drugset / Trial / NCT06058299

Phase 2 Trial Assessing TBAJ876 or Bedaquiline, With Pretomanid and Linezolid in Adults With Drug-sensitive Pulmonary Tuberculosis

NCT06058299

Phase 2 Active not recruiting 309 enrolled Global Alliance for TB Drug Development
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The goal of this clinical trial is to evaluate 3 dose levels of TBAJ876 for 8 weeks in combination with pretomanid and linezolid, compared to 8 weeks of Isoniazid, rifampicin, pyrazinamide and ethambutol (2HRZE), in adult participants with newly diagnosed, smear-positive, pulmonary drug sensitive tuberculosis (DS-TB). The main questions the trial aims to answer are: * What is the optimal dose of TBAJ876 to continue further in development. * What is the bactericidal activity of bedaquiline with pretomanid and linezolid (B-Pa-L) compared to 2HRZE and TBAJ876-Pa-L over 8 weeks * What is the efficacy and safety of the 26-week B-Pa-L regimen compared with the SOC (2HRZE/4HR) in participants with DS-TB. Participants will be seen regularly during treatment (up to 26 weeks) and follow-up (52 weeks post treatment) for safety and efficacy assessments, including but not limited to: * Safety labs, ECGs, vital signs, physical exams, PK sampling, neuropathy assessments and adverse event monitoring * Sputum collection

Timeline

Start
2023-10-31
Primary completion
2024-12-27
Completion
2027-02

Drugs

EvaluationDrugModalityDoseRoute
Comparator Bedaquiline Small molecule 100 mg
Comparator Ethambutol Small molecule
Comparator Isoniazid Small molecule
Subject Linezolid Other / unclassified 600 mg
Subject Pretomanid Small molecule 200 mg
Comparator Pyrazinamide Small molecule
Comparator Rifampin Small molecule
Subject TBAJ-876 Small molecule 25 mg
Subject TBAJ-876 Small molecule 50 mg
Subject TBAJ-876 Small molecule 100 mg