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Clinical Trial Summary

The objective of this study is to demonstrate that the antibacterial activity of Sudapyridine (WX-081) is not inferior to Bedaquiline when added to a Background Regimen (BR) for treatment of rifampicin- resistant TB. Also, safety and clinical outcome will be evaluated.


Clinical Trial Description

This is a multicenter, randomized, double-blind, positive-controlled Phase III study to evaluate the efficacy and safety of Sudapyridine (WX-081) in combination with background medication (BR) in patients with rifampicin-resistant tuberculosis. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05824871
Study type Interventional
Source Shanghai Jiatan Pharmatech Co., Ltd
Contact
Status Enrolling by invitation
Phase Phase 3
Start date September 2, 2022
Completion date March 22, 2025