Researchers from Emory University, the University of Wisconsin-Madison and UC-Berkeley have identified a significant opportunity for psilocybin-assisted therapy in the U.S. mental healthcare landscape. As U.S. News reported, if approved by the FDA, psilocybin could be used to treat depression, with an estimated 5.1 to 5.6 million Americans potentially benefiting from the therapy.
Examining a group of patients undergoing treatment for depression, researchers determined that psilocybin could be a game-changing solution, particularly for individuals suffering from major depressive disorder (MDD) or treatment-resistant depression (TRD). These conditions, which affect millions across the country, are typically unresponsive to standard treatments, underscoring the urgent need for new solutions.
A Breakthrough Approach To Treating Depression
The study, published in Psychedelics by Genomic Press, explored the FDA's consideration of psilocybin from Psilocybe cubensis mushrooms as a breakthrough therapy, which is a designation that allows drugs with the potential to address life-threatening conditions like severe depression, to be fast-tracked through the approval process. If green-lighted, psilocybin would likely be reserved for individuals with the most severe forms of depression or those who have not responded to traditional treatments.
The study found that some 1.7 million Americans with TRD could immediately benefit from psilocybin-assisted therapy. When including those with MDD, the number of potential beneficiaries rises to 5.6 million. Dr. Syed Fayzan Rab, an MD candidate at Emory University and the study's lead author, highlighted the importance of recognizing the scope of this opportunity. "This underscores the importance of understanding the practical realities of rolling out this novel treatment on a large scale."
A Market Ready To Take Off
Implications of this study go beyond healthcare. The psilocybin-assisted therapy market holds immense economic potential. A 2023 report estimated that a single psilocybin-assisted therapy session could cost around $1,500 per patient. Considering the millions of individuals who may be eligible for treatment, this could translate into billions of dollars in revenue once psilocybin gains FDA approval.
Several companies are already preparing to capitalize on this potential market. Compass Pathways CMPS, Atai Life Sciences ATAI and Mindset Pharma MSSTF are among the pharmaceutical firms actively developing psilocybin-based treatments.
Beyond Depression: Psilocybin's Expanding Horizon
While psilocybin's most immediate application lies in depression treatment, its therapeutic potential extends further. Ongoing studies are investigating psilocybin's efficacy in treating chronic pain and post-traumatic stress disorder. These developments signal that psilocybin could revolutionize not just mental healthcare but also the treatment of other chronic conditions.
However, psilocybin remains classified as a Schedule I drug at the federal level, meaning it is considered to have no accepted medical use and a high potential for abuse. This classification, shared with substances like marijuana, heroin and LSD, complicates the path toward legalizing its medical use.
Despite these federal restrictions, several U.S. states and local jurisdictions have decriminalized psilocybin in recent years, signaling a growing push for policy reform at higher levels.
"It's our hope that these findings spur productive discussions and proactive preparations to optimize the benefit to patients while minimizing unintended consequences," said Dr. Charles Raison, a professor of psychiatry at the University of Wisconsin and co-author of the study.
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© 2024 Benzinga.com. Benzinga does not provide investment advice. All rights reserved.
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