Toward a framework for psychedelic clinical trials in adolescents
Christine K. Moore, Henry Riordan, Rolana Avrumson, Philippe Auby
Child and Adolescent Psychiatry and Mental Health March 10, 2026 Peer reviewed DOI: 10.1186/s13034-026-01064-x via OpenAlex
Summary
Psychedelics show promise for treating mental health conditions in adults, leading to interest in their use among adolescents. Regulatory agencies may require trials for this younger population once adult therapies are approved. The paper outlines key considerations for designing and conducting these trials, emphasizing the need for enhanced psychological support and oversight to ensure safety and ethical standards in research involving adolescents.
Study at a glance
| Population | adolescents with mental health conditions |
|---|---|
| Key finding | The paper provides a framework for safely and ethically conducting clinical trials of psychedelic therapies in adolescents. |
Abstract
Recent clinical trials conducted by both industry and academic institutions have demonstrated the therapeutic potential of psychedelics for a variety of mental health conditions in adults. Considering the neurodevelopmental aspects of many of these disorders and the widespread occurrence of these conditions among younger individuals, there is increasing interest in exploring the potential for psychedelic therapies in the adolescent population. Regulatory agencies globally are also expected to require clinical trials in younger populations once such products are approved for adults. This paper details some key considerations for the design and conduct of such trials along with safeguards and best practices tailored to adolescents, building upon established methodologies from adult trials and emphasizing the importance of increased psychological support and rigorous trial oversight. Our goal is to provide a framework that ensures that future clinical trials involving the adolescent population are performed safely, ethically, and in accordance with the highest scientific and regulatory requirements, and to foster a patient-centric dialog within the regulatory and scientific community.