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A 48 Week, Randomized, Open-label, 2 Arm Study to Compare the Efficacy, Safety and Tolerability of HAART Containing Nevirapine 400mg/Day Versus Nevirapine 600 mg/Day in HIV-1 Infected Patients Started at 2-6 Weeks After Initiating Rifampin Containing Antituberculous Therapy
A 48 week, randomized, open-label, two arm study to compare the efficacy, safety and tolerability of HAART containing nevirapine 400 mg/day versus nevirapine 600 mg/day in HIV-1 infected patients started at 2-6 weeks after initiating rifampicin containing antituberculosis therapy.
Details
| Lead sponsor | The HIV Netherlands Australia Thailand Research Collaboration |
|---|---|
| Phase | Phase 2 |
| Status | COMPLETED |
| Enrolment | 42 |
| Start date | 2005-10 |
| Completion | 2009-12 |
Conditions
- HIV Infections
- Tuberculosis
Interventions
- HAART containing nevirapine
Primary outcomes
- Efficacy of nevirapine based HAART 400 mg/day versus 600 mg/day on HIV-1 load as measured by HIV-1 RNA quantification in plasma — 48 weeks
Countries
Thailand