If you are a drug manufacturer dealing with the lack of effective treatments for end-of-life anxiety — this project developed a standardized therapy manual and GMP-certified drug delivery process that ensures patient safety and consistent results.
Psilocybin Therapy System for Psychological Distress in End-of-Life Care
Imagine a mental reset button for people facing the end of their lives with severe anxiety or depression. This project uses a controlled dose of a psychedelic compound to help patients find peace when standard medicines fail. It's like providing a guided emotional journey to ease the heaviest burdens of terminal illness.
What needed solving
Palliative care patients with COPD, ALS, and MS suffer from severe psychological distress that current drugs cannot treat. This creates a gap in care that reduces quality of life for patients and families.
What was built
A standardized therapy manual, a digital care platform, and a GMP-certified drug delivery system for psilocybin.
Who needs this
Who can put this to work
If you are a tech provider dealing with fragmented post-treatment care — this project developed a digital care platform and peer-support networks that maintain patient wellbeing after the clinical session.
If you are a clinic owner dealing with high patient distress in COPD or ALS cases — this project developed a trained therapist model and clinical protocol that can be integrated into care services to improve quality of life.
Quick answers
What is the cost or price of this therapy?
Based on available project data, specific pricing is not mentioned, but the project aims to create a cost-effective deployment model for European healthcare systems.
Can this be scaled to an industrial level?
The project uses a multi-centre trial across 4 countries and GMP-certified drug manufacturing, suggesting a scalable clinical model.
What are the IP and licensing options?
Based on available project data, specific patents are not listed, but the project has produced a standardized therapy manual and a digital care platform.
What regulatory hurdles have been cleared?
The project has secured full regulatory and ethical approval in the Netherlands, Denmark, Portugal, and the Czech Republic.
What is the timeline for implementation?
The project runs from 2024-01-01 to 2027-12-31, with the first 18 months focused on establishing the operational foundation.
Who built it
The consortium is heavily weighted toward clinical and academic expertise, featuring 20 partners across 8 countries. With 6 universities and 3 research centers, the focus is scientific validation, though the inclusion of 3 SMEs and a 15% industry ratio indicates a clear path toward commercial translation and practical application in healthcare settings.
Contact Academisch Ziekenhuis Groningen in the Netherlands
Talk to the team behind this work.
Contact us to explore licensing the therapy manual or digital platform.