This Phase I open-label trial (n=14) studied the safety of psilocybin when administered to healthy participants enrolled in a psychedelic-assisted therapy training program. Participants ingested 25 mg of psilocybin extract, and vital signs, including heart rate, blood pressure, temperature, and ECG, were monitored throughout the study.
Adverse events were recorded at 2 days, 7 days, and 8 weeks following the psilocybin session. The trial aimed to collect physiological data and adverse events to help develop clinical screening protocols for psilocybin-assisted therapy, as well as assess the subjective effects of psilocybin at a dose of 25 mg.
Trial Details
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Sponsors & Collaborators
ATMA Journey CentersATMA Journey Centers was Canada’s first private therapy company to conduct legal psychedelic-assisted therapy using psilocybin.