|
Safety, feasibility, and preliminary clinical outcomes of psilocybin-assisted therapy for veterans with severe, treatment-resistant PTSD: an open-label pilot clinical trial.
2026
|
open-label pilot trial |
12 |
↑Supports
|
Psilocybin-assisted therapy was safe and well tolerated, with clinician-rated PTSD symptoms falling by a mean of 27.5 points from baseline to one-month follow-up and 75% achieving treatment response and remission. |
|
Study protocol of an open-label proof-of-concept trial examining the safety and clinical efficacy of psilocybin-assisted therapy for veterans with PTSD
2023
|
open-label pilot study protocol |
15 |
?Unclear
|
Describes a planned open-label trial of two psilocybin sessions (15 mg and 25 mg) with psychotherapy, with safety and CAPS-5 outcomes at one month and follow-up to six months. |
|
Investigational psilocybin treatment for post-traumatic stress disorder: a qualitative study of participant experience, trauma engagement, and differences from standard treatment.
2025
|
qualitative study nested in open-label phase 2 trial |
21 |
↑Supports
|
Participants described indirect engagement with trauma-related material through affective, somatic, and self-transcendent experiences, contrasting with standard treatments requiring direct confrontation with trauma memories. |
|
Silence is golden: Documenting the speech production of participants and support providers in psilocybin administration sessions for the treatment of post-traumatic stress disorder
2026
|
RCT (session-process analysis) |
22 |
?Unclear
|
During 25 mg COMP360 administration sessions, 78% of time was silence and support was minimally enacted yet experientially salient; no efficacy outcomes are reported. |
|
Psilocybin for PTSD with or without Psychotherapy: A Pilot study of safety and efficacy outcomes – The first characterization of nightmare burden in PTSD following psilocybin administration
2026
|
open-label controlled pilot trial |
18 |
?Unclear
|
Reports the design and dosing schedule (25 mg, optional 35 mg second session) of a nightmare-focused analysis but presents no nightmare-related results. |
|
Psilocybin Facilitates Fear Extinction: Importance of Dose, Context, and Serotonin Receptors
2024
|
experimental study (rodents) |
|
↑Supports
|
Psilocybin enhanced fear extinction, elevated extinction retention, and suppressed fear renewal, with effects dependent on dose, timing, concurrent extinction experience, and 5-HT2A receptors. |
|
Psilocybe cubensis extract potently prevents fear memory recall and freezing behavior in short- but not long-term in a rat model of posttraumatic stress disorder.
2024
|
preclinical study |
|
↕Mixed
|
Psilocybe cubensis extract (25 mg/kg) reduced PTSD-like freezing in the short term but not long term, while increasing pain threshold and decreasing anxiety. |
|
Efficacy of Psychoactive Drugs for the Treatment of Posttraumatic Stress Disorder: A Systematic Review of MDMA, Ketamine, LSD and Psilocybin
2020
|
systematic review |
9 |
?Unclear
|
Nine trials met criteria (five ketamine, four MDMA); no psilocybin or LSD trials were identified, and MDMA plus psychotherapy had moderate-quality evidence while ketamine evidence was low to very low. |
|
A Systematic Review of the efficacy, safety, and Tolerability of Psychedelics in the Treatment of post-traumatic Stress Disorder
2025
|
systematic review |
42 |
↕Mixed
|
Ketamine and MDMA had the most developed evidence for PTSD, while data for psilocybin, ayahuasca, DMT, LSD, and ibogaine were preliminary but suggested potential benefits. |
|
Efficacy and risks of psychedelics in treatment of posttraumatic stress disorder: A systematic review
2026
|
systematic review |
|
?Unclear
|
MDMA and IV ketamine currently have the greatest support for efficacy in PTSD, and randomized controlled studies of psilocybin and LSD are still needed. |
|
The Psychedelic Future of Post-Traumatic Stress Disorder Treatment
2024
|
comprehensive review |
|
↑Supports
|
Initial clinical trials demonstrate potential value of psychedelic-assisted therapy for PTSD, including psilocybin, while standard-of-care therapies leave many patients symptomatic. |
|
Diverse therapeutic developments for post-traumatic stress disorder (PTSD) indicate common mechanisms of memory modulation.
2022
|
review |
|
↑Supports
|
Early evidence supports beneficial effects of psychedelics, including psilocybin, particularly with psychotherapy, potentially by reducing barriers to therapy and modulating fear memory, but large-scale trials are needed. |
|
Mechanisms of psilocybin on the treatment of posttraumatic stress disorder
2024
|
review |
|
↑Supports
|
Argues that psilocybin may be an underexplored treatment option for PTSD based on its pharmacology and psychoanalytic principles, though further research is required. |
|
Psychoactive Drugs in the Management of Post Traumatic Stress Disorder: A Promising New Horizon
2022
|
review |
|
↑Supports
|
Describes MDMA, ketamine, and psilocybin as targeting fear and anxiety pathways and holding potential for refractory or treatment-resistant PTSD. |
|
Psychedelic Therapies in the Management of Post-Traumatic Stress Disorder
2026
|
review |
|
↑Supports
|
Psychedelics induce neuroplasticity and augment fear extinction; MDMA-assisted therapy showed high efficacy, and psilocybin effectively treats common comorbidities such as anxiety and treatment-resistant depression. |
|
[The use of psychedelics in psychiatry].
2026
|
review |
|
↕Mixed
|
Argues that psilocybin shows consistent improvements in depression and that MDMA-assisted psychotherapy has the largest phase 3 PTSD dataset (though FDA declined approval in 2024), while certainty of evidence remains low or very low and psychedelics should be considered experimental. |
|
Novel psychopharmacological therapies for psychiatric disorders: psilocybin and MDMA.
2016
|
review |
|
↕Mixed
|
Psilocybin is being tested for alcoholism, smoking cessation, and cancer-related anxiety, while MDMA shows encouraging results for refractory PTSD; both are studied as adjuncts to psychotherapy. |
|
Registered clinical studies investigating psychedelic drugs for psychiatric disorders.
2021
|
review of registered trials |
70 |
?Unclear
|
As of December 2020, 70 registered trials studied psychedelics for psychiatric disorders, mostly MDMA and psilocybin for PTSD and major depression, with only 21 having published results. |
|
A Systematic Review of the Neurocognitive Effects of Psychedelics in Healthy Populations: Implications for Depressive Disorders and Post-Traumatic Stress Disorder
2024
|
systematic review |
43 |
↕Mixed
|
Most studies in healthy subjects reported detrimental or neutral effects on cold cognition during peak psychedelic effects, with few exceptions; only one article addressed cognition in PTSD (MDMA). |
|
Theorizing that Psychedelic Assisted Therapy May Play a Role in the Treatment of Trauma-Induced Personality Disorders.
2024
|
theoretical paper |
|
↑Supports
|
Argues that BPD be reframed as traumatic personality stress disorder and that psychedelic-assisted therapy may be a pathway for treating both BPD and PTSD. |
|
SSRIs, Psilocybin, MDMA, and Disease Modeling: Strategies to Advance PTSD Treatment
2026
|
position paper |
|
?Unclear
|
Argues that SSRIs, psilocybin, and MDMA act on serotonergic circuits and are used or proposed for PTSD, but their molecular, cellular, and circuit mechanisms remain poorly understood. |
|
Psychedelics as a Therapeutic Opportunity or Threat: A Narrative Review.
2025
|
narrative review |
|
↑Supports
|
Psilocybin and MDMA show therapeutic potential for depression, alcohol use disorders, and PTSD, but require careful patient selection and further research given risks of adverse reactions and drug interactions. |
|
Is it now time to prepare psychiatry for a psychedelic future?
2024
|
review/commentary |
|
?Unclear
|
Explores opportunities and challenges for psychiatry after Australia rescheduled psilocybin and MDMA as treatments for treatment-resistant depression and PTSD respectively. |
|
Australia’s approval of MDMA and psilocybin for PTSD and depression is premature, say critics
2023
|
news report |
|
?Unclear
|
Reports that Australia's TGA attached conditions to MDMA and psilocybin use, including authorized psychiatrists, ethics committee approval per patient, and use with psychotherapy. |
|
Australia to prescribe MDMA and psilocybin for PTSD and depression in world first
2023
|
news report |
|
↓Opposes
|
Reports that Australia's decision to make MDMA and psilocybin available for PTSD and depression was dogged by suggestions that it was rushed. |