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Evidence

What the clinical trials found.
Sources linked, limits stated.

I keep this index so you can read the studies yourself. Each entry says who was studied, what the trial found and what it did not show. It is for informed decision-making, not medical advice.

Written by Austin MaoLast updated: October 2026
Research artifacts illustrating Ceremonia's clinical-research index
This page provides educational information about clinical research. It does not constitute medical advice. Consult a qualified clinician before making any health decisions.

Curated studies

Depression2021 · New England Journal of Medicine · n=59

Trial of Psilocybin versus Escitalopram for Depression

On the primary outcome (QIDS-SR-16 at 6 weeks), two psilocybin doses and escitalopram did not differ significantly (-8.0 vs -6.0; p=0.17); the trial was not powered to show equivalence. Secondary outcomes, such as remission (57% vs 28%), favored psilocybin but were not corrected for multiple comparisons. The trial enrolled moderate-to-severe major depression, not treatment-resistant depression.

Read paper →
Depression2021 · JAMA Psychiatry · n=24

Effects of Psilocybin-Assisted Therapy on Major Depressive Disorder

In a waitlist-controlled, unblinded trial of 24 adults with major depressive disorder, 71% showed a clinically significant response at 4-week follow-up, with 54% meeting remission criteria. Participants were not required to be treatment-resistant.

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Anxiety2016 · Journal of Psychopharmacology · n=51

Psilocybin produces substantial and sustained decreases in depression and anxiety in patients with life-threatening cancer

In a randomized, double-blind crossover trial against a very low dose, about 80% of cancer patients still showed clinically significant reductions in depressed mood and anxiety at the 6-month follow-up after a high-dose session. Population: people with life-threatening cancer.

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Anxiety2016 · Journal of Psychopharmacology · n=29

Rapid and sustained symptom reduction following psilocybin treatment for anxiety and depression in patients with life-threatening cancer

In a randomized crossover trial of cancer patients, about 60 to 80% showed anti-anxiety and antidepressant response at 6.5 months. A within-subject follow-up of the cohort (Agin-Liebes et al., 2020; uncontrolled, 15 of 16 survivors) found 60 to 80% still met response criteria at 4.5 years.

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Addiction2022 · JAMA Psychiatry · n=95

Percentage of Heavy Drinking Days Following Psilocybin-Assisted Psychotherapy vs Placebo in the Treatment of Adult Patients With Alcohol Use Disorder

Heavy drinking days were 9.7% with psilocybin vs 23.6% with an active placebo (diphenhydramine) over 32 weeks; psychotherapy was given in both groups. Evidence is mixed: a smaller 2025 phase 2 trial after inpatient withdrawal (n=37 analysed) found no significant between-group difference in abstinence duration (Rieser et al.).

Read paper →
Depression2022 · New England Journal of Medicine · n=233

Single-Dose Psilocybin for a Treatment-Resistant Episode of Major Depression

At week 3, 25 mg reduced MADRS scores significantly more than 1 mg (-12.0 vs -5.4; difference -6.6, 95% CI -10.2 to -2.9). The 10 mg dose (-7.9) did not differ significantly from 1 mg (p=0.18). Adverse events occurred in 77% of participants, and suicidal ideation or behavior was seen in all dose groups.

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Addiction2026 · JAMA Network Open · n=82

Psilocybin or Nicotine Patch for Smoking Cessation: A Pilot Randomized Clinical Trial

At 6 months, 40.5% of the psilocybin group vs 10.0% of the nicotine-patch group had biochemically verified prolonged abstinence (OR 6.12; 95% CI 1.99-23.26), with CBT in both groups. A pilot in psychiatrically healthy smokers; not generalizable to complex comorbidity.

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Addiction2014 · Journal of Psychopharmacology · n=15

Pilot study of the 5-HT2AR agonist psilocybin in the treatment of tobacco addiction

In an open-label pilot with no control group, 12 of 15 participants (80%) had biochemically verified 7-day abstinence at 6 months; 60% at long-term follow-up (Johnson et al., 2017).

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Depression2019 · Psychological Medicine · n=29

Rapid antidepressant effects of the psychedelic ayahuasca in treatment-resistant depression: a randomized placebo-controlled trial

MADRS scores were lower with ayahuasca than placebo at days 1, 2 and 7 in treatment-resistant depression; day-7 response was 64% vs 27% (the difference in remission was a trend, p=0.054). It remains a single small randomized trial, and no large trial has been located.

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Depression2016 · The Lancet Psychiatry · n=12

Psilocybin with psychological support for treatment-resistant depression: an open-label feasibility study

An open-label study of 12 treatment-resistant patients found mean QIDS scores 11.8 points lower at 1 week and 9.2 points lower at 3 months. There was no placebo group.

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Mechanism2012 · Proceedings of the National Academy of Sciences

Neural correlates of the psychedelic state as determined by fMRI studies with psilocybin

An fMRI study in healthy volunteers: intravenous psilocybin decreased cerebral blood flow and BOLD signal in hub regions, including the medial prefrontal and posterior cingulate cortices, and reduced coupling between them. Increased between-network communication was reported in later work, such as Daws et al. (Nature Medicine, 2022).

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Mechanism2021 · Neuron

Psilocybin induces rapid and persistent growth of dendritic spines in frontal cortex in vivo

A mouse study: one psilocybin dose raised dendritic spine density and size in frontal cortex by about 10% within 24 hours, with effects lasting at least one month. A preclinical finding; human structural plasticity has not been measured directly.

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Microdosing2021 · eLife · n=191

Self-blinding citizen science to explore psychedelic microdosing

A self-blinding study of 191 microdosers. Microdose and placebo groups both improved with no significant difference between them; small acute differences were consistent with participants breaking blind.

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Microdosing2022 · Translational Psychiatry · n=34

Microdosing with psilocybin mushrooms: a double-blind placebo-controlled study

A double-blind study in 34 people starting to microdose. Noticeable subjective effects and altered EEG rhythms, but no evidence of enhanced well-being, creativity or cognition; the authors point to expectation.

Read paper →

Deep dives by condition

Psilocybin & AnxietyDeep dive →Psilocybin & DepressionDeep dive →Psilocybin & PTSDDeep dive →

Where the field stands

Psilocybin research began in the 1950s and 1960s with promising early results in addiction, depression, and end-of-life anxiety. Criminalization under the Controlled Substances Act in 1970 halted almost all clinical work for three decades. Research restarted in the 2000s, when Johns Hopkins University received US authorization for a psilocybin study (Griffiths et al., 2006) and Imperial College London began studies under UK regulation.

Since 2000, the field has accumulated peer-reviewed evidence across several conditions, much of it from small trials. As of October 2026, COMPASS Pathways has reported two phase 3 trials in treatment-resistant depression (sponsor-reported) and Usona Institute has completed enrollment in a phase 3 trial in major depressive disorder. No psilocybin product is FDA-approved.

FDA granted Breakthrough Therapy designation to COMPASS Pathways' psilocybin (COMP360) for treatment-resistant depression in October 2018 and to Usona Institute's psilocybin for major depressive disorder in November 2019. The designation is an expedited review pathway for those sponsors' products in development. It is not approval of psilocybin or of any setting.

Psilocybin is a naturally occurring indole alkaloid found in approximately 200 species of fungi worldwide. In the body it converts to psilocin, which acts as a partial agonist at serotonin 2A receptors (5-HT2A), particularly in the prefrontal cortex. Onset is typically 20 to 40 minutes after oral ingestion, with a peak at 90 to 120 minutes and a total duration of 4 to 6 hours.

Further reading

The Body Keeps the Score: Brain, Mind, and Body in the Healing of Trauma, van der Kolk, Bessel, Viking, 2014. A trade book that synthesizes trauma research and clinical practice. Read it as an introduction to the field, not as a study.

Want to read a study the way I do? How we read a study. Prefer the explainers? Start at the science hub.

Inclusion criteria

Studies included in this index are peer-reviewed, conducted as randomized controlled trials or open-label trials, have a sample size of at least 10 participants, and are published in an indexed journal. We review and update this index periodically as new research is published. The few mouse, imaging and microdosing entries are labeled by condition so you can tell them apart.

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