What this study is
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.
What's being tested
- Psilocybin
Intervention · DRUG
Psilocybin comparator dose
- Psilocybin
Intervention · DRUG
Psilocybin Intervention Dose
Study details
- Official title
- A Multi-site Randomized Controlled Trial of Psilocybin for Treatment-Resistant Depression (TRD) in Veterans
- Sponsor
- VA Office of Research and Development
- Conditions
- Major Depression
- Enrolling
- 240 people
- Starts
- 2026-08-03
- Est. completion
- 2031-06-30
- Design
- Quadruple-blind, randomized, parallel groups, Phase 3
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 18 Years – 75 YearsSex ALLHealthy volunteers Not acceptedYou may qualify if
- Veteran of the U.S. military who is English-speaking
- Signed informed consent and Health Insurance Portability and Accountability Act (HIPAA)
- Adults </= 75 years of age
- Meets DSM-5 criteria for current major depressive episode (MDE)
- Montgomery-Asberg Rating Scale (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 can't join 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 XX 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
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (5)
5 openBirmingham VA Medical Center, Birmingham, AL
Birmingham, Alabama, United States
- Lori L Davis, MD AB · Contact(205) 554-3819lori.davis@va.gov
- Anchal Ghera, MS · Contact(205) 899-1273anchal.ghera@va.gov
- Lori Lynne Davis, MD AB · Principal investigator
RecruitingTuscaloosa VA Medical Center, Tuscaloosa, AL
Tuscaloosa, Alabama, United States
- Patricia Pilkinton, MD · Contact205-554-2000 ext. 4392
- Kaleb Murry, MS · Contact2055542000 ext. 4392kaleb.murry@va.gov
RecruitingVA Portland Health Care System, Portland, OR
Portland, Oregon, United States
- Christopher Stauffer, MD · Contact971-710-6204
- Audrey Shoultz, MS · Contact9717106204audrey.shoultz@va.gov
RecruitingCorporal Michael J. Crescenz VA Medical Center, Philadelphia, PA
Philadelphia, Pennsylvania, United States
- Michael Thase, MD · Contact215-823-5903michael.thase@va.gov
- Mora Grehl, PhD · Contact2158235800 ext. 20-7888
RecruitingVA Puget Sound Health Care System Seattle Division, Seattle, WA
Seattle, Washington, United States
- Rebecca Hendrickson, MD · Contact206-277-1337rebecca.hendrickson@va.gov
- Renata Daniels, MS · Contact2062771337
Recruiting
Study team
Sponsor
VA Office of Research and Development
Study ID MHBC-002-25S
Principal investigator
Lori Lynne Davis, MD AB
Birmingham VA Medical Center, Birmingham, AL
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.