Veterans
Veterans carry an unusually heavy burden of PTSD, depression, traumatic brain injury, moral injury and suicidality, and many do not respond to standard treatment. That unmet need has put them at the centre of psychedelic research, and of an intense real-world demand. The evidence is genuinely promising but still early and mostly uncontrolled, and in 2024 the US FDA declined to approve MDMA-assisted therapy for PTSD.
Data updated
Key Insights
- 1
Veterans' high burden of PTSD, depression, traumatic brain injury and suicidality, often resistant to standard care, has placed them at the centre of psychedelic research and of intense real-world demand.
- 2
MDMA-assisted therapy showed large effects in early veteran PTSD trials, but in August 2024 the FDA declined to approve it and asked for another study, citing efficacy, blinding and conduct concerns. It is promising and contested, not approved.
- 3
The largest, best-controlled ketamine trial in veterans with PTSD (158 participants) was negative for PTSD, even though ketamine helps veteran depression. It is a caution against reading small open-label successes as proof.
- 4
Psilocybin produced a strong early response in a veteran treatment-resistant-depression pilot, but the benefit waned by 12 months. The single-dose 'cure' framing is not supported by the data.
- 5
Many Special Operations veterans travel abroad for ibogaine and 5-MeO-DMT. The reported benefits are striking but come from uncontrolled, self-funded settings, and ibogaine carries a real risk of fatal cardiac arrhythmia.
By the numbers
- 31
- Trials tracked
- 52
- Papers tracked
- 1,268
- Trial participants
as of June 2026
as of June 2026
as of June 2026
What is Veterans?
Veterans face higher rates of post-traumatic stress disorder, depression, traumatic brain injury, chronic pain and suicide than the general population, driven by combat exposure, repeated deployments, military sexual trauma and the difficulty of returning to civilian life. The US Department of Veterans Affairs estimates that about 7 in 100 veterans will have PTSD in their lifetime[1], with substantially higher rates after combat, and veteran suicide remains well above the civilian rate.
Standard treatments work for many veterans but not all: a large minority stay symptomatic despite trauma-focused therapy and medication, and dropout is high. That treatment-resistance, combined with a strong sense among many veterans that existing care has not served them, is what has made this population both a focus of formal psychedelic trials and the source of a striking grassroots movement to seek these compounds wherever they can be found.
Current Treatments
First-line care for veteran PTSD is trauma-focused psychotherapy, mainly prolonged exposure and cognitive processing therapy, alongside the two SSRIs approved for PTSD (sertraline and paroxetine) or off-label SNRIs. Depression is treated with antidepressants and psychotherapy, and esketamine is approved for treatment-resistant depression. Traumatic brain injury and chronic pain are managed symptomatically.
These treatments help many people, but a substantial share of veterans remain symptomatic and many disengage from care. That gap, rather than any claim that psychedelics have closed it, is the honest starting point for this page: psychedelic-assisted approaches are being tested precisely because the unmet need is large and persistent.
This report summarises what Blossom’s database shows about psychedelic research in and for military veterans, and what it does not show. The short version: veterans carry a heavy, often treatment-resistant burden of PTSD, depression, traumatic brain injury and suicidality, which has made them central to psychedelic science and to a remarkable real-world demand. The early signals are genuinely encouraging. They are also mostly uncontrolled, the durability is shakier than the headlines, and in 2024 the most advanced programme, MDMA for PTSD, was rejected by the FDA. Both halves of that matter.
A note before the evidence
This page is a research summary, not medical advice, and nothing here is a treatment recommendation. Psychedelics are being studied in veterans; with the partial exception of esketamine for treatment-resistant depression, they are not approved treatments for these conditions, and several carry real risks. If you are a veteran or care for one, decisions about treatment belong with a qualified clinician, and travelling abroad for unregulated treatment carries safety and legal risks worth taking seriously.
One framing point on the numbers. Blossom currently tracks 51 papers and 31 trials tagged to this topic, and those counts appear on this page. They are broader than they look: the tag is leaky, pulling in cost-effectiveness models, ethics statements, mixed civilian-and-veteran retreat studies and even military drug-research history. The genuinely veteran-treatment core is a smaller subset, and the rigorously controlled part of it is a handful of trials. Read the counts as database coverage, not as a tally of proven veteran treatments.
Why are veterans central to psychedelic research?
The simplest answer is unmet need. Veterans develop PTSD, depression, traumatic brain injury and chronic pain at higher rates than civilians, and the VA estimates around 7 in 100 veterans will have PTSD in their lifetime[1], far more after combat, while veteran suicide stays well above the civilian rate. First-line treatments, trauma-focused therapy and antidepressants, help many but leave a large minority symptomatic, and dropout is high.
That gap has made veterans both a priority population for formal trials and the engine of a grassroots movement. The result is a literature with an unusual shape: a few rigorous trials sitting alongside a large body of open-label pilots, retreats and treatment-abroad cohorts, all pointing at the same desperate need from very different levels of evidence. It is also a population whose suffering is bound up with identity, duty and a sense that the institutions meant to help fell short, which is part of why interest in these treatments runs so high, and why the honesty of how they are described matters so much.
MDMA and PTSD: large effects, and a regulatory rejection
MDMA-assisted therapy is where the controlled veteran evidence is strongest and where the field hit its hardest wall. A randomised Phase 2 dose-response trial in 26 veterans, firefighters and police[2] reported a very large PTSD reduction at the 75 mg dose, a pooled analysis of six Phase 2 trials[3] found benefits that held to a year, and a meta-analysis put the pooled effect at a large magnitude[4] while rating the underlying trials only moderate in quality.
Then, in August 2024, the FDA declined to approve MDMA-assisted therapy for PTSD[5], issuing a Complete Response Letter and requesting an additional Phase 3 study. The decision crystallised the field’s structural weakness: because MDMA produces unmistakable effects, participants and therapists usually know who received it, so functional unblinding can inflate apparent benefit, and the programme also drew scrutiny over trial conduct. The proposed mechanism, oxytocin release and a shift in fear processing that eases emotional engagement[6], is plausible and supported by imaging, but a plausible mechanism is not a regulatory approval.
Ketamine: clear for depression, unclear for PTSD
Ketamine is the most-used compound in veteran care and the most instructive. For depression it performs well: a dose-finding RCT in veterans with late-life treatment-resistant depression[7] showed strong, sustained response, and repeated infusions help veterans with comorbid PTSD and depression, though the effect relapses within weeks[8].
For PTSD the story is more sobering. The single largest, best-controlled veteran trial, a multi-site RCT in 158 veterans and service members, found no PTSD benefit over placebo[9], even though it improved depression. That negative result sits in direct tension with smaller, uncontrolled combat-veteran series reporting big drops[10], and it is the cleanest illustration on this page of why open-label success is not proof.
Psilocybin: a promising signal that wanes
Psilocybin in veterans is early and honest about its own limits. The first open-label pilot in 15 veterans with severe treatment-resistant depression[11] reported 60% response and 53% remission at three weeks, a striking result for a single dose. But the 12-month follow-up showed the antidepressant effect beginning to wane by six months[12], with response down to 40% at a year.
A separate uncontrolled psilocybin retreat in 21 veterans with a history of TBI[13] reported large symptom reductions and EEG changes, and veteran PTSD trials of psilocybin are mostly still recruiting. A recurring and useful finding across these pilots is that the intensity of the acute psychedelic experience did not predict who got better, which complicates the popular idea that the subjective "trip" is the active ingredient.
Ibogaine, 5-MeO-DMT and the journey abroad
The most distinctive veteran story in this database is not a trial at all: it is the movement of Special Operations veterans who travel to clinics in Mexico for ibogaine, often followed by 5-MeO-DMT. A retrospective survey of 51 such veterans[14] reported very large before-after reductions in suicidal ideation, PTSD and depression; a larger prospective follow-up of 86 veterans[15] found the same direction of effect, and a subset with risky drinking mostly returned to non-risky levels within a month[16].
These numbers are the largest on the page and rest on the weakest designs: retrospective, self-selected, self-funded, unblinded, no control group. They are best read as powerful evidence of unmet need and self-reported relief, not as proof of efficacy. The most rigorous ibogaine work, the Stanford open-label study of magnesium-ibogaine in 30 veterans with TBI[17], is more credible but still single-arm, and even there the mystical intensity of the experience tracked with PTSD improvement[18], the opposite of the psilocybin finding above, leaving the mechanism genuinely open. Ibogaine’s risk of fatal cardiac arrhythmia is real, which is why magnesium is co-administered. Two further cautions belong here: the most-cited cohort is almost entirely white, male Special Operations veterans, so even its self-reported benefits may not carry over to the broader, more diverse veteran population, and ibogaine remains illegal in the United States, which is why this treatment happens abroad in the first place.
Substance use and suicidality
Substance use and suicidality run through the veteran story, and the data follow the same pattern: striking but uncontrolled. In the Special Operations cohorts treated abroad, a subset with risky drinking mostly returned to non-risky levels within a month[16], and the same surveys reported large reductions in suicidal ideation[14] alongside the PTSD and depression changes. The honest reading is that these compounds may help the addiction and despair that so often accompany veteran trauma, but the evidence is self-reported and uncontrolled, and nothing here establishes that they reduce suicide risk in the way a controlled trial would need to show. For a population with an elevated suicide rate, that distinction is not academic.
Moral injury and the gaps
Moral injury, the lasting harm of having done or witnessed something that violates one’s deepest values, is central to how many veterans describe their suffering, yet it is almost absent as a measured outcome in this database. Only one trial names it explicitly, and no completed study reports a moral-injury endpoint. It is an honest gap worth stating plainly: the concept that may matter most to veterans is the one the evidence has barely touched.
The trial pipeline
The forward signal is a broad pipeline: a Phase 3 psilocybin study for veteran treatment-resistant depression, multiple MDMA trials in group and massed-exposure formats, ketamine studies for comorbid pain and depression, and the magnesium-ibogaine line for TBI, with the VA increasingly funding and hosting the work. The honest counterweight is attrition: several MDMA-in-veterans trials have been terminated or withdrawn, a few are of unknown status, and the most rigorous ketamine PTSD trial was negative. A wide pipeline is a sign of momentum, not of settled answers.
Reading this honestly
So where does that leave a veteran, a clinician or a policymaker reading this? The substance is real: a population with enormous unmet need, large early effects for MDMA, solid depression results for ketamine, an encouraging psilocybin signal, and a grassroots movement that has surfaced genuine reported relief. The hype is anything implying proven, approved, durable cures. The most advanced programme was rejected, the best-controlled PTSD trial was negative, the psilocybin benefit fades, and the most dramatic numbers are uncontrolled. Taking the promise seriously while refusing to overstate it is the honest position, and for a population this vulnerable, it is the only responsible one.
Psychedelic Effect Matrix
Compound efficacy and evidence levels for Veterans.
| Compound | Magnitude | Evidence | Consistency |
|---|---|---|---|
| MDMA Large effects in early veteran and first-responder Phase 2 PTSD trials, but FDA-rejected in 2024 over efficacy, blinding and trial-conduct concerns. Promising and contested, not approved. | Large | Moderate | Moderate |
| Ketamine Helps veteran depression and TRD (including an RCT), but the largest veteran PTSD RCT (158 participants) was negative and benefits relapse within weeks. Esketamine is approved for TRD, not PTSD. | Medium | Moderate | Low |
| Psilocybin One open-label veteran TRD pilot (15 participants) showed a strong early response that waned by 12 months. No veteran randomised trial yet. Promising but preliminary. | Medium | Low | Low |
| Ibogaine Striking before-after improvements in uncontrolled treatment-abroad cohorts and an open-label TBI study; no controlled trial, and a real risk of fatal cardiac arrhythmia. | Medium | Low | Low |
| 5-MeO-DMT Used alongside ibogaine in the Special Operations veterans-abroad cohorts; no controlled veteran data on its own. | Small | Very Low | Low |
MDMA and Veterans
MDMA is the most-studied psychedelic in veterans and the source of both the strongest controlled signal and the field’s biggest cautionary tale. In a randomised Phase 2 dose-response trial in 26 veterans, firefighters and police, the 75 mg group showed a large reduction in PTSD symptoms (Cohen’s d 2.8)[1] versus an active control, and a pooled analysis of six Phase 2 trials[2] found durable benefit, with the share no longer meeting PTSD criteria rising from 56% to 67% by one year.
But this is not a settled, approved treatment. In August 2024 the FDA declined to approve MDMA-assisted therapy for PTSD[3], issuing a Complete Response Letter and asking for another Phase 3 study, against a backdrop of concerns about functional unblinding (participants can tell whether they received MDMA) and trial conduct. The honest read is large but contested effects, not proof.
Ketamine and Veterans
Ketamine is the most-used and most-studied compound in veteran mental-health care, and the picture is genuinely mixed. For depression it is the strongest performer: a Bayesian dose-finding RCT in veterans with late-life treatment-resistant depression[1] found a 0.5 mg/kg infusion gave 70% response at day 7, and repeated infusions help veterans with comorbid PTSD and depression, though relapse came within weeks (median 41 days)[2].
For PTSD specifically the evidence is weaker. The largest controlled veteran trial, a multi-site RCT in 158 veterans and service members, was negative for PTSD[3], improving depression but not PTSD symptoms over placebo. Smaller open-label series in combat veterans report larger drops, but without a control group[4]. Esketamine is approved for treatment-resistant depression, not for PTSD.
Psilocybin and Veterans
Psilocybin in veterans is promising but early. A first-in-kind open-label pilot of a single 25 mg dose in 15 veterans with severe treatment-resistant depression[1] reported 60% response and 53% remission at three weeks. Crucially, the 12-month follow-up showed the benefit waned[2], with response falling from 80% at six months to 40% at twelve, which argues against any single-dose cure narrative.
Beyond depression, an uncontrolled psilocybin retreat in 21 veterans with a history of TBI[3] reported large drops in PTSD and depression scores. Veteran PTSD trials of psilocybin are mostly still in progress, and notably the acute psychedelic experience did not predict who improved, complicating simple "the trip heals you" accounts.
Ibogaine and Veterans
Ibogaine, often paired with 5-MeO-DMT, is the centre of the most distinctive veteran story in this field: Special Operations veterans travelling to clinics in Mexico because approved treatments failed them. A prospective study of 86 such veterans[1] and an earlier retrospective survey reporting very large before-after reductions in PTSD, depression and suicidal ideation[2] document real, self-reported relief, but the designs are uncontrolled, self-selected and self-funded, so the eye-popping effect sizes are hypothesis-generating, not proof.
The most rigorous ibogaine entry is the Stanford open-label study of magnesium-ibogaine in 30 veterans with traumatic brain injury[3], which reported large improvements in functioning, PTSD, depression and anxiety with no serious adverse events, the magnesium included specifically to reduce ibogaine’s risk of fatal cardiac arrhythmia. It remains single-arm, and its authors call for controlled trials.
Clinical Outlook
The near-term picture is a widening pipeline rather than a verdict. Veteran-focused trials now span a Phase 3 psilocybin study for treatment-resistant depression[1] due to start in 2026, several MDMA-assisted therapy trials (including group and massed-exposure formats), ketamine studies, and the magnesium-ibogaine line for TBI. The Department of Veterans Affairs has moved from caution toward funding and hosting psychedelic research, a significant shift for the field.
What real progress requires is clear from the same evidence: adequately controlled trials in veterans, and, for MDMA specifically, the additional study the FDA requested when it declined approval in 2024[2]. The honest counterweight to the optimism is attrition: several MDMA-in-veterans trials have been terminated or withdrawn, and the strongest controlled ketamine PTSD result was negative. The unmet need is real and the early signals are encouraging, but the proof is not yet in.
Industrial Landscape
The actors here are an unusual mix of public, non-profit, academic and grassroots. The Department of Veterans Affairs and the Department of Defense increasingly fund and run trials; Lykos Therapeutics (formerly the MAPS Public Benefit Corporation) led the MDMA programme; and academic centres, notably the Stanford group behind the magnesium-ibogaine work, drive much of the rigorous science. Veteran-led advocacy and philanthropic groups have funded research and lobbied for access.
Alongside the formal system sits an informal one: overseas clinics in Mexico and elsewhere that treat veterans with ibogaine and 5-MeO-DMT outside the regulated pipeline. That parallel economy is part of the honest picture, evidence of how far some veterans will go for relief, and a reminder that demand has run well ahead of regulated proof.
Quick Indicators
Organisations
Search →Ohio State University
The Ohio State University is a public land-grant research university based in Columbus, Ohio, offering undergraduate, graduate, and professional programs and conducting research across many fields. It was founded as the Ohio Agricultural and Mechanical College and serves as a major educational and economic institution in Ohio.
Resilient Pharmaceuticals
Resilient Pharmaceuticals (formerly Lykos Therapeutics, formerly MAPS PBC) is a US-based public benefit corporation developing MDMA-assisted therapy for PTSD. It was founded in 2014 by MAPS as a commercial spinout to carry MAPS MDMA research through late-stage trials and regulatory approval. After two Phase 3 trials and an NDA filing, FDA issued a Complete Response Letter in August 2024 and requested an additional Phase 3 trial before approval. The company subsequently restructured and rebranded, while the public Lykos web presence continues to describe the organisation as pursuing FDA approval for MDMA-assisted therapy. As of the June 2026 review, no public company announcement of a new pivotal trial start or NDA resubmission date was found. VA/DoD-backed MDMA/PTSD research is proceeding in the broader field, but it should not be treated as direct support for Resilient/Lykos NDA resubmission unless linked by company or FDA evidence.
MAPS
MAPS, the Multidisciplinary Association for Psychedelic Studies, is a U.S.-based 501(c)(3) nonprofit research and educational organization founded in 1986. It works nationally and with a broader global audience to develop medical, legal, and cultural contexts for the careful use of psychedelics and marijuana. Its core activities include research, education, advocacy, and convening the field through large public events. In psychedelic medicine and policy, MAPS positions itself as an advocate for legal access, drug policy reform, harm reduction, and health equity. Its Policy & Advocacy work includes legislative advocacy, community organizing, and impact litigation, and it has also launched work on access for system-impacted people and broader health equity in the legal psychedelic ecosystem. Current documented initiatives include the Psychedelic Science conference series, the Health Equity Program, The Zendo Project, and Ask MAPS, which handles public inquiries about therapy, research, and policy reform.
Ketamine Research Institute
The Ketamine Research Institute is a US-based clinical research organization developing precision medicine approaches to ketamine infusion therapy, studying optimized dosing protocols to treat depression and offering clinician training in evidence-based ketamine practice.
Usona Institute
Usona Institute is a US-based 501(c)(3) non-profit medical research organisation headquartered in Madison, Wisconsin. Usona develops and supports clinical research on psilocybin and other consciousness-expanding medicines with a mission-driven access model. Its psilocybin programme received FDA Breakthrough Therapy Designation for major depressive disorder in 2019. After completing the Phase 2 PSIL201 study, Usona launched the Phase 3 uAspire trial in 2024, a 240-participant randomised, double-blind multicentre study of 25 mg psilocybin with psychosocial support for adults with MDD. In April 2026, industry reporting said Usona confirmed it had received an FDA Commissioner National Priority Voucher for psilocybin in MDD, potentially shortening review if an NDA is filed and accepted. Usona is also exploring 5-MeO-DMT in early-stage research.
University of Minnesota
The Nielson Lab at the University of Minnesota is dedicated to understanding and treating trauma. More recently, the team here has been diving into psychedelic neuroscience research and drug policy reform thanks to funding from the newly created Psychedelic-Assisted THerapy (PATH) Fund at the UMN Foundation. The lab has been collecting survey data to assess the benefits and risks of ayahuasca use in naturalistic settings to treat symptoms of trauma. Additionally, Dr Jessica Nielson and her team are researching the neurological mechanisms of altered states of consciousness and their role in promoting neuroplasticity and wellness in healthy research participants.
Johns Hopkins University
The Centre for Psychedelic and Consciousness Research focuses on how psychedelics affect behavior, cognition, brain function, and biological health markers. They have been at the forefront of demonstrating the safety and efficacy of psychedelics for mental disorders, expanding their focus into psilocybin research across multiple mental health conditions, including smoking cessation, major depressive disorder, and cancer-related anxiety.
Stanford University
At the Stanford School of Medicine, researchers from the Rodriguez Lab and the Heifets Lab have united under the banner of the Stanford Psychedelic Science Group. Their primary clinical focus is to investigate compounds including ketamine, psilocybin, and MDMA as potential treatments for debilitating disorders such as obsessive-compulsive disorder (OCD), treatment-resistant depression, and post-traumatic stress disorder (PTSD).
Oregon Health & Science University
Researchers at the Social Neuroscience and Psychotherapy (SNAP) Lab at OHSU are investigating the therapeutic potential of psychedelics. Assistant Professor of Psychiatry, Dr Chris Stauffer, is the current director of the lab. SNAP Lab aims to maximize the benefits of therapeutic alliance and psychotherapy through the adjunct use of social psychopharmacology, such as oxytocin, MDMA, and psilocybin. Dr Stauffer led a research team from OHSU in a clinical trial exploring the effects of psilocybin in methamphetamine use disorder. With Oregon becoming the first state to legalize psilocybin-assisted therapy, more research is taking place at OHSU.
Washington University School of Medicine in St. Louis
The Program in Psychedelic Research (PiPer) is a partnership between The Healthy Mind Lab, the Washington University Neuroimaging Lab, and Usona Institute. PiPer leverages 30 years of neuroimaging research and four decades of psychiatry research. The group has started with four research projects around neuroimaging data in humans and animals. The university also serves as a site for Usona's Phase II/III trial with 25mg of psilocybin.
AIM Youth Mental Health
AIM Youth Mental Health is a US non-profit foundation founded in 2014 that funds scientific research and youth-led participatory action research to improve mental health outcomes for young people. The organization funds psilocybin research—including a study on how psilocybin affects genetic aging markers in young adults with stress-related disorders—alongside fellowships for postdoctoral youth mental health innovators.
Baylor College of Medicine
Academic medical center in Houston affiliated with multiple Texas Medical Center hospitals. Conducts psilocybin and MDMA clinical trials for veteran PTSD in partnership with the Michael E. DeBakey VA, and houses the ELIPSIS program — a dedicated initiative on the ethical and legal implications of psychedelics in society.
People
Search →Eduardo Schenberg
Neuroscientist and founder/director of Instituto Phaneros
A leading Brazilian psychedelic researcher known for clinical and translational work on ayahuasca, ibogaine, MDMA, and ethics/policy in psychedelic medicine.
Anna Forsyth
Doctoral researcher / researcher at the University of Auckland
She is an author on multiple clinical studies of LSD microdosing in depression and related psychedelic psychiatry work, contributing to early human evidence on efficacy, tolerability, and mechanism.
Neşe Devenot
Senior Lecturer in the University Writing Program at Johns Hopkins University
Neşe Devenot is a notable critic and scholar of psychedelic medicine whose work examines ethics, public discourse, and the social meanings of psychedelic-assisted therapy.
Jessica Maples-Keller
Associate Professor in the Emory School of Medicine, Department of Psychiatry and Behavioral Sciences; Associate Director of the Emory Healthcare Veterans Program
She is a prominent translational PTSD and psychedelic-therapy researcher contributing to MDMA and psilocybin studies, including work on fear extinction, treatment barriers, and culturally informed psychedelic-assisted therapy.
Michael Mithoefer
Senior Medical Director for Medical Affairs at MAPS PBC
Conducted the first FDA-approved clinical trial of MDMA-assisted therapy for PTSD.
Alan Davis
Associate Professor of Social Work & Director, Center for Psychedelic Drug Research
Noted for advancing epidemiological, naturalistic and mixed-method research on therapeutic and adverse outcomes of psychedelics and for translating those findings into clinical and harm-reduction contexts.
Brandon Weiss
Assistant Professor of Psychiatry and Behavioral Sciences
Noted for empirical work on personality change and contextual moderators in psychedelic-assisted interventions and for contributions to safety and phenomenology research across ayahuasca and psilocybin studies.
Amy Emerson
CEO of MAPS Public Benefit Corporation (MAPS PBC) / former Director of Clinical Research at MAPS
Notable for her contributions to multi-centre clinical research on MDMA-assisted psychotherapy for PTSD, including dose‑response, neuroimaging, long‑term follow-up and phase‑3 trial design.
Nathan Sepeda
Director of Data & Analytics
Notable for his contributions to clinical and experimental studies of psilocybin-assisted interventions, including trials of major depressive disorder and investigations of enduring psychological and neurofunctional effects.
Gonzalo Ona
Clinical Researcher in Psychedelic Psychopharmacology
Notable for epidemiological and clinical research on ayahuasca use, safety and wellbeing outcomes, and exploratory pharmacological work on 5‑MeO‑DMT and psychedelic interactions.
Benjamin Kelmendi
Clinical Researcher
Kelmendi is an active contributor to contemporary clinical and preclinical investigations of novel entactogens and psychedelic-assisted approaches, with work spanning pharmacology, addiction treatment strategies and clinician attitudes toward psychedelic therapies.
Robin Carhart-Harris
Ralph Metzner Distinguished Professor
Pioneering researcher in brain imaging of psychedelics and founding director of the UCSF Neuroscape Psychedelics Division.
Connected Evidence
The latest clinical data and verified academic findings associated with Veterans.