drugset / Trial / NCT07069582

Pharmacokinetics of Antituberculosis Drugs in Breastfeeding Women

NCT07069582

RandomizedParallel-groupOpen-labelTreatment

Summary

This study is a sub-study of the SSTARLET trial (NCT06498414). The overall aim is to assess the pharmacokinetic profiles after taking a single dose of rifampicin, isoniazid, levofloxacin, rifapentine, and bedaquiline in breastfeeding women and the excretion of these drugs in breast milk, with the hope of including breastfeeding women in future clinical trials of TPT, including expanding the inclusion criteria of the SSTARLET trial. In this study, healthy breastfeeding women who fulfill the eligibility criteria will be enrolled from several primary health care centers in Bandung, which will be referred to the TB Research Clinic of the Universitas Padjadjaran, Bandung, Indonesia. Ten participants will be randomized to each of the following six study arms: * Arm A: Single-dose rifampicin at 10 mg/kg body weight (RIF10). * Arm B: Single-dose rifampicin at 20 mg/kg body weight (RIF20). * Arm C: Single-dose isoniazid at 5 mg/kg body weight (INH5). * Arm D: Single-dose levofloxacin at 10-15 mg/kg body weight (LFX10-15). * Arm E: Single-dose rifapentine at 10 mg/kg body weight (RPT10). * Arm F: Single-dose bedaquiline at 400 mg (BDQ400).

Timeline

Start
2026-04-01
Primary completion
2026-10-31
Completion
2026-10-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Bedaquiline Small molecule 400 mg Oral
Subject Isoniazid Small molecule 5 mg/kg Oral
Subject Levofloxacin Small molecule Oral
Subject Rifampin Small molecule 10 mg/kg Oral
Subject Rifampin Small molecule 20 mg/kg Oral
Subject Rifapentine Small molecule 10 mg/kg Oral

Indications