drugset / Trial / NCT02354014

Pharmacokinetic Study to Evaluate Anti-mycobacterial Activity of TMC207 in Combination With Background Regimen (BR) of Multidrug Resistant Tuberculosis (MDR-TB) Medications for Treatment of Children/Adolescents With Pulmonary MDR-TB

NCT02354014

Phase 2 Recruiting 60 enrolled Janssen Research & Development, LLC
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (explores what the body does to the drug), and anti-mycobacterial activity of bedaquiline (TMC207) in children and adolescents (0 months to less than \[\<\] 18 years of age) diagnosed with confirmed or probable pulmonary multidrug resistant tuberculosis (MDR-TB), in combination With a Background Regimen (BR) of MDR-TB Medications.

Timeline

Start
2016-05-03
Primary completion
2027-02-11
Completion
2028-11-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Bedaquiline Small molecule 4 mg/kg Oral
Subject Bedaquiline Small molecule 100 mg Oral
Subject Bedaquiline Small molecule 200 mg Oral