Trump announces reforms to accelerate access to psychedelic drug treatments
The order opens a pathway for seriously ill patients to access investigational psychedelics and keeps ibogaine scheduled while federal agencies speed review.
- On Saturday, President Donald Trump signed an executive order directing the U.S. Food and Drug Administration to fast-track reviews of breakthrough-designated psychedelic therapies and allocated $50 million in federal funding for private-sector research.
- The order responds to the mental health crisis affecting veterans, with Trump citing the "life-changing potential" of experimental treatments, following Health and Human Services Secretary Robert F. Kennedy Jr.'s criticism of the FDA's "aggressive suppression of psychedelics."
- Shares of Atai Life Sciences and Compass Pathways surged Monday as the order introduces "National Priority Vouchers," potentially cutting FDA review timelines for breakthrough-designated drugs to one or two months from six to 10 months.
- Oppenheimer analyst Jay Olson called the move a "structural inflection" that reduces development risk, while Jefferies analyst Andrew Tsai described it as an "official stamp of validation" signaling government support is "real" and "actionable."
- While the order focuses on ibogaine research, the drug remains a Schedule I substance linked to "cardiovascular toxicity." FDA Commissioner Marty Makary indicated decisions on priority vouchers could arrive this summer, with analysts monitoring potential approvals between 2027 and 2030.
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380 Articles
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On Saturday, April 18, President Trump issued an executive order relating to the development of psychedelic substances as medicine. This represents a remarkable moment in the arc of post-1970’s drug policy: We have a Republican administration formally directing federal agencies to accelerate access to psychedelic drugs—including ibogaine, psilocybin, and LSD—as potential treatments for serious mental illnesses like major depressive disorder and …
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