Alcohol Use DisorderPhase 2NCT07296094
Psilocybin-Assisted Psychotherapy for the Treatment of Severe Alcohol Use Disorder
A Phase 2 study testing Psilocybin in people with Alcohol Use Disorder, run by Brigham and Women's Hospital at 1 site in United States.
Trial summary
This study aims to determine the safety and preliminary efficacy of psilocybin-assisted psychotherapy in improving alcohol-related outcomes among adults with severe alcohol use disorder in a a double-blind, dose-comparison concurrent control, randomized trial. Read more about this study
- Who is it for?
- Ages 18 to 65 years
- Conditions the study is for
- Alcohol Use Disorder
- What is being tested?
- Psilocybin
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 36 participants
- Where
- 1 siteUnited States
- Study dates
- 15 Nov 2026to Feb 2030
- Phase
- Phase 2
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
To be eligible, individuals must be:
- English speaking adults between ages 18 and 65
- Diagnosis of DSM5 AUD, severe
- Completion of inpatient withdrawal management (i.e. "detox") for AUD within 90 days of enrollment
- Amenable to attending all psychotherapy and study visits at BWH CCI
- Able to identify an individual who can act as points of contact during the trial
- Have a friend or family member who can bring the participant home after the psilocybin sessions and stay overnight
Individuals with any of the following will be excluded:
- • Any personal history of a psychotic disorder (schizophrenia, schizoaffective disorder, brief psychotic disorder, delusional disorder, schizophreniform disorder, substance-induced psychotic disorder or major depression with psychotic features) or any bipolar-spectrum disorder
- Participants with a family history of first-degree relatives with psychotic disorder or bipolar-spectrum disorder
- Participants who have a significant suicide risk as defined by current suicidal ideation (Columbia-Suicide Severity Rating Scale (C-SSRS) score 2 to 5) and/or recent (within the past 6 months) active suicidal ideation (C-SSRS score 4 or 5)
- Participants who have a history of significant or serious adverse reaction to classic psychedelics
- Homicidality within the last six months
- History of DSM5 hallucinogen use disorder
- Positive breath alcohol level at screening
- Need for inpatient withdrawal management for alcohol at the time of screening
- Current DSM5 opioid, cocaine, stimulant or sedative/hypnotic use disorder
- Systolic blood pressure persistently above 165mmHg during screening
- History of hypersensitivity to psilocybin
- Use of psilocybin or other psychedelics with 5-HT2B activity in the prior 12 months
- Significant EKG abnormalities including QTc prolongation defined as >450 ms for men and women, or a diagnosis or family history of Long QT syndrome.
- History of any cardiac valvulopathy that raises the risk for participation as determined by the cardiology consultant
- History of intracranial mass or bleed, seizure disorder other than alcohol withdrawal seizures, liver cirrhosis, renal failure, obstructive lung disease requiring supplemental oxygen, hyperthyroidism, narrow-angle glaucoma, uncontrolled cardiac arrythmias, heart failure
- History of head trauma, stroke, or myocardial infarction in one year prior to enrollment.
- Expected to require surgical treatment at any point during the trial
- Liver dysfunction with LFTs > 3x upper normal limit at screening and Total bilirubin > 2.5x the upper normal limit
- MRI contraindications (other ferromagnetic implants, body weight greater than 550 lbs., etc.)
- Pregnant or breastfeeding
- High risk for adverse emotional or behavioral reaction based on the opinion of the study investigators such as evidence of a personality disorder
- Currently taking medications with serotonergic activity (other than SSRIs/SNRIs); inhibitors of UGT1A9, UGT1A10, MAO, and aldehyde or alcohol dehydrogenase; antipsychotics (e.g., first and second generation); mood stabilizers (e.g., lithium, valproic acid); or significant inhibitors of UGT enzymes that metabolize psilocin
- Selective serotonergic reuptake inhibitors and serotonin and norepinephrine reuptake inhibitors are allowed if participants have been on stable doses of the medication(s) for at least 90 days prior to enrollment.
- Currently receiving insulin for blood sugar management.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Zack Sager, MD contact
United States1 site
Brigham and Women's Hospital
Boston, Massachusetts, 02115
Emily A Clinical Research Project Manager, BA, MS, DNP, RN, PMHNP-BC, PMP, 6175250676, enolan4@bwh.harvard.edu
Aishwarya Senior Program Coordinator, MS, amahajan6@bwh.harvard.edu
About this study
Official title: Psilocybin-Assisted Psychotherapy for the Treatment of Severe Alcohol Use Disorder: A Double-Blind, Dose-Comparison Concurrent Control Randomized Trial
This study aims to determine the safety and preliminary efficacy of psilocybin-assisted psychotherapy in improving alcohol-related outcomes among adults with severe alcohol use disorder in a a double-blind, dose-comparison concurrent control, randomized trial. Participants will undergo structured psychotherapy and will be randomized to two psilocybin sessions to receive either a full dose (30mg or 40mg) or low dose (10mg or 15mg).
Read the detailed description
This study is a double-blind, dose-comparison concurrent control randomized trial designed to evaluate the effects of psilocybin-assisted psychotherapy on alcohol-related outcomes, neurocognitive processes related to craving and stress, and neural circuits involved in reward and regulation among adults with severe alcohol use disorder (AUD). Participants are recruited up to 3 months after completing inpatient alcohol withdrawal treatment to ensure medical stabilization prior to psilocybin administration. The study examines both preliminary efficacy and safety while also exploring mechanistic pathways through behavioral assessments and functional neuroimaging.
Participants (N=36) are randomized in a 1:1 ratio to receive either a full-dose psilocybin (30 mg, with option to escalate to 40 mg on the second session) or a low-dose (10 mg, with option to escalate to 15 mg on the second session). All participants complete two dosing sessions spaced four weeks apart. The psychotherapy is delivered by a dyad of trained therapists before, during, and after the dosing sessions and is based on established therapeutic frameworks used in prior psilocybin-assisted therapy trials. The aim of the therapeutic support is to prepare participants for the psilocybin experience, facilitate psychological processing during and after dosing, and support integration of insights into daily life. A peer recovery coach is integrated into the study to support relapse prevention, enhance coping skills, and encourage engagement in ongoing addiction treatment. All participants are offered follow-up services at the institution's outpatient addiction treatment program (including the BWH Bridge Clinic), regardless of study arm. This combination of medical oversight, psychotherapy, and recovery support reflects an effort to embed the intervention within real-world addiction care settings.
Alcohol-related outcomes are assessed repeatedly from baseline through 48 weeks after the second dosing session. The primary clinical outcome is the percentage of heavy drinking days during the 24-week follow-up period, measured using Timeline Follow-Back. Secondary alcohol outcomes include drinking quantity and frequency, relapse timing, direct alcohol biomarkers (phosphatidylethanol and ethylglucuronide), withdrawal symptoms, treatment expectancy, blinding integrity, and quality of life measures. Additional exploratory outcomes assess peer support engagement and 12-step attendance.
Safety is evaluated throughout the study using structured assessments of adverse events, vital signs, and mood and anxiety symptoms. Because participants have severe AUD and recent withdrawal treatment, careful medical screening is conducted prior to each dosing session. The study includes multiple follow-up assessments up to 48 weeks after the second psilocybin dose, allowing characterization of both acute and longer-term safety.
Two mechanistic components are incorporated. First, neurocognitive tasks assess cue-induced craving, attentional bias, stress reactivity, delayed discount, decision making, and distress tolerance. These measures evaluate whether psilocybin influences cognitive and affective processes known to contribute to alcohol use and relapse. Second, participants complete two fMRI scans-first within one week prior to the first dosing session and the second within one week after the second dosing session. The fMRI tasks evaluate neural response to alcohol-related cues and the ability to down-regulate craving, focusing on the nucleus accumbens (NAcc) and dorsolateral prefrontal cortex (DLPFC). Connectivity analyses examine changes in functional coupling between these regions during alcohol cue processing.
Together, these approaches allow the study to evaluate whether full-dose psilocybin, compared to low-dose, produces greater reductions in heavy drinking and craving, whether the treatment is safe and tolerable for individuals with severe AUD, and whether changes in cognitive, emotional, and neural functioning help explain clinical outcomes. By recruiting individuals immediately following inpatient detoxification, the study also examines the feasibility of incorporating psilocybin-assisted therapy into a critical window of early recovery. Results will inform whether a larger, fully powered clinical trial is justified and will contribute to the broader understanding of psilocybin's therapeutic potential in alcohol use disorder.
- Conditions
- Alcohol Use Disorder
- Being tested
- Psilocybin
- Keywords
- alcohol use disorder, psilocybin, inpatient withdrawal management, psychedelic
- Medical subject headings
- Alcoholism
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
PsilocybinDrug
Psilocybin is administered in oral capsule form during two dosing sessions held four weeks apart. Each session occurs in a controlled clinical environment with continuous monitoring by trained study therapists. Participants receive a standardized psychotherapy protocol that includes preparatory sessions before dosing and integration sessions afterward. The randomized dosing schedule includes either 10 mg with optional escalation to 15 mg or 30 mg with optional escalation to 40 mg for the second session. All participants also receive support from a peer recovery coach and are offered ongoing outpatient addiction treatment throughout the study period.
| Study group | Role | What they receive |
|---|---|---|
| Low Dose Psilocybin | Active comparator | Participants randomized to this arm receive psilocybin in capsule form at a dose of 10 mg during the first dosing session, with the option to increase to 15 mg at the second session. Doses are administered orally under direct supervision in a controlled clinical setting and paired with the same standardized psychotherapy protocol used in the high-dose arm. Participants complete two dosing sessions four weeks apart and receive ongoing support from a peer recovery coach and optional outpatient addiction treatment. Receives: Drug: Psilocybin |
| Full Dose Psilocybin | Experimental | Participants randomized to this arm receive psilocybin in capsule form at a dose of 30 mg during the first dosing session, with the option to increase to 40 mg at the second session. Doses are administered orally under direct supervision in a controlled clinical setting and paired with a standardized psychotherapy protocol, including preparatory and integration sessions. All participants complete two dosing sessions spaced four weeks apart and receive ongoing support from a peer recovery coach and optional outpatient addiction treatment. Receives: Drug: Psilocybin |
What is being measured
The primary outcome is the main question the study is designed to answer.
Percent Heavy Drinking Days
Percent Heavy Drinking Days (PHDD) is defined as the percentage of days in which participants engage in heavy drinking, calculated using the Timeline Follow-Back (TLFB) method. Heavy drinking is defined using NIAAA criteria (≥4 drinks/day for women; ≥5 drinks/day for men). PHDD will be analyzed as a continuous outcome to compare change over time between the full-dose and low-dose psilocybin groups.
Measured: Weeks 0-24 following the first psilocybin dosing session.
Adverse effects
We will utilize the Patient-Rated Inventory of Side Effects to assess the frequency and severity of adverse effects.
Measured: 1, 2, 4, 8, 16, 24 and 48 weeks after receiving the second dose of the psilocybin treatment.
Cue-Induced Craving Response
Craving intensity elicited by alcohol-related visual cues during a standardized cue-reactivity task as measured using a visual analog scale. The scale is titled Cue induced Craving scale and is measured from 0-10, 0 being Not at all and 10 being extremely craving. A higher score indicates more craving of the substance shown.
Measured: Measured at baseline, 4 and 24 weeks after the second psilocybin treatment.
Neural Response and Connectivity Changes measured by fMRI
BOLD response in the nucleus accumbens (NAcc) to alcohol-related images during craving.
Measured: 1 week before and 1 week after the second psilocybin session
Neural Response and Connectivity Changes measured by fMRI
BOLD response in the dorsolateral prefrontal cortex (DLPFC) during down-regulation of craving.
Measured: 1 week before and 1 week after the second psilocybin session
Neural Response and Connectivity Changes measured by fMRI
NAcc-DLPFC functional connectivity during alcohol cue processing.
Measured: 1 week before and 1 week after the second psilocybin session
Secondary outcomes (28)
Percent Days Abstinent
Percentage of days with no alcohol use, based on TLFB.
Measured: Baseline to Weeks 24
Drinks Per Drinking Day
Number of standard drinks consumed on days with any drinking, assessed using the Timeline Follow-Back (TLFB) method.
Measured: Baseline to Week 24
Vital signs
Blood pressure
Measured: Baseline to Week 48
MEQ30 - Mystical Experience Questionnaire.
The Mystical Experience Questionnaire (MEQ-30) is a 30-item self-report measure assessing the intensity of mystical-type experiences during a psychedelic session. Scores are calculated for Transcendence, Positive Mood, Ineffability, Mystical experience, and as a total score, with each expressed as a percentage of the maximum possible score. Higher percentages indicate more intense and complete mystical experiences.
Measured: Visit 6 & 10 (about 4 weeks in between visits 6 and 10)
Altered states of consciousness
5-dimensional Altered States of Consciousness questionnaire
Measured: Immediately after each drug session
Distress Tolerance
Mirror Tracing Persistence Task- Assesses distress tolerance.
Measured: Measured at baseline, 4 and 24 weeks after the second psilocybin treatment.
Days to Relapse
Number of days from first psilocybin dose to first consumption of alcohol following inpatient withdrawal treatment.
Measured: Baseline to Week 48
Days to First Heavy Drinking Day
Number of days from first psilocybin dose to first heavy drinking episode, defined using NIAAA criteria.
Measured: Baseline to Week 48
WHO Drinking Risk Level
Change in WHO alcohol risk classification categories based on self-reported alcohol consumption.
Measured: Baseline; Weeks 1, 2, 4, 8, 16, 24, and 48
Phosphatidylethanol (PEth) Levels
Blood biomarker of recent alcohol use measured via PEth concentration.
Measured: Baseline; Weeks 4, 8, 24, and 48
Ethylglucuronide (EtG) Levels
Urine biomarker of recent alcohol consumption measured via EtG levels.
Measured: Baseline; Weeks 4, 8, 24, and 48
Alcohol Withdrawal Severity
The Clinical Institute Withdrawal Assessment for Alcohol-Revised (CIWA-Ar) is a clinician-administered scale used to assess the severity of alcohol withdrawal symptoms. It includes 10 items evaluating symptoms such as tremor, anxiety, agitation, nausea, and hallucinations, with total scores ranging from 0 to 67. Higher scores indicate more severe withdrawal and guide clinical management and treatment decisions.
Measured: Baseline to Week 24
Treatment Expectancy: Set and Setting (Stanford Expectancy Treatment Scale; SETS)
Participant expectations regarding treatment benefit measured prior to any psilocybin dosing. The Stanford Expectancy Treatment Scale (SETS) is a self-report measure assessing participants' expectations, mindset ("set"), and perceptions of the treatment context ("setting") prior to an intervention. It evaluates beliefs about treatment credibility, anticipated benefits, and the therapeutic environment. Higher scores indicate more positive expectations and a more supportive perceived setting.
Measured: Visit 1- Baseline visit
Assessment of Blinding
Participant and clinician guesses regarding dose assignment to evaluate masking integrity.
Measured: Visit 6 and 10, 4 weeks between
Alcohol Craving (Penn Alcohol Craving Scale; PACS
he Penn Alcohol Craving Scale (PACS) is a 5-item self-report measure assessing the frequency, intensity, and duration of alcohol craving over the past week. Total scores range from 0 to 30. Higher scores indicate greater alcohol craving severity.
Measured: Baseline; Weeks 1, 2, 4, 8, 16, 24, and 48
Quality of Life (WHOQOL-BREF)
The World Health Organization Quality of Life-BREF (WHOQOL-BREF) is a self-report measure assessing overall quality of life across physical health, psychological health, social relationships, and environment. Scores are calculated for each domain and transformed to standardized scales. Higher scores indicate better perceived quality of life.
Measured: Baseline; Weeks 8, 24, and 48
Peer Support Engagement
Frequency and extent of interactions with the peer recovery coach across the study period.
Measured: Baseline to Week 48
12-Step Meeting Attendance
Self-reported attendance at Alcoholics Anonymous or other mutual-help meetings.
Measured: Baseline to Week 48
Depression Severity (PHQ-9)
The Patient Health Questionnaire-9 (PHQ-9) is a 9-item self-report measure assessing depressive symptom severity over the past two weeks. Total scores range from 0 to 27. Higher scores indicate greater severity of depressive symptoms.
Measured: Baseline to Week 48
Anxiety Severity (GAD-7)
The Generalized Anxiety Disorder-7 (GAD-7) is a 7-item self-report measure assessing anxiety symptom severity over the past two weeks. Total scores range from 0 to 21. Higher scores indicate greater anxiety severity
Measured: Baseline to Week 48
Suicidality (C-SSRS)
The Columbia-Suicide Severity Rating Scale (C-SSRS) is a clinician-administered measure assessing the severity and intensity of suicidal ideation and behavior. It evaluates the presence, frequency, and lethality of suicidal thoughts and actions over specified time frames. Higher severity ratings indicate greater suicide risk and inform clinical monitoring and intervention.
Measured: Baseline to Week 48
Liver Function Tests
Laboratory evaluation of hepatic safety using standard liver enzyme markers.
Measured: Baseline; routine follow-up through Week 48
Hospital Readmission
Documentation of any all-cause hospital readmissions during the follow-up period.
Measured: Baseline to Week 48
Attentional Bias to Alcohol Cues (Visual Probe Task)
Baseline; Weeks 4 and 24 after the second psilocybin session
Measured: Assessed using the Visual Probe Task (VPT), which measures attentional bias through reaction time differences when responding to probes replacing alcohol-related vs. neutral stimuli.
Delayed Discounting (Monetary Choice Questionnaire)
Measured using the Monetary Choice Questionnaire, which presents choices between smaller immediate rewards and larger delayed rewards. The calculated discount rate (k-value) reflects impulsive choice and reward valuation.
Measured: Baseline; Weeks 4 and 24 after the second psilocybin session
Decision-Making Performance (Iowa Gambling Task)
Measured using the Iowa Gambling Task (IGT). Participants select cards from decks with varying reward and penalty structures. Performance reflects learning from feedback and risk-sensitive decision making.
Measured: Baseline; Weeks 4 and 24 after the second psilocybin session
Vital signs
Heart rate will be measured.
Measured: Baseline to Week 48
Vital signs
Temperature will be measured.
Measured: Baseline to Week 48
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Dec 2025
- Study start15 Nov 2026 (estimated)
- Primary completion1 Dec 2029 (estimated)
- Study completionFeb 2030 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Alcohol Use DisorderStudies of the same condition, open and under way.
- More trials run by Brigham and Women's HospitalThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- This study uses a double-blind, parallel-group, dose-comparison concurrent control, randomized trial design. Participants are randomly assigned in a 1:1 ratio to receive two sessions of either a full dose (30 mg with optional escalation to 40 mg) or a low dose (10 mg with optional escalation to 15 mg). All participants receive two dosing sessions four weeks apart, along with a standardized psychotherapy protocol delivered before, during, and after each session. Outcomes are assessed repeatedly from baseline through 48 weeks after the second dose, allowing evaluation of both clinical effects and mechanistic changes over time.
- Masking
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 36 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Brigham and Women's Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Joji Suzuki, MD, Brigham and Women's Hospital
- Investigators
- Joji Suzuki, MD, Principal investigator, Brigham and Women's Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07296094
- Sponsor's protocol ID
- 2025P002909
- Status last verified
- Oct 2026
- First submitted
- 12 Dec 2025
- Last updated
- 9 Oct 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 9 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Psilocybin-Assisted Psychotherapy for the Treatment of Severe Alcohol Use Disorder: A Double-Blind, Dose-Comparison Concurrent Control Randomized Trial
- ClinicalTrials.gov ID
- NCT07296094
- Acronym / sponsor ID
- 2025P002909
- Conditions
- Alcohol Use Disorder
- Keywords
- alcohol use disorder, psilocybin, inpatient withdrawal management, psychedelic
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 36 participants (estimated)
- Lead sponsor
- Brigham and Women's HospitalUniversity, hospital or other
- Study start
- 15 Nov 2026 (estimated)
- Primary completion
- 1 Dec 2029 (estimated)
- Study completion
- Feb 2030 (estimated)
- First posted
- 22 Dec 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study aims to determine the safety and preliminary efficacy of psilocybin-assisted psychotherapy in improving alcohol-related outcomes among adults with severe alcohol use disorder in a a double-blind, dose-comparison concurrent control, randomized trial. Participants will undergo structured psychotherapy and will be randomized to two psilocybin sessions to receive either a full dose (30mg or 40mg) or low dose (10mg or 15mg).
Detailed description
This study is a double-blind, dose-comparison concurrent control randomized trial designed to evaluate the effects of psilocybin-assisted psychotherapy on alcohol-related outcomes, neurocognitive processes related to craving and stress, and neural circuits involved in reward and regulation among adults with severe alcohol use disorder (AUD). Participants are recruited up to 3 months after completing inpatient alcohol withdrawal treatment to ensure medical stabilization prior to psilocybin administration. The study examines both preliminary efficacy and safety while also exploring mechanistic pathways through behavioral assessments and functional neuroimaging.
Participants (N=36) are randomized in a 1:1 ratio to receive either a full-dose psilocybin (30 mg, with option to escalate to 40 mg on the second session) or a low-dose (10 mg, with option to escalate to 15 mg on the second session). All participants complete two dosing sessions spaced four weeks apart. The psychotherapy is delivered by a dyad of trained therapists before, during, and after the dosing sessions and is based on established therapeutic frameworks used in prior psilocybin-assisted therapy trials. The aim of the therapeutic support is to prepare participants for the psilocybin experience, facilitate psychological processing during and after dosing, and support integration of insights into daily life. A peer recovery coach is integrated into the study to support relapse prevention, enhance coping skills, and encourage engagement in ongoing addiction treatment. All participants are offered follow-up services at the institution's outpatient addiction treatment program (including the BWH Bridge Clinic), regardless of study arm. This combination of medical oversight, psychotherapy, and recovery support reflects an effort to embed the intervention within real-world addiction care settings.
Alcohol-related outcomes are assessed repeatedly from baseline through 48 weeks after the second dosing session. The primary clinical outcome is the percentage of heavy drinking days during the 24-week follow-up period, measured using Timeline Follow-Back. Secondary alcohol outcomes include drinking quantity and frequency, relapse timing, direct alcohol biomarkers (phosphatidylethanol and ethylglucuronide), withdrawal symptoms, treatment expectancy, blinding integrity, and quality of life measures. Additional exploratory outcomes assess peer support engagement and 12-step attendance.
Safety is evaluated throughout the study using structured assessments of adverse events, vital signs, and mood and anxiety symptoms. Because participants have severe AUD and recent withdrawal treatment, careful medical screening is conducted prior to each dosing session. The study includes multiple follow-up assessments up to 48 weeks after the second psilocybin dose, allowing characterization of both acute and longer-term safety.
Two mechanistic components are incorporated. First, neurocognitive tasks assess cue-induced craving, attentional bias, stress reactivity, delayed discount, decision making, and distress tolerance. These measures evaluate whether psilocybin influences cognitive and affective processes known to contribute to alcohol use and relapse. Second, participants complete two fMRI scans-first within one week prior to the first dosing session and the second within one week after the second dosing session. The fMRI tasks evaluate neural response to alcohol-related cues and the ability to down-regulate craving, focusing on the nucleus accumbens (NAcc) and dorsolateral prefrontal cortex (DLPFC). Connectivity analyses examine changes in functional coupling between these regions during alcohol cue processing.
Together, these approaches allow the study to evaluate whether full-dose psilocybin, compared to low-dose, produces greater reductions in heavy drinking and craving, whether the treatment is safe and tolerable for individuals with severe AUD, and whether changes in cognitive, emotional, and neural functioning help explain clinical outcomes. By recruiting individuals immediately following inpatient detoxification, the study also examines the feasibility of incorporating psilocybin-assisted therapy into a critical window of early recovery. Results will inform whether a larger, fully powered clinical trial is justified and will contribute to the broader understanding of psilocybin's therapeutic potential in alcohol use disorder.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 2
- Model description
- This study uses a double-blind, parallel-group, dose-comparison concurrent control, randomized trial design. Participants are randomly assigned in a 1:1 ratio to receive two sessions of either a full dose (30 mg with optional escalation to 40 mg) or a low dose (10 mg with optional escalation to 15 mg). All participants receive two dosing sessions four weeks apart, along with a standardized psychotherapy protocol delivered before, during, and after each session. Outcomes are assessed repeatedly from baseline through 48 weeks after the second dose, allowing evaluation of both clinical effects and mechanistic changes over time.
| Arm | Type | Receives |
|---|---|---|
| Low Dose Psilocybin | Active comparator | Drug: PsilocybinParticipants randomized to this arm receive psilocybin in capsule form at a dose of 10 mg during the first dosing session, with the option to increase to 15 mg at the second session. Doses are administered orally under direct supervision in a controlled clinical setting and paired with the same standardized psychotherapy protocol used in the high-dose arm. Participants complete two dosing sessions four weeks apart and receive ongoing support from a peer recovery coach and optional outpatient addiction treatment. |
| Full Dose Psilocybin | Experimental | Drug: PsilocybinParticipants randomized to this arm receive psilocybin in capsule form at a dose of 30 mg during the first dosing session, with the option to increase to 40 mg at the second session. Doses are administered orally under direct supervision in a controlled clinical setting and paired with a standardized psychotherapy protocol, including preparatory and integration sessions. All participants complete two dosing sessions spaced four weeks apart and receive ongoing support from a peer recovery coach and optional outpatient addiction treatment. |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| PsilocybinPsilocybin is administered in oral capsule form during two dosing sessions held four weeks apart. Each session occurs in a controlled clinical environment with continuous monitoring by trained study therapists. Participants receive a standardized psychotherapy protocol that includes preparatory sessions before dosing and integration sessions afterward. The randomized dosing schedule includes either 10 mg with optional escalation to 15 mg or 30 mg with optional escalation to 40 mg for the second session. All participants also receive support from a peer recovery coach and are offered ongoing outpatient addiction treatment throughout the study period. | Drug | Full Dose Psilocybin, Low Dose Psilocybin |
Primary outcome
Percent Heavy Drinking Days
Time frame: Weeks 0-24 following the first psilocybin dosing session.
Percent Heavy Drinking Days (PHDD) is defined as the percentage of days in which participants engage in heavy drinking, calculated using the Timeline Follow-Back (TLFB) method. Heavy drinking is defined using NIAAA criteria (≥4 drinks/day for women; ≥5 drinks/day for men). PHDD will be analyzed as a continuous outcome to compare change over time between the full-dose and low-dose psilocybin groups.
Adverse effects
Time frame: 1, 2, 4, 8, 16, 24 and 48 weeks after receiving the second dose of the psilocybin treatment.
We will utilize the Patient-Rated Inventory of Side Effects to assess the frequency and severity of adverse effects.
Cue-Induced Craving Response
Time frame: Measured at baseline, 4 and 24 weeks after the second psilocybin treatment.
Craving intensity elicited by alcohol-related visual cues during a standardized cue-reactivity task as measured using a visual analog scale. The scale is titled Cue induced Craving scale and is measured from 0-10, 0 being Not at all and 10 being extremely craving. A higher score indicates more craving of the substance shown.
Neural Response and Connectivity Changes measured by fMRI
Time frame: 1 week before and 1 week after the second psilocybin session
BOLD response in the nucleus accumbens (NAcc) to alcohol-related images during craving.
Neural Response and Connectivity Changes measured by fMRI
Time frame: 1 week before and 1 week after the second psilocybin session
BOLD response in the dorsolateral prefrontal cortex (DLPFC) during down-regulation of craving.
Neural Response and Connectivity Changes measured by fMRI
Time frame: 1 week before and 1 week after the second psilocybin session
NAcc-DLPFC functional connectivity during alcohol cue processing.
28 secondary outcomes
Percent Days Abstinent
Time frame: Baseline to Weeks 24
Drinks Per Drinking Day
Time frame: Baseline to Week 24
Vital signs
Time frame: Baseline to Week 48
MEQ30 - Mystical Experience Questionnaire.
Time frame: Visit 6 & 10 (about 4 weeks in between visits 6 and 10)
Altered states of consciousness
Time frame: Immediately after each drug session
Distress Tolerance
Time frame: Measured at baseline, 4 and 24 weeks after the second psilocybin treatment.
Days to Relapse
Time frame: Baseline to Week 48
Days to First Heavy Drinking Day
Time frame: Baseline to Week 48
WHO Drinking Risk Level
Time frame: Baseline; Weeks 1, 2, 4, 8, 16, 24, and 48
Phosphatidylethanol (PEth) Levels
Time frame: Baseline; Weeks 4, 8, 24, and 48
Ethylglucuronide (EtG) Levels
Time frame: Baseline; Weeks 4, 8, 24, and 48
Alcohol Withdrawal Severity
Time frame: Baseline to Week 24
Treatment Expectancy: Set and Setting (Stanford Expectancy Treatment Scale; SETS)
Time frame: Visit 1- Baseline visit
Assessment of Blinding
Time frame: Visit 6 and 10, 4 weeks between
Alcohol Craving (Penn Alcohol Craving Scale; PACS
Time frame: Baseline; Weeks 1, 2, 4, 8, 16, 24, and 48
Quality of Life (WHOQOL-BREF)
Time frame: Baseline; Weeks 8, 24, and 48
Peer Support Engagement
Time frame: Baseline to Week 48
12-Step Meeting Attendance
Time frame: Baseline to Week 48
Depression Severity (PHQ-9)
Time frame: Baseline to Week 48
Anxiety Severity (GAD-7)
Time frame: Baseline to Week 48
Suicidality (C-SSRS)
Time frame: Baseline to Week 48
Liver Function Tests
Time frame: Baseline; routine follow-up through Week 48
Hospital Readmission
Time frame: Baseline to Week 48
Attentional Bias to Alcohol Cues (Visual Probe Task)
Time frame: Assessed using the Visual Probe Task (VPT), which measures attentional bias through reaction time differences when responding to probes replacing alcohol-related vs. neutral stimuli.
Delayed Discounting (Monetary Choice Questionnaire)
Time frame: Baseline; Weeks 4 and 24 after the second psilocybin session
Decision-Making Performance (Iowa Gambling Task)
Time frame: Baseline; Weeks 4 and 24 after the second psilocybin session
Vital signs
Time frame: Baseline to Week 48
Vital signs
Time frame: Baseline to Week 48
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 9 Oct 2026.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Zack Sager, MD contact
Joji Suzuki, MD principal investigator
Brigham and Women's Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing Psilocybin in people with Alcohol Use Disorder, run by Brigham and Women's Hospital at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 9 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Joji Suzuki, MD (617-732-5752, jsuzuki2@bwh.harvard.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Percent Heavy Drinking Days (time frame: Weeks 0-24 following the first psilocybin dosing session.). The study lists 6 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Oct 2026; AzTrials last refreshed its copy on 26 Oct 2026.