Psilocybin Intervention for Veterans Overcoming Treatment-Resistant Depression

Starting soon · Phase 3

Conditions studied: Major Depression

In brief

The purpose of this multi-site randomized controlled trial is to evaluate the efficacy and risks of psilocybin for the treatment of depression in U.S. military Veterans with and without (±) concurrent posttraumatic stress disorder.

Key facts

Study ID

NCT07226232

Run by

VA Office of Research and Development

People needed

240

Starts

2026-07-30

Expected to finish

2031-06-30

Last updated by the study team

2026-06-05

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Veteran of the U.S. military who is English-speaking
• Signed informed consent and HIPAA
• Adults </= 75 years of age
• Meets DSM-5 criteria for current major depressive episode (MDE)
• MADRS >/= 20 at baseline
• Failure to respond satisfactorily to >/= 2 antidepressant treatments for >/= 8 weeks, including >/= 2 weeks at an adequate dose (>/= 50% of the FDA-approved uppermost dose) for major depression. Augmentation with a medication for depression (e.g., neuroleptics, lithium, levothyroxine) is considered a separate course of treatment.
• If applicable, concurrent \& permitted antidepressants must be at stable doses for >/= 4 weeks prior to baseline (see allowed \& prohibited medication list)
• Participants of child-bearing potential must have negative pregnancy test \& agree to adhere to a medically acceptable method of birth control during the study
• Has a responsible adult who will provide transportation to the participant's home or place of lodging on the days of psilocybin administration

You may not qualify if…

• Lifetime bipolar, schizophrenia spectrum, or other psychotic disorders
• First-degree relative with history of bipolar I, schizophrenia spectrum or other psychotic disorder
• Presence of psychotic symptoms (e.g., MDE with psychotic symptoms)
• Sedative-hypnotic, stimulant, inhalant and/or opioid use disorder within past 6 months (lifetime substance use disorder is allowed at the discretion of the LSI)
• Severe alcohol and/or cannabis use disorder within the past 6 months (mild or moderate alcohol and/or cannabis use is allowed at the discretion of the LSI)
• Lifetime hallucinogen persisting perception or hallucinogen use disorders
• Use of psilocybin, ayahuasca, mescaline, lysergic acid diethylamide (LSD), dimethyltryptamine (DMT), 5-Methoxy-N,N-dimethyltryptamine (5-MeO-DMT), peyote, or 3,4-methylenedioxymethamphetamine (MDMA) within past 6 months
• Participant agrees to not use psychedelics (listed above) during the study, except as prescribed by the study protocol
• Taking prohibited medication within 2 weeks of baseline (see allowed and prohibited concomitant medication list)
• History of severe traumatic brain injury (TBI)
• Diagnosis of dementia or related progressive neurocognitive disorder
• Suicidal ideation/behavior Type 4 or Type 5 intensity on C-SSRS within past 6 months of baseline
• Psychiatric inpatient treatment within past 3 months of baseline
• Treatment with electroconvulsive therapy, deep brain stimulation, vagus nerve stimulation, or transcranial magnetic stimulation within 3 months of baseline
• Implanted central nervous system device
• Treatment with evidence-based psychotherapy (EBP) for MDD or PTSD within 2 weeks prior to baseline. If receiving EBP therapy, he/she must complete treatment at least 2 weeks prior to baseline. Other forms of non-EBP psychotherapy for MDD or PTSD are allowed to continue during the study period.
• Pregnancy or lactation, or anticipated pregnancy or breastfeeding during the active treatment phase
• History of myocardial infarction, congestive heart failure, diabetic ketoacidosis, brain cancer, stroke and/or severe cardiac disease
• Clinically significant cardiac, pulmonary, renal, liver and/or other medical disease that, in the opinion of the investigator, may contraindicate the use of psilocybin, interfere with the interpretation of study results and/or constitute a health risk for the participant if they take part in the study
• Seizure disorder, except for seizures due to fever or withdrawal from a substance
• Clinically significant hypertension (>160/95 mmHg), hypotension (<90/60 mmHg) tachycardia (>100 bpm at rest), QTc prolongation (>450 msec men; >470 msec women) or clinically significant arrhythmia on ECG
• Clinically significant abnormal laboratory results on chemistry panel, liver function tests, complete blood count, and/or thyroid stimulating hormone
• Positive urine drug screen for illicit drugs of abuse (except for THC) at screening or baseline
• Prior allergic, adverse reaction or adverse experience to a psilocybin formulation
• Litigating for disability income for a mental disorder outside the VA compensation and pension process

Where it is running

• Birmingham VA Medical Center, Birmingham, AL — Birmingham, Alabama, United States
• Tuscaloosa VA Medical Center, Tuscaloosa, AL — Tuscaloosa, Alabama, United States
• VA Portland Health Care System, Portland, OR — Portland, Oregon, United States
• Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA — Philadelphia, Pennsylvania, United States
• VA Puget Sound Health Care System Seattle Division, Seattle, WA — Seattle, Washington, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.