drugset / Trial / NCT00640887

Pharmacokinetics of Rifabutin Combined With Antiretroviral Therapy in Patients With TB/HIV Co-infection in South Africa

NCT00640887

RandomizedCrossoverOpen-labelTreatment

Summary

The overall aim of the project is to evaluate rifabutin (RBT) as a replacement for rifampicin (RMP), for the combined treatment of tuberculosis and HIV infection. RBT represents an alternative to RMP for HIV infected patients as its half-life is longer and the enzymatic induction effect appears to be less important on the associated antiretroviral therapy (ART) drugs. This phase II trial is to determine precisely the pharmacokinetics parameters of RBT in combination with different ART regimens in Vietnamese HIV infected patients with pulmonary tuberculosis, in order to define optimal doses that will be further tested in a larger phase III trial comparing safety, tolerability and efficacy of RBT and RMP regimens.

Timeline

Start
2009-02
Primary completion
2010-10
Completion
2010-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Efavirenz Other / unclassified 600 mg
Subject Nevirapine Small molecule 200 mg
Subject Rifabutin Small molecule 150 mg
Subject Rifabutin Small molecule 300 mg
Subject Rifabutin Small molecule 450 mg
Subject Rifabutin Small molecule 600 mg
Subject lopinavir/ritonavir Unknown 2 unknown
Background INH Unknown
Background Lamivudine Other / unclassified
Background Stavudine Other / unclassified