Clinical trial Recruiting at 1 site Phase 2 Interventional Ages 21 and up

Using psilocybin to help people quit smoking

Official title: 5-HT2A Agonist Psilocybin in the Treatment of Tobacco Use Disorder

Run by Johns Hopkins University · NCT05452772 · Data updated 2026-11-12

This study is testing if psilocybin can help daily smokers who have struggled to quit in the past to finally stop smoking, using it alongside therapy.

Quick facts

PhasePhase 2
Study typeInterventional
Ages21 Years and up
SexAll
Enrollment66 (estimated)
SponsorJohns Hopkins University
Academic / other
Locations3 sites (Birmingham, Alabama and 2 other locations)
StatusRecruiting
StartedNovember 1, 2023
Main results expectedDecember 2026
Study endsMay 2027
Registry record updatedJune 29, 2026
Trial IDNCT05452772 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults aged 21 and older who are daily smokers with a minimum of five cigarettes per day and a strong desire to quit.

Probably not a fit

Patients who do not smoke or those who have not made multiple unsuccessful attempts to quit smoking may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial investigates the efficacy of psilocybin, a 5-HT2A receptor agonist, in aiding smoking cessation among daily smokers with a history of unsuccessful quit attempts. Conducted across four experienced sites, participants will be randomly assigned to receive either psilocybin or niacin in combination with cognitive behavior therapy (CBT). The trial aims to recruit a diverse sample and will assess biologically-verified abstinence rates at various intervals. This double-blind study is designed to provide robust data on the effectiveness of psilocybin for tobacco use disorder.

Why it matters

Potential benefit: If successful, this treatment could significantly improve smoking cessation rates for individuals struggling with tobacco use disorder.

How similar studies have gone: Previous studies have shown promising results for psilocybin in smoking cessation, but this double-blind approach is novel and has not been extensively tested.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* 21 years old or older
* Be a daily smoker (minimum of 5 cigarettes/day on a typical day and breath CO of 6 or greater at screening) with multiple unsuccessful previous quit attempts, and report a continued desire to quit smoking
* Read, write, and speak English
* Agree to abstain from smoking for the psilocybin/niacin session from 1 hour before psilocybin/niacin administration until at least 8 hours afterward
* Agree to refrain from using any psychoactive drugs, including alcoholic beverages, within 24 hours of psilocybin/niacin administration
* Be healthy as determined by screening for medical problems via a personal interview, a medical questionnaire, a physical examination, an electrocardiogram (ECG), and routine medical blood and urinalysis lab tests. See Exclusion Criteria below for specific ECG and specific blood test criteria

Exclusion Criteria:

* The use of e-cigarettes or tobacco products other than machine-manufactured combustible cigarettes (e.g., cigarillos) on more than 5 of the previous 30 days
* Women who are pregnant (positive pregnancy test) or nursing, or are not practicing an effective means of birth control
* Positive urine drug screen for illicit drugs (excluding cannabis)
* Positive urine breath test for alcohol. Participants with positive tests will be rescheduled
* For blood samples, the following lab values will be exclusionary: transaminases greater than x2 the upper limit of normal lab reference range, hemoglobin less than 11 g/d, and creatinine clearance \< 40 ml/min using the Cockroft-Gault equation.
* For ECG screening: The ECG will be read by a cardiologist. Corrected heart rate (QTc) greater than 450 msec will be excluded.
* Patients who have baseline vital signs that exceed the following measurements will be excluded from participation: Systolic blood pressure (SBP) \> 139 mmHG, diastolic blood pressure (DBP)\> 89 mmHG, and heart rate of \<=95 beats per minute (BPM). The investigators will perform serial heart rate monitoring with 3 total attempts. That is, heart rate must be \<=95 bpm on one of these attempts to be included in the study.
* Currently taking on a regular basis (e.g., daily) antidepressants of any drug class, antipsychotics, or monoamine oxidase inhibitors (MAOIs), or serotonin-acting dietary supplements (e.g., 5-hydroxy- tryptophan, St. John's wort). Currently taking efavirenz, Acetaldehyde dehydrogenase inhibitors such as disulfiram (Antabuse), Alcohol dehydrogenase inhibitors, or uridine diphosphate glucuronosyltransferase 1-9 (UGT1A9) inhibitors or uridine diphosphate glucuronosyltransferase 1-10 (UGT1A10) inhibitors such as phenytoin, regorafenib, eltrombopag. For individuals who have intermittent or "as needed" use of such medications, psilocybin sessions will not be conducted until at least 5 half-lives of the agent have elapsed after the last dose
* Current use of medications for smoking cessation (i.e., varenicline, nicotine replacement products, bupropion)
* Current neurological illnesses including, but not limited to, seizure disorders, frequent migraines or on prophylaxis, multiple sclerosis, movement disorders, history of significant head trauma (loss of consciousness \> 24 hours), or central nervous system (CNS) tumor
* Recent (within the past 12 months) or an extensive history of psychedelic use (\>20 lifetime uses)
* Current or past history of meeting Diagnostic and Statistical Manual of Mental Disorders (DSM-5) criteria for Schizophrenia, Psychotic Disorder (unless substance-induced or due to a medical condition), or Bipolar I or II Disorder. Current or past history within the last 5 years of meeting DSM-5 criteria for alcohol or drug use disorder (excluding caffeine and nicotine) or severe major depression
* Recent (past year) history of suicidal behavior or attempt or high-level current suicidal ideation assessed by the Columbia Suicide Severity Rating Scale (C-SSRS)
* Have a first- or second-degree relative with schizophrenia, psychotic disorder (unless substance induced or due to a medical condition), or bipolar I or II disorder
* Currently meets DSM-5 criteria for Dissociative Disorder, Anorexia Nervosa, Bulimia Nervosa, Major Depression, or Post-traumatic Stress Disorder

Where it's running

  • University of Alabama at Birmingham
    Birmingham, Alabama, United States
    Recruiting
  • Johns Hopkins University School of Medicine
    Baltimore, Maryland, United States
    Active not recruiting
  • New York University
    New York, New York, United States
    Active not recruiting

Study contacts

  • Principal investigator: Matthew Johnson, Ph.D — Johns Hopkins University
  • Study coordinator: Matthew Johnson, Ph.D
  • Email: mwj@jhu.edu
  • Phone: 410-550-0056

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

  • Personalized brain-targeted TMS for smoking cessation

    A personalized brain-guided Transcranial Magnetic Stimulation (TMS) approach is tested against a standard TMS method to see if it better changes reward brain activity and reduces cravings and smoking in adults with tobacco use disorder.

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  • TUBSIS 2.0 — an online program to help adults reduce or quit smoking and vaping

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  • Impact of Menthol vs. Non-Menthol Cigarettes on Abuse Liability

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  • Facilitating Tobacco Treatment in Veterans with Serious Mental Illness

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.