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Clinical trial intelligence report
Lysergic Acid Diethylamide (LSD) in Palliative Care: a Randomised, Double-blind, Active-placebo Controlled Phase II Study (LPC-Study)
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT05883540-Jul 28, 2026
NCT ID
NCT05883540
Status
RECRUITING
Phase
Phase 2
Sponsor
University Hospital, Basel, Switzerland
Executive brief
Investment-Ready Snapshot
The LPC-Study, sponsored by the University Hospital Basel, aims to evaluate the efficacy of LSD in alleviating psychosocial distress in terminally ill patients. Given the increasing interest in psychedelic-assisted therapies, this study positions itself within a burgeoning market for mental health treatments, particularly in palliative care. The potential to demonstrate significant improvements in quality of life and pain management could attract attention from pharmaceutical companies seeking to expand their portfolios in this area. However, the competitive landscape includes other psychedelic compounds like psilocybin, which are also being investigated for similar indications. Diligence should focus on regulatory pathways, potential market access challenges, and the evolving public perception of psychedelics in therapeutic contexts.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT05883540
Indication
Palliative Care
Modality
small molecule
Target
Serotonin receptors (specifically 5-HT2A) and potential modulation of pain pathways.
Intervention
Lysergic Acid Diethylamide Tartrate, Lysergic Acid Diethylamide Tartrate
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.