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SB 1767

SB 1767 - Under this act, any person who acquires, uses, produces, possesses, transfers, or administers psilocybin for the person's own therapeutic use shall not be subject to state or local criminal or civil penalties if the person is a veteran or first responder and is 21 years of age or older and suffers from a condition listed in the act. The person shall be enrolled in a study regarding the use of psilocybin to treat such conditions and shall provide the Department of Mental Health with specified information. A facilitator shall be present during the administration of the psilocybin and the use of psilocybin shall be limited to no more than 150 milligrams of psilocybin analyte during any 12-month period. A person who assists another in any of the acts permitted under this act and any laboratory testing psilocybin under this act shall not be subject to state or local criminal or civil penalties. Subject to appropriation, the Department shall provide grants totaling $2 million dollars for research on the use and efficacy of psilocybin for the treatment of conditions listed in the act. The Department shall prepare annual reports for the Governor, Lieutenant Governor, and the General Assembly on the implementation and outcomes of psilocybin use under this act. No state agency shall disclose to the federal government or any unauthorized third party the statewide list or any individual information of persons who meet the requirements of this act. Additionally, this act modifies current law on the use of investigational drugs and devices for individuals with terminal illnesses to include individuals with life-threatening or severely debilitating conditions or illnesses. Currently, investigational drugs shall not include Schedule I controlled substances. This act repeals that prohibition. This provision is substantially similar to SB 1454 (2026). Finally, this act requires the Department of Mental Health, in collaboration with a Missouri university hospital or contract research organizations conducting FDA-approved trials, to conduct a study on the efficacy of using alternative medicine and therapies, including, but not limited to, the use of psilocybin, for the treatment of veterans and first responders suffering post-traumatic stress disorder, major depressive disorder, substance use disorders, or who require end-of-life care, as described in the act. Such study shall include a study of the use of psilocybin to treat such conditions, as well as a literature review and the submission of various reports. No person participating in the study shall be subject to criminal or civil liability or sanction for participating, except in cases of gross negligence or willful misconduct. This act is identical to SB 1682 (2026), substantially similar to HB 1717 (2026), and similar to SCS/SB 90 (2025), SCS/SB 768 (2024), HCS/HB 1830 (2024), HB 1154 (2023), and SB 614 (2023). SARAH HASKINS

2026 Regular Session Introduced by Rick Brattin

Missouri bill modifies regulations to permit psilocybin use as alternative therapeutic treatment, creating state-level medical access despite federal Schedule I classification.

Second Read and Referred S Emerging Issues and Professional Registration Committee
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Bill Summary · SB 1767

Legislative bill overview

SB 1767 modifies Missouri's legal framework governing alternative therapies and treatments, with specific provisions addressing psilocybin (the active compound in certain mushrooms). The bill appears to create regulatory pathways or licensing mechanisms for psilocybin-related therapeutic use. This represents a shift toward medical access in a state that currently classifies psilocybin as a Schedule I controlled substance.

Why is this important

Psilocybin has shown clinical promise in treating treatment-resistant depression, PTSD, and end-of-life anxiety in peer-reviewed research, yet remains federally illegal. States like Oregon and Colorado have begun establishing regulated psilocybin programs, creating a national policy divergence. Missouri's approach could affect patient access to experimental treatments, establish regulatory precedent in a conservative state, and potentially influence how other states balance federal law with emerging medical evidence.

Potential points of contention

  • Federal-state conflict: Psilocybin remains a Schedule I drug under the Controlled Substances Act, creating legal tension between state authorization and federal prohibition
  • Scope of "alternative therapies": Unclear whether the bill broadly permits various alternative treatments beyond psilocybin or maintains restrictions, and what "alternative" encompasses
  • Patient access and equity: Questions about who qualifies for treatment, affordability, potential disparities in access, and whether recreational use could be inadvertently enabled

Compiled from official sources — confirm details with the bill’s official record.

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