MedPath

Psilocybin

Generic Name
Psilocybin
Brand Names
-
Drug Type
Small Molecule
Chemical Formula
C12H17N2O4P
CAS Number
520-52-5
Unique Ingredient Identifier
2RV7212BP0
Background

Psilocybin has been investigated for the treatment of Anxiety and Stage IV Melanoma. In November, 2019, it was granted Breakthrough Therapy status by the FDA.

Associated Conditions
-
Associated Therapies
-
bostonglobe.com
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What's next for MCAS and psychedelics: Opinion writers' takeaways from the ballot questions

Massachusetts' veteran-focused bill explores alternative therapies like psilocybin for mental health; Question 2's passage ends MCAS as a graduation requirement, prompting concerns over educational competence assurance; the Massachusetts Teachers Association's political influence is highlighted, urging legislative cooperation rather than resistance to voter decisions.

Psilocybin Shows Promise as OCD Treatment in Mouse Study

A study on psilocybin, a psychedelic compound, shows potential in treating OCD and Tourette’s Syndrome, with mice exhibiting reduced OCD-like behaviors and tic-like movements. The research, published in 'Molecular Psychiatry,' suggests a new treatment avenue for these conditions.
njbiz.com
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Legislators weigh change in law over 'magic mushroom' compound

New Jersey considers legalizing psilocybin for mental health treatment, with strict regulations including license requirements, medical supervision, and data collection. Research supports psilocybin's potential benefits for depression, anxiety, PTSD, and addiction. If passed, New Jersey would join Oregon and Colorado in regulating psilocybin for therapeutic use.
bunewsservice.com
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With mental health concerns on the rise, psychedelic drugs may be the answer

Massachusetts Ballot Question 4 proposes legalizing psychedelics for mental health treatment, aiming to benefit those with PTSD and other disorders. Proponents highlight potential efficiency, while opponents stress the need for more research on safety and efficacy. The debate reflects broader societal views on psychedelics as tools for healing, drawing from indigenous practices and modern clinical research.
psypost.org
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Majority of Americans support supervised use of psilocybin for mental health and well-being

A study in AJOB Neuroscience finds 89% of Americans support supervised psilocybin use for mental health treatment, and 85% for well-being enhancement, highlighting bipartisan approval. Support varies slightly with age and political leanings, with care and empathy values influencing positive views. The study cautions against hype, emphasizing the need for rigorous research and accurate claims to guide future policy.
investing.com
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Earnings call: COMPASS Pathways reports Q3 results and trial updates

COMPASS Pathways (CMPS) delays pivotal trial data for COMP360 due to recruitment challenges, now expected in Q2 2025 for COMP005 and H2 2026 for COMP006. The company focuses on COMP360's potential in treatment-resistant depression (TRD) and adjusts operations to preserve cash, including a 30% workforce reduction. COMPASS prepares for COMP360's launch, ensuring delivery centers are ready and enhancing TRD awareness. Despite challenges, the company remains confident in COMP360's development and commercial viability.
biospace.com
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Compass Delays Pivotal Trial Readouts for Psilocybin in Depression, Lays Off 30% of Staff

Compass Pathways delays Phase III readouts for its psilocybin therapy for treatment-resistant depression to 2025 and 2026, resulting in a 30% workforce reduction. The decision, influenced by increased regulatory scrutiny on functional unblinding and logistical complexities, aims to protect trial integrity. COMP360 has shown promise in earlier studies, with significant depressive symptom reduction lasting up to 12 weeks.
greenmarketreport.com
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Compass cuts 30% of staff as late-stage psilocybin drug trials face new delays

Compass Pathways to cut 30% of workforce, halt early-stage research, and focus on COMP360 Phase 3 trials; net loss widens to $38.5M; top-line data expected Q2 2025; COMP006 results delayed to H2 2026 due to increased regulatory scrutiny; restructuring follows RBC Capital Markets' 'Outperform' rating; co-founder George Goldsmith sells shares to former co-founder Lars Wilde; faces competition from Cybin Inc. and Usona Institute; R&D costs rise to $32.9M; cash reserves expected to fund operations into 2026.
medcitynews.com
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What's Next for Psychedelic Medicines?

The FDA's delay in approving MDMA-assisted therapy for PTSD highlights ongoing challenges in psychedelic medicine, but experts at HLTH 2024 suggest continued research and state initiatives may address FDA concerns, aiming for broader availability and insurance coverage.
lexology.com
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Insights for Psychedelic Stakeholders From Recent FDA Public Meeting on Advancing PTSD Treatments

On September 6, 2024, the Reagan-Udall Foundation for the FDA held a public meeting on advancing PTSD treatments, including psychedelics. Representatives from the FDA, SAMHSA, DoD, and VA discussed their initiatives, emphasizing the unmet need for effective PTSD treatments. The meeting followed the FDA's denial of Lykos Therapeutics' NDA for MDMA-AT, sparking public disappointment. The meeting highlighted federal efforts to advance PTSD research and treatment, including psychedelic research, and the urgent need for more effective mental health treatments.
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