Not Yet RecruitingPhase 2psilocybin

Psilocybin Therapy for Methamphetamine Use Disorder and HIV

Sponsored by Nicky Mehtani, MD, MPH

NCT ID
NCT07756736
Target Enrollment
30 participants
Start Date
2026-11
Est. Completion
2029-06

About This Study

The goal of this clinical trial is to learn whether it is possible to use psilocybin in combination with motivational support therapy to treat moderate-to-severe methamphetamine use disorder (MeUD) in people with HIV who are seeking to stop using methamphetamine. The main questions it aims to answer are: * Do people with HIV and MeUD find psilocybin with motivational support therapy feasible and acceptable as a potential treatment? * Is psilocybin safe and tolerable among people with HIV and MeUD? Participants will: * Be randomly assigned to receive a single monitored dose of either 25 mg (higher dose) or 5 mg (lower dose) psilocybin * Have 3 preparation and 3 integration motivational support therapy visits before and after the psilocybin dosing session. * Report their methamphetamine use prior to, during, and up to 3 months following the intervention * Optionally receive one additional open-label 25 mg psilocybin session after the 4-week assessment, if eligible

Conditions Studied

Methamphetamine Use DisorderHuman Immunodeficiency Virus (HIV)

Interventions

  • Psilocybin 5 mg
  • Psilocybin 25 mg
  • Motivational Support

Eligibility

Age:25 Years - 64 Years
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* Age 25 to 64
* Diagnosed with HIV at least 3 months ago
* Moderate-to-severe methamphetamine use disorder
* Uses methamphetamine regularly and identifies it as their primary drug
* Has a goal of quitting methamphetamine use
* Able and willing to abstain from methamphetamine and other non-prescribed drugs for at least 24 hours prior to and throughout psilocybin dosing sessions
* Currently living indoors with stable housing anticipated for the duration of the study
* Has a text-capable cellphone
* Willing to use highly effective contraception and not donate sperm throughout the study
* Able to participate in study procedures in English

Exclusion Criteria:

* History of any primary psychotic disorder (e.g., schizophrenia or schizoaffective disorder), bipolar I disorder, or certain other psychiatric conditions as determined by study assessment
* Current moderate-to-severe opioid, alcohol, or sedative use disorder (Note: people on stable doses of buprenorphine or methadone may be eligible)
* Currently taking certain medications that may interact with psilocybin
* Recent use of a psychedelic drug
* Certain significant heart, liver, or kidney conditions
* Uncontrolled high blood presure (i.e., \>150/90 mmHg)
* History of stroke or seizure in the past year
* Current pregnancy or breastfeeding
* Current involvement in the criminal legal system that would be expected to interfere with study participation
* Current or planned enrollment in a contingency management program or another investigational substance use treatment trial within the past month

Note: Additional eligibility criteria apply. Certain criteria and thresholds are not listed here to preserve the scientific integrity of the study.

Study Locations (1)

UCSF at Zuckerberg San Francisco General Hospital
San Francisco, California, United States

Interested in this trial?

Contact the study team to learn more about eligibility and enrollment.

Eliza Banbury, BA
CONTACT
510-985-3522prism.trial@ucsf.edu
View on ClinicalTrials.gov
Data Source
ClinicalTrials.gov

Last updated from source