drugset / Trial / NCT02651259
Evaluating PK, Tolerability, and Safety of Rifapentine and Isoniazid in Pregnant and Postpartum Women
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Isoniazid | Small molecule | 900 mg | — |
| Subject | Rifapentine | Small molecule | 900 mg | — |