the medial prefrontal cortex from baseline to post-treatment PET scans.

Secondary Outcome Measures

Change in major depressive disorder symptoms
Change in Montgomery-Asberg Depression Rating Scale (MADRS) - score range 0-60 (higher score equals greater severity of depressive symptoms).
Change in anhedonia symptoms
Change in Snaith-Hamilton Anhedonia Pleasure Scale (SHAPS) - is a 14 item self-report measure assessing pleasure response/hedonic experience across domains. The SHAPS measures both anticipation and experience of pleasure. A score is obtained by making binary (disagree/strongly disagree =1) and summing the 14 items - range 0-14, greater than 3 is considered abnormal.

Full Information

First Posted
October 17, 2022
Last Updated
January 26, 2023
Sponsor
Washington University School of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT05601648
Brief Title
PET Synaptogenesis After Psilocybin In DEpression Recovery
Acronym
PET-SPIDER
Official Title
SV2A Marker of Synaptogenesis in a Clinical Trial of Psilocybin for Depression
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Withdrawn
Why Stopped
Due to negative results in similar trials using 11C-UCB-J
Study Start Date
July 1, 2023 (Anticipated)
Primary Completion Date
January 1, 2025 (Anticipated)
Study Completion Date
July 1, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Washington University School of Medicine

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
Participants with depression will be given a single dose of psilocybin and supportive psychotherapy before, during, and after drug administration. Participants will undergo positron emission tomography (PET) imaging before and one week after psilocybin using a marker of synaptic density. This design allows us to assess the relationship between neurotrophic, and antidepressant effects produced by psilocybin.
Detailed Description
The investigators are studying the neurotrophic effects of psilocybin using 11C-UCB-J, a PET marker for synaptogenesis. Psilocybin is a naturally occurring psychedelic and exerts perceptual effects via 5-HT2A receptor agonism. Psilocybin has gained a great deal of attention as a tool for psychiatric treatment, with clinical trials demonstrating symptom relief after a single dose that is immediate and persists for months. Recognizing the therapeutic potential of psilocybin, the US Food and Drug Administration granted breakthrough therapy status to the Usona Institute for Phase 2 testing of psilocybin in depression. Animal models suggest that psychedelics exert antidepressant effects by producing a rapid and powerful neurotrophic response in the brain. The investigators will enroll patients with major depressive disorder and anhedonia. Participants will be given a single dose of psilocybin and supportive psychotherapy before, during, and after drug administration. Participants will undergo PET imaging before and one week after drug using 11C-UCB-J, a radiotracer that binds to SV2A - a marker of synaptic density and synaptogenesis. This design allows the investigators to assess the relationship between neurotrophic, and antidepressant effects produced by psilocybin.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Major Depressive Disorder, Anhedonia
Keywords
Psilocybin, 11C-UCB-J, SV2A

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Model Description
Open label treatment study, no placebo.
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Psilocybin
Arm Type
Experimental
Arm Description
Eligible adults to undergo a single drug session with psilocybin (25mg tablet) plus supportive psychotherapy
Intervention Type
Drug
Intervention Name(s)
Psilocybin
Intervention Description
Psilocybin (25mg tablet) plus supportive psychotherapy
Primary Outcome Measure Information:
Title
Synaptogenesis in hippocampus
Description
Change in 11C-UCB-J signal in the hippocampus from baseline to post-treatment PET scans.
Time Frame
7 days after psilocybin
Title
Synaptogenesis in medial prefrontal cortex
Description
Change in 11C-UCB-J signal in the medial prefrontal cortex from baseline to post-treatment PET scans.
Time Frame
7 days after psilocybin
Secondary Outcome Measure Information:
Title
Change in major depressive disorder symptoms
Description
Change in Montgomery-Asberg Depression Rating Scale (MADRS) - score range 0-60 (higher score equals greater severity of depressive symptoms).
Time Frame
7 days after psilocybin
Title
Change in anhedonia symptoms
Description
Change in Snaith-Hamilton Anhedonia Pleasure Scale (SHAPS) - is a 14 item self-report measure assessing pleasure response/hedonic experience across domains. The SHAPS measures both anticipation and experience of pleasure. A score is obtained by making binary (disagree/strongly disagree =1) and summing the 14 items - range 0-14, greater than 3 is considered abnormal.
Time Frame
7 days after psilocybin
Other Pre-specified Outcome Measures:
Title
Limbic functional connectivity, measured with resting state functional MRI
Description
Resting state functional connectivity magnetic resonance imaging measures fluctuations in blood oxygenation level dependent (BOLD) signal in the brian. Functional connectivity (FC) analysis measures correlation in BOLD signal between brain areas. FC studies of depression have suggested pathological hyperconnectivity between cortical regions involved in mood and emotion (subgenual anterior cingulate, or sgACC), and the sense of self and rumination (default mode network or DMN). Identifying correlates of neurotrophic stimulation with rsfMRI would be of tremendous value. By acquiring concurrent PET + MRI in the same subjects the investigators will directly test the viability limbic FC as a surrogate marker of synaptogenesis (measured by PET).
Time Frame
7 days after psilocybin

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men and women between 18 and 65 years of age; Able to provide informed consent Women of childbearing age must agree to be on two forms of contraception and men are required to utilize at least one form of contraception Willingness to comply and be available for all study requirements, including psychological, cognitive, and imaging for the duration of the study Meeting DSM-5 criteria for major depressive disorder and current depressive episode Snaith-Hamilton Anhedonia Pleasure Scale (SHAPS) ≥ 6 points Willing and able to taper and/or discontinue current psychotropic medications Exclusion Criteria: Women who are pregnant or who intend to become pregnant or nurse during the study duration. Presence of psychiatric conditions that are contraindications to psilocybin exposure (e.g., personal or first degree relative with history of schizophrenia spectrum or bipolar disorder); Use of psychotropic medication that may interact with psilocybin (TCA, MAOi, antipsychotic/neuroleptics, anti-epileptic/mood stabilizer, lithium, SSRI, SNRI, Mirtazapine, Buproprion, Vortioxetine). Recent use of psychedelics (psilocybin, LSD, ayahuasca, mescaline; past 5 years); or prior severe adverse reactions to psychedelics Active suicidal ideation or history of a suicide attempt. Presence of medical conditions that are contraindications to psilocybin exposure (e.g., neurological conditions or severe hypertension, severe and/or unstable metabolic or cardiovascular conditions); Current medical conditions that are known to increase risk of severe coronavirus infection or deemed by a study physician to put an individual at high risk (i.e., cancer, COPD, obesity, immunosuppression, type 2 diabetes, serious heart conditions, sickle cell disease, asthma); Presence of contraindications to PET or MRI scanning (renal disease, implantable devices, bone hardware, some IUDs); Body mass index >30 (due to MRI confounds).
Facility Information:
Facility Name
Washington University School of Medicine
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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PET Synaptogenesis After Psilocybin In DEpression Recovery

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