drugset / Trial / NCT05652907

Safety and Efficacy of FSD201 for the Treatment of Chronic Pain Associated With Idiopathic MCAS (MCAD)

NCT05652907

Phase 2 Terminated 2 enrolled Quantum Biopharma
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study will determine if FSD201 reduces the average daily 24-hour recall pain intensity after 28 and 56 days of treatment in adults with chronic widespread musculoskeletal nociplastic pain.

Timeline

Start
2023-01-19
Primary completion
2023-05-24
Completion
2023-05-24

Drugs

EvaluationDrugModalityDoseRoute
Subject Palmidrol Small molecule 600 mg Oral