26 September 2025
Crunching the Numbers on Psychedelic Therapies:
Cost, Coverage, and Access
By: Elliot Marseille, DrPH, MPP; Director, Collaborative for the Economics of Psychedelics, UC Berkeley
MAPS Bulletin: Volume XXXIV

The psychedelic resurgence has reached a critical juncture. While clinical trials demonstrate remarkable efficacy for MDMA and psilocybin-assisted therapies, among others, in treating conditions like PTSD and major depression, a fundamental question remains: Can these treatments become accessible to the millions who need them? The answer lies not just in regulatory approval, but in the economics that will determine whether insurers cover these therapies and healthcare systems adopt them at scale.
The Economic Imperative
Mental health disorders represent the fifth leading cause of disability-adjusted life years globally, affecting over 10.7% of the world’s population1. Depression represents about a third of this burden, as do anxiety disorders and post-traumatic stress disorder (PTSD), followed by alcohol and drug use disorders at 13.1 and 8.4%, respectively. The remaining 10% consists of bipolar disorder, schizophrenia, and eating disorders. In the United States 21.0% of adults live with mental illness, including 5.6% with serious mental health conditions2. PTSD affects over 12 million Americans, generating billions in direct medical costs and lost productivity annually3. Traditional treatments often fall short—nearly half of PTSD patients show no significant improvement with existing therapies, and dropout rates remain stubbornly high.
Against this backdrop of unmet need, psychedelic-assisted therapies offer transformative potential. Recent Phase 3 trials showed that 67% of patients receiving MDMA-assisted therapy no longer met PTSD criteria after treatment, compared to just 32% in the placebo group4. Yet without robust economic analysis, even the most effective treatments can languish in academic journals rather than reaching clinical practice.
This is where health economics becomes essential. Payers—whether government programs like Medicare and Medicaid, commercial insurers, or health systems in other countries—make coverage decisions based on value, not just efficacy. They need to know: What does it cost? How does it compare to existing treatments? What’s the return on investment in terms of both health outcomes and dollars saved?
Lessons from Ukraine: A Test Case for Global Implementation
The ongoing conflict in Ukraine presents both a humanitarian crisis and an unprecedented opportunity to demonstrate the scalability and cost-effectiveness of psychedelic therapies. Our recent analysis at the Collaborative for the Economics of Psychedelics estimated that 6.4 million Ukrainians now suffer from severe PTSD—a staggering burden for a nation already stretched thin by war.
Our modeling suggests that MDMA-assisted therapy, adapted for the Ukrainian context with group therapy components to maximize efficiency, could save tens of thousands of lives while generating substantial economic benefits. Treating just 1,000 patients would cost approximately $1.1 million but would prevent 20 deaths and yield 717 quality-adjusted life years (QALYs)—a metric that captures both length and quality of life. If Ukraine could treat half of all PTSD patients over a decade, the intervention could save 48,000 lives while generating $5.6 billion in societal savings through reduced healthcare costs and improved productivity5.
Crucially, the Ukrainian model demonstrates how psychedelic therapies might be adapted for resource-constrained settings. Rather than the intensive two-therapist model typically used in U.S. trials, group therapy protocols could reduce per-patient costs while maintaining efficacy. This has profound implications not just for Ukraine, but for low- and middle-income countries worldwide where mental health resources are scarce but trauma is abundant. This applies to the United States too, where the scarcity of appropriately trained clinicians would be a major bottleneck limiting access.
The Ukrainian government has already begun laying groundwork, with the Multidisciplinary Association for Psychedelic Studies training nearly 60 Ukrainian therapists in MDMA protocols this past spring. This represents more than humanitarian aid—it’s a real-world laboratory for understanding how psychedelic therapies can be implemented at population scale under challenging conditions.
Our modeling suggests that MDMA-assisted therapy, adapted for the Ukrainian context with group therapy components to maximize efficiency, could save tens of thousands of lives while generating substantial economic benefits.
The U.S. Payer Perspective: From Cost to Value
In the United States, our economic analyses paint an encouraging picture for payer adoption. Using data from Phase 3 trials, we found that MDMA-assisted therapy for severe PTSD is not just cost-effective but potentially cost-saving from a payer’s perspective. Over a 10-year horizon, the therapy could save the healthcare system approximately $47,000 per patient while delivering 2.1 additional QALYs —a remarkable return on investment by any standard6.
The key drivers of these savings are reduced emergency department visits, fewer hospitalizations, decreased need for ongoing psychiatric care, and lower rates of treatment for other comorbid conditions. When patients achieve remission from PTSD, the benefits ripple through the healthcare system. From the broader perspective of society at large, benefits are even greater since our analysis didn’t account for other effects such as increased productivity as people are able to return to work.
For commercial insurers and state Medicaid programs, the calculus involves balancing upfront costs against long-term savings. At an estimated $11,000-$15,000 per treatment course, MDMA-assisted therapy requires significant initial investment. Yet when compared to the lifetime costs of untreated severe PTSD—often exceeding $500,000 per patient—the economic case becomes compelling.
The Critical Need for Real-World Evidence
As we move from clinical trials to clinical practice, the need for standardized, real-world data collection becomes paramount. The controlled environment of trials, with carefully selected patients and highly trained therapists, may not reflect the messiness of actual healthcare delivery. We need to know: How well do these therapies work in community settings? What’s the optimal therapist training protocol? How do outcomes vary across different populations and settings?
This is why establishing uniform data collection standards now, before widespread rollout, is crucial. Every patient treated represents an opportunity to refine our understanding of both clinical effectiveness and economic value. Key metrics should include not just symptom reduction but functional improvement, healthcare utilization, work productivity, and quality-of-life measures. The latter can include positive measures of flourishing beyond the mere reduction of symptoms.
The Collaborative for the Economics of Psychedelics has been working to develop these frameworks, drawing on decades of experience in global health economics. We’re advocating for registry systems that can track patients longitudinally, capturing both benefits and any adverse effects that emerge over time. This real-world evidence will be essential for securing broader payer coverage and optimizing treatment protocols.
Equity and Access: The Ultimate Goal
Perhaps the most important economic question is not whether psychedelic therapies are cost-effective, but how to ensure equitable access. Without deliberate planning, these treatments risk becoming boutique therapies for the affluent rather than transformative public health interventions.
Group therapy models, being explored both in the United States and abroad, offer one pathway to democratizing access7. Training programs that credential a diverse workforce of therapists—not just psychiatrists and psychologists but social workers, counselors, and peer support specialists—could help meet demand while controlling costs. Innovative payment models, such as outcomes-based contracts where manufacturers share risk with payers, might accelerate adoption.
The economics of psychedelics ultimately serve a larger purpose: turning scientific breakthroughs into accessible treatments for those who need them most. Whether it’s a veteran in rural America, a conflict survivor in Ukraine, or anyone struggling with treatment-resistant mental illness, the goal remains the same—ensuring that ability to pay doesn’t determine access to healing.
Frontiers of Psychedelic Therapy: An Expanding Economic Horizon
While MDMA for PTSD has captured headlines, it represents just the beginning of psychedelic medicine’s economic potential. Across the spectrum of mental health and behavioral disorders, emerging therapies show promise that could fundamentally reshape healthcare economics.
Consider ibogaine for opioid use disorder. Early studies suggest that a single ibogaine treatment could interrupt addiction patterns that typically require months of conventional medication-assisted treatment8. For traumatic brain injury, affecting millions of veterans and civilians, preliminary research indicates ibogaine might offer neuroprotective benefits where conventional treatments have failed9. The economic implications are staggering: if even partially effective, these interventions could save thousands of lives while reducing the enormous burden on emergency departments, criminal justice systems, and families.
Psilocybin-assisted therapy presents similarly compelling economics across multiple indications. For tobacco cessation, where traditional quit rates hover around 15-30%, early trials show success rates exceeding 80% at six months10,11. Given that smoking still kills more than 480,000 Americans annually and smoking costs the U.S. over $600 billion annually, even modest improvements in cessation rates could generate billions in savings12. Alcohol use disorder affects over 29.5 million Americans and costs society about $249 billion yearly13. Thus, psilocybin’s ability to reduce heavy drinking days and promote abstinence could transform both individual lives and public health budgets14. Our team at CEP is modeling these scenarios, and preliminary analyses suggest cost-effectiveness ratios that would make these treatments attractive to even the most conservative payers.
The therapeutic landscape extends further still. LSD for generalized anxiety disorder, affecting 6.8 million American adults, could offer relief where SSRIs and benzodiazepines often fall short. DMT for treatment-resistant depression—a condition affecting millions who have exhausted conventional options—might provide rapid relief similar to ketamine but with potentially longer-lasting effects. Each of these indications represents not just clinical opportunity but economic necessity. The cumulative burden of mental health and substance use disorders exceeds $1 trillion annually in the United States alone when accounting for healthcare costs, lost productivity, and premature mortality.
What makes these therapies particularly compelling from an economic standpoint is their potential for durable responses after limited treatment courses. Unlike traditional psychiatric medications requiring daily dosing for years or decades, psychedelic-assisted therapies typically involve just a few sessions. This fundamental difference in treatment architecture could revolutionize mental healthcare economics—shifting from chronic disease management to potential long-term remission or (dare we say it?), cure.
Of course, the evidence base varies considerably across these applications. While MDMA for PTSD and psilocybin for depression have advanced to Phase 3 trials, other indications remain in earlier stages of investigation. Yet the consistency of positive signals across diverse conditions and compounds suggests we’re observing a genuine therapeutic class effect rather than isolated successes. For health economists, this presents both opportunity and challenge: how to model the potential impact of therapies that might fundamentally alter disease trajectories in ways our current frameworks struggle to capture.
Perhaps the most important economic question is not whether psychedelic therapies are cost-effective, but how to ensure equitable access. Without deliberate planning, these treatments risk becoming boutique therapies for the affluent rather than transformative public health interventions.
The Path Forward
As the field advances, economic analysis will play an increasingly central role in shaping the psychedelic therapy landscape. The expanding pipeline of psychedelic therapies—from established compounds like MDMA and psilocybin to emerging treatments with ibogaine, LSD, and DMT—demands sophisticated economic modeling that can capture both immediate costs and long-term societal benefits. The work being done now—developing cost-effectiveness models, analyzing payer perspectives, designing equitable access frameworks—lays the foundation for a future where these treatments are not exotic experiments but standard care options.
The recent FDA setback for MDMA-assisted therapy, while disappointing, provides an opportunity to strengthen the economic evidence base. Additional trials, if designed with economic endpoints in mind, could address payer concerns while generating the real-world evidence needed for broad implementation.
The promise of psychedelic therapies extends beyond individual healing to societal transformation. By demonstrating their economic value—not just their clinical efficacy—we can build the case for the infrastructure, training, and coverage policies needed to realize this potential. The numbers tell a compelling story: these therapies can save lives, reduce suffering, and generate economic value. Our task now is to ensure that story reaches the decision-makers who hold the keys to access.
The emergence of psychedelic-assisted therapies represents a rare opportunity to fundamentally improve mental healthcare while potentially reducing its economic burden. Through rigorous economic analysis, thoughtful implementation strategies, and commitment to equity, we can help ensure these treatments fulfill their transformative promise—not just for some, but for all who need them.
References
- Mental Health. OurWorldInData.org; 2021. ‘https://ourworldindata.org/mental-health.
- Substance Abuse and Mental Health Services Administration. Results from the 2020 National Survey on Drug Use and Health: Detailed tables. Rockville, MD: Center for Behavioral Health Statistics and Quality;2021.
- Kessler RC, Chiu WT, Demler O, Merikangas KR, Walters EE. Prevalence, severity, and comorbidity of 12-month DSM-IV disorders in the National Comorbidity Survey Replication. Arch Gen Psychiatry. 2005;62(6):617–627.
- Mitchell JM, Bogenschutz M, Lilienstein A, et al. MDMA-assisted therapy for severe PTSD: a randomized, double-blind, placebo-controlled phase 3 study. Nature Medicine. 2021.
- Marseille E, Chernoloz O, Orlov O. The Potential Economic and Public Health Impact of MDMA-Assisted Group Therapy for PTSD in Ukraine. World Medical & Health Policy.n/a(n/a).
- Marseille E, Mitchell JM, Kahn JG. Updated cost-effectiveness of MDMA-assisted therapy for the treatment of posttraumatic stress disorder in the United States: Findings from a phase 3 trial. PLoS One. 2022;17(2):e0263252.
- Marseille E, Stauffer CS, Agrawal M, et al. Group psychedelic therapy: empirical estimates of cost-savings and improved access. Front Psychiatry. 2023;14:1293243.
- Mash DC, Duque L, Page B, Allen-Ferdinand K. Ibogaine Detoxification Transitions Opioid and Cocaine Abusers Between Dependence and Abstinence: Clinical Observations and Treatment Outcomes. Front Pharmacol. 2018;9:529.
- Cherian KN, Keynan JN, Anker L, et al. Magnesium-ibogaine therapy in veterans with traumatic brain injuries. Nat Med. 2024;30(2):373–381.
- Johnson MW, Garcia-Romeu A, Griffiths RR. Long-term follow-up of psilocybin-facilitated smoking cessation. Am J Drug Alcohol Abuse. 2017;43(1):55–60.
- Koegelenberg CF, Noor F, Bateman ED, et al. Efficacy of varenicline combined with nicotine replacement therapy vs varenicline alone for smoking cessation: a randomized clinical trial. JAMA. 2014;312(2):155–161.
- Office on Smoking and Health NCfCDPaHP, Centers for Disease Control and Prevention. Burden of Cigarette Use in the U.S. 2024.
- Choi HY, Balter DR, Haque LY. Epidemiology and Health Care Burden of Alcohol Use Disorder. Clin Liver Dis. 2024;28(4):577–588.
- Bogenschutz MP, Ross S, Bhatt S, et al. Percentage of Heavy Drinking Days Following Psilocybin-Assisted Psychotherapy vs Placebo in the Treatment of Adult Patients With Alcohol Use Disorder: A Randomized Clinical Trial. JAMA Psychiatry. 2022;79(10):953–962.
Elliot Marseille, DrPH, MPP
Dr. Elliot Marseille is Principal of the firm, Health Strategies International. He has 35 years of senior public health management and research experience and has published widely on the cost-effectiveness of a range of global health diseases and conditions, with a focus on HIV/AIDS. He is the Course Director for Cost-Effectiveness Analysis in Medicine and Public Health, at UCSF. Dr. Marseille is a leading expert on the economics of the emerging psychedelic-assisted therapies to treat a range of psychiatric indications. He consults with the Multidisciplinary Association for Psychedelic Studies (MAPS) in modeling the economics of MDMA-assisted psychotherapy for the treatment of severe, treatment-resistant PTSD; with the Usona Institute in analyzing the cost-effectiveness of psilocybin-assisted therapy to treat major depression; and with John Hopkins University on the cost-effectiveness of psilocybin-assisted therapy for tobacco cessation. Additional interests include understanding the ethical foundations of cost-effectiveness analysis and identifying sound criteria for judging cost effectiveness.

Become a MAPS Member with a monthly donation
As a Member, you’re not just making a donation — you’re joining a community that is at the forefront of advancing research, changing policy, and evolving education around psychedelics. Join us in shaping a future where these life-changing tools are available to those who need them most.

