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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05652907
Study type Interventional
Source FSD Pharma, Inc.
Contact
Status Terminated
Phase Phase 2
Start date January 19, 2023
Completion date May 24, 2023

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