drugset / Trial / NCT00627055

Second-line Therapy Antiretroviral in Patients Who Failed Non-nucleoside Reverse Transcriptase Inhibitor (NNRTI) - Based Regimens

NCT00627055

RandomizedParallel-groupOpen-labelTreatment

Summary

To evaluate the efficacy and safety at 48 weeks between LPV/r monotherapy and 2 NRTIs + LPV/r therapy in patients failing a standard NNRTI-based treatment regimen. Also, to evaluate the short-term 24-week efficacy and safety of Lopinavir/ritonavir (LPV/r) monotherapy and 2 NRTIs+LPV/r therapy in patients failing a standard NNRTI-based treatment regimen as an interim analyses when 50% of the patients in each arm have reached 24 weeks after randomization. Last, to define risk factors for monotherapy failure in HIV-treated individuals Hypothesis. The rate of virologic suppression is not inferior in the monotherapy arm.

Timeline

Start
2008-05
Primary completion
2010-11
Completion
2010-11

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator FTC Unknown Oral
Subject LPV/r Unknown 100 mg Oral
Comparator Lamivudine Other / unclassified 150 mg Oral
Comparator Lamivudine Other / unclassified 300 mg Oral
Subject Lopinavir Other / unclassified 400 mg Oral
Comparator Tenofovir disoproxil fumarate Small molecule 300 mg Oral