Psilocybin for Treatment-Resistant Depression in Veterans
Official title: A Multi-site Randomized Controlled Trial of Psilocybin for Treatment-Resistant Depression (TRD) in Veterans
Run by VA Office of Research and Development · NCT07226232 · Data updated 2026-11-12
This study tests whether psilocybin can help U.S. military veterans with treatment-resistant depression, with or without PTSD.
Quick facts
| Phase | Phase 3 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years to 75 Years |
| Sex | All |
| Enrollment | 240 (estimated) |
| Sponsor | VA Office of Research and Development Federal |
| Locations | 5 sites (Birmingham, Alabama and 4 other locations) |
| Status | Recruiting |
| Started | August 3, 2026 |
| Main results expected | December 2, 2030 |
| Study ends | June 30, 2031 |
| Registry record updated | October 23, 2026 |
| Trial ID | NCT07226232 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
U.S. military veterans up to 75 years old with Major Depressive Disorder and inadequate response to at least two antidepressants, including those with stable comorbid PTSD.
✕Probably not a fit
Patients who do not experience sufficient symptom improvement or who encounter intolerable adverse effects may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This multi-site, double-blind randomized trial will compare two psilocybin doses given across two sessions, with preparation, administration, and integration support, in Veterans who meet criteria for major depressive disorder. Outcomes are assessed by independent evaluators at 2 and 4 weeks after each dosing session, with follow-up extended to 6 months. The study also monitors safety and adverse events related to the drug. Eligible participants include English-speaking veterans up to age 75 who have failed multiple antidepressant treatments and meet DSM-5 criteria for current major depressive episode. The research is conducted at VA medical centers in Alabama and Oregon and is sponsored by the VA Office of Research and Development.
Why it matters
Potential benefit: If successful, psilocybin could offer a new treatment option for veterans with TRD, potentially reducing depressive symptoms and improving quality of life.
How similar studies have gone: Previous civilian studies suggest antidepressant effects of psilocybin, but data in veterans and those with PTSD are limited and earlier findings are not yet definitive.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * 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 Exclusion Criteria: * 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
Where it's running
-
Birmingham VA Medical Center, Birmingham, AL
Birmingham, Alabama, United States Recruiting -
Tuscaloosa VA Medical Center, Tuscaloosa, AL
Tuscaloosa, Alabama, United States Recruiting -
VA Portland Health Care System, Portland, OR
Portland, Oregon, United States Recruiting -
Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA
Philadelphia, Pennsylvania, United States Recruiting -
VA Puget Sound Health Care System Seattle Division, Seattle, WA
Seattle, Washington, United States Recruiting
Study contacts
- Principal investigator: Lori Lynne Davis, MD AB — Birmingham VA Medical Center, Birmingham, AL
- Study coordinator: Lori L Davis, MD AB
- Email: lori.davis@va.gov
- Phone: (205) 554-3819
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Can tACS modulate motivation and reward signals in cannabis use disorder and depression
We’re testing whether a gentle brain stimulation method (tACS) can boost motivation and reward responses in adults with cannabis use and/or depression to see if it helps with anhedonia.
-
Neural links for real-world emotions in mood and anxiety
Researchers are testing how real-life emotional moments relate to brain activity and stress responses in young adults with mood and anxiety symptoms, using smartphones, self-reports, tasks, and MRI.
-
EEG-Guided TMS for Adults With Depression
This study tests whether delivering intermittent theta burst stimulation (iTBS) timed to brain waves using EEG can improve treatment for adults with major depressive disorder who have not responded to usual antidepressants.
-
iTBS to help anhedonia in depression (dual left DLPFC + OFC or left DLPFC alone)
A brain stimulation study tests whether intermittent theta burst stimulation can help people with major depression who have anhedonia, using both dual-target (left DLPFC and OFC) and single-target (left DLPFC) approaches.
-
One Day of Ultra-Accelerated TMS With a Dose of NRX-101 for Major Depression
This study tests whether a single day of rapid TMS plus NRX-101 can help people with moderate to severe depression see improvement over six weeks.
-
EEG microstates and inflammatory markers in treatment-resistant depression patients undergoing ECT
This study tests how electroconvulsive therapy affects brain activity patterns seen in EEG and inflammatory biomarkers in adults with treatment-resistant major depression.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.