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Treatment Outcomes and Plasma Level of Ritonavir-boosted Lopinavir Monotherapy Among HIV-infected Patients Who Had Non-nucleoside Reverse Transcriptase Inhibitor (NRTI) and NNRTI Failure: A Pilot Study
To assess 48-week treatment responses, tolerability, and steady-state minimum plasma concentrations of ritonavir-boosted lopinavir monotherapy for salvage therapy in HIV-1 infected patients who failed antiretroviral regimens containing NRTI and NNRTI.
Details
| Lead sponsor | Bamrasnaradura Infectious Diseases Institute |
|---|---|
| Phase | Phase 3 |
| Status | COMPLETED |
| Enrolment | 40 |
| Start date | 2007-04 |
| Completion | 2011-02 |
Conditions
- HIV
Interventions
- lopinavir/ritonavir soft gel capsule
Primary outcomes
- To assess 48-week treatment responses of ritonavir-boosted lopinavir (LPV/r) monotherapy as salvage regimen. — 48 weeks
Countries
Thailand