In this part of our 5-part series, Gus Alva, MD discusses the next steps in research for long-term effects and broader applications of MDMA-assisted therapy.
As August 11, 2024 approaches, the psychiatric community, and public health as a whole, wait with anticipation surrounding the US Food and Drug Administration’s decision on 3,4-methylenedioxymethamphetamine (MDMA)-assisted therapy in the management of posttraumatic stress disorder (PTSD).
A subject mired in controversy as a result of decades-old stigma, MDMA-assisted therapy has, with extensive research efforts and clinical trial data, proven its potential. Beyond MDMA-assisted therapies, clinical programs and trials for other psychedelic agents, including psilocybin, ketamine, and other compounds, have furthered discussions around the roles of these therapeutic options in psychiatric care.
Backed by positive data from the phase 3, randomized, double-blind, placebo-controlled MAPP1 and MAPP2 trials, the application for MDMA-assisted therapy PTSD seemed poise to usher in a new era in management.
However, the road to a potential approval has seemingly turned into an even greater uphill battle in the wake of an FDA Psychopharmacologic Advisory Committee on June 4, 2024, which saw the committee vote 2-9 against supporting the effectiveness of MDMA in the treatment of adult patients with PTSD followed by a subsequent 1 to 10 vote against the notion that the benefits of MDMA in combination with the FDA’s proposed risk evaluation and mitigation strategy (REMS) outweigh its risks for the treatment of patients with PTSD.
Despite this, leading researchers, psychiatrists, as well as patients and advocacy organizations, have vocalized their concerns surrounding the unmet need in PTSD management and the need to research further the use of psychedelic therapies for use in psychiatric conditions.
In this 5-part video series, we spotlight the perspective of leading subject matter expert Gus Alva, MD, a psychiatrist and medical director of ATP Clinical Research, on the subject, with segments dedicated to:
In this final segment, Alva discusses the critical need for long-term data on MDMA-assisted therapy, emphasizing the importance of understanding potential long-term effects. The conversation highlights concerns about the possibility of negative outcomes over extended periods, which underscores the necessity for ongoing research. Despite these concerns, Alva acknowledges the promising data already available, which extends beyond PTSD to other conditions like alcohol dependence.
The discussion touches on the potential benefits of MDMA-assisted therapy for various psychiatric and addiction disorders, advocating for a cautious yet open-minded approach. Alva also mentions the importance of adhering to established psychotherapeutic guidelines to ensure safe and effective treatment. The segment concludes by stressing the need for post-marketing studies to monitor long-term outcomes and fulfill regulatory commitments, ultimately aiming to broaden the therapeutic applications of MDMA in a controlled and scientifically sound manner.
Relevant disclosures for Alva include Teva Pharmaceuticals, Otsuka America Pharmaceuticals, AbbVie Inc., Axsome Therapeutics, Janssen Pharmaceuticals, and more.
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