drugset / Trial / NCT02651259

Evaluating PK, Tolerability, and Safety of Rifapentine and Isoniazid in Pregnant and Postpartum Women

NCT02651259

Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study was to evaluate the pharmacokinetics (PK), tolerability, and safety of once-weekly doses of rifapentine (RPT) and isoniazid (INH) in HIV-1-infected and HIV-1-uninfected pregnant and postpartum women with latent tuberculosis (TB).

Timeline

Start
2017-03-13
Primary completion
2019-04-10
Completion
2019-04-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Isoniazid Small molecule 900 mg
Subject Rifapentine Small molecule 900 mg

Indications