drugset / Trial / NCT00099632

Comparison of Three Anti-HIV Regimens to Prevent Nevirapine Resistance in Women Who Take Nevirapine During Pregnancy

NCT00099632

RandomizedParallel-groupOpen-labelTreatment

Summary

HIV infected pregnant women may take single-dose nevirapine (SD NVP) prior to giving birth to prevent mother-to-child transmission (MTCT) of HIV. However, SD NVP may cause NVP resistance in the mother, potentially ruling out some treatment options in the future. The purpose of this study is to determine which of three anti-HIV drug regimens most effectively reduces the development of maternal NVP resistance in HIV infected pregnant women. The effectiveness of short-term (7 day therapy) versus long-term (21-day therapy) regimens will also be compared. The study hypotheses are: 1) intrapartum SD NVP with a 21-day course of antiretroviral therapy (ART) results in less frequent selection of NVP-resistant HIV-1 variants than intrapartum SD NVP with a 7-day course of ART, and 2) a 7- or 21-day course of lamivudine/zidovudine (3TC/ZDV), emtricitabine/tenofovir disoproxil fumarate (FTC/TDF), or lopinavir/ritonavir (LPV/r) following SD NVP will not select nucleoside reverse transcriptase inhibitor (NRTI)- or protease inhibitor (PI)- resistant HIV-1 variants.

Timeline

Start
2006-03
Primary completion
2010-04
Completion
2011-11

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Lamivudine Other / unclassified 150 mg Oral
Subject Lopinavir Other / unclassified 133.3 mg Oral
Subject Ritonavir Other / unclassified 33.3 mg Oral
Subject Tenofovir disoproxil fumarate Small molecule 300 mg Oral
Subject Zidovudine Small molecule 300 mg Oral
Subject emtricitabine Other / unclassified 200 mg Oral
Background Nevirapine Small molecule 200 mg Oral