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RecruitingPhase 2

Psilocybin With Pimavanserin Compared to Psilocybin Alone for the Treatment of Major Depressive Disorder

NCT06592833 · Icahn School of Medicine at Mount Sinai

Recruiting
Status
Accepting participants
Phase 2
Phase
60
Target enrolment
1
Study sites
1 US states

What it is testing

Summary

This is an interventional, parallel arm assignment treatment study in individuals with Major Depressive Disorder (MDD). Each individual will be treated with a single dose of pimavanserin or placebo plus a single dose of psilocybin. Evaluations will be taken before dosing and following dosing at several timepoints up to 5 weeks post-dosing.

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

  • Mystical Experience Questionnaire (MEQ-30) Score

    Measured over 6 hours post-treatment

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

21 Years to 80 Years
Ages
All
Sex
Not accepted
Healthy volunteers
Inclusion Criteria: * Age 21-80 years, any gender * Current primary diagnosis of Unipolar Major Depressive Disorder (MDD) without psychotic features using DSM-5 criteria * 24-item Hamilton Rating Scale for Depression (HRSD) ≥16 * Current diagnosis of Major Depressive Episode (MDE) * Capable of providing informed consent and complying with study procedures * Currently using or agreeing to use a highly effective contraception, if person of childbearing potential (such as condoms, IUD, or oral contraceptive), for duration of the study. Male participants agree to use highly effective contraception with partners of childbearing potential * Discontinuation of any serotonergic drug for at least 2 weeks or 5 half-lives (whichever of the two is longer) prior to psilocybin exposure Exclusion Criteria: * Any severity of substance use disorder in the last 6 months (excluding tobacco use disorder) as determined by DSM-V criteria via the SCID * Current psychiatric hospitalization or psychiatric hospitalization within the last 6 months * Use of psychedelics in the last 12 months * Non-medical or illicit use of ketamine in the past 12 months * Negative reaction after prior use of psychedelics * Past or current psychotic disorder (including psychotic MDD), mania, or bipolar disorder * Severe depression as indicated by Clinical Global Impressions (CGI)-Severity score ≥ 5 at baseline * Significant suicidal ideation as indicated by C-SSRS \> 2 in the past 6 months at time of screening * Suicide attempt in the past 2 years, or clinician concern that the patient poses a risk to self or others * Acute, severe, or unstable medical illness * Weight \> 300 lbs., or girth size incompatible with scanner bore * Any conditions/qualities that make participation in MRI imaging unsafe\* * Any physical or intellectual disability adversely affecting ability to complete assessments. * Current pregnancy or currently breast feeding. * Any clinically significant abnormal lab test result, including clinically significant abnormal baseline liver and/or renal function tests * Currently being treated with a contraindicated medication. Contraindicated medications include antipsychotic medications, serotonergic antidepressant medications, and mood stabilizers that may attenuate the effects of psilocybin. Strong CYP3A4 inhibitors and inducers are also contraindicated. UGT1A9 and UGT1A10 inhibitors, monoamine oxidase, and aldehyde or alcohol dehydrogenase inhibitors are prohibited concomitant medications. * History of abnormal QT prolongation or QTc interval \>450 ms on screening * Use of medications known to prolong the QT interval * Any congenital prolongation of the QT interval or a family history of long QT syndrome * A family history of sudden cardiac or unexplained death * A family history in a first-degree relative of psychosis/schizophrenia or related disorders * A first-degree family history of bipolar disorder * A history of cardiac arrhythmias or who require treatment with an antiarrhythmic medication * A history of any cardiovascular disorder/condition known to increase the possibility of QT prolongation, or any other risk factors for prolonged QT interval/tosades de pointes (including symptomatic bradycardia, hypokalemia, hypomagnesemia, hypocalcemia, heart failure, or Brugada Syndrome) * Preexisting cardiovascular conditions, including cardiac valvulopathy, pulmonary hypertension, hypertension, tachycardia, and any cardiovascular conditions that may be worsened/exacerbated by elevated blood pressure or heart rate. * Baseline vital sign parameters at screening and on day of dosing prior to dose that exceed to the following values for systolic blood pressure (SBP), diastolic (DBP), and heart rate (HR): SBP \> 139 mmHg, DBP 89 mmHg, and HR \> 90 bpm * Hypersensitivity to either psilocybin or pimavanserin * Psychiatric or other condition judged to be incompatible with establishment of rapport with therapy team and/or safe exposure to psilocybin * Positive urine toxicology at screening * Any clinically significant abnormalities on 12-lead electrocardiogram (ECG) * Mini-Mental State Examination (MMSE) score \< 25 * Brief Psychiatric Rating Scale (BPRS-6) \> 5 * Potential fall risk

Where

1 study site

FacilityCityRegionCountry
Icahn School of Medicine at Mount Sinai, Center for Psychedelic Therapy ResearchNew YorkNew YorkUnited States

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.

NCT06592833 on ClinicalTrials.gov →

Last updated in the registry 2025-05-14. Registry records change; this page reflects the data build of 2026-08-25.

Related

Where this trial sits