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In this video series segment, Casey Paleos, MD, offers insight into the impact of historic stigma associated with psychedelic therapies on acceptance in psychiatric care.
As the calendar turns from July to August, the psychiatry community’s gaze now finds itself affixed to August 11 and the US Food and Drug Administration’s decision surrounding Lykos Therapeutics’ application for 3,4-methylenedioxymethamphetamine (MDMA)-assisted therapy for the treatment of posttraumatic stress disorder (PTSD).
Despite backing from a pair of phase 3 randomized, double-blind, placebo-controlled trials in MAPP1 and MAPP2, MDMA-assisted therapy has encountered numerous hurdles on the way to this potential decision, including the historic stigma attached to use of MDMA as a result of its Schedule 1 controlled substance and, more recently, a negative outcome from a meeting convened by the FDA’s Psychopharmacologic Drugs Advisory Committee in early June.
As part of our ongoing coverage leading up to this historic FDA decision, we contacted leading subject matters in the field. In this video series, our audience can hear the perspective of Casey Paleos, MD, an adult psychiatrist in a New York-based private practice and the Chief Medical Officer of InnerMost PBC. In the following video series, Paleos, who also served as a principal investigator and study therapist for Lykos-sponsored phase 3 clinical trials of MDMA-assisted therapy in PTSD, offers his perspective on a group of 5 questions related to the upcoming August 11, 2024, PDUFA data for MDMA-assisted therapy in PTSD. The questions for each segment are as follows:
In the video segment featured above, Paleos tackles the third question. In his response, Paleos discusses the importance of addressing stigma around MDMA by conducting treatments in regulated environments with strict professional standards. He emphasizes the need for education on the intentionality of using mind-altering substances, comparing MDMA to other controlled drugs like alprazolam or opioids that have therapeutic uses. Paleos explains that the goal is to move MDMA from Schedule I to a status reflecting its medicinal value and safety when used under medical supervision. He highlights that responsible use within a medical model can reduce harm and address misconceptions about MDMA as a drug of abuse.
Relevant disclosures of interest for Paleos include Lykos Therapeutics, Fluency, Mindbloom, Nautilus Sanctuary, Nautilus Psychiatric Services, InnerMost PBC, and Journey Clinical.
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