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Clinical Trial Summary

This is a Phase 3, randomized, parallel-group, double-blind, placebo-controlled, 14-week study designed to evaluate the efficacy and safety of TNX-102 SL 5.6 mg (2 x 2.8 mg tablets) taken daily at bedtime for the treatment of fibromyalgia.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05273749
Study type Interventional
Source Tonix Pharmaceuticals, Inc.
Contact
Status Completed
Phase Phase 3
Start date April 6, 2022
Completion date November 14, 2023

See also
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