drugset / Trial / NCT00358917

Study of Lopinavir/Ritonavir Tablets Comparing Once-Daily Versus Twice-Daily Administration When Coadministered With Nucleoside/Nucleotide Reverse Transcriptase Inhibitors in Antiretroviral-Experienced Human Immunodeficiency Virus Type 1 Infected Subjects

NCT00358917

Phase 3 Completed 599 enrolled Abbott
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study was to compare the safety, tolerability, and antiviral activity of once-daily (QD) and twice-daily (BID) dosing of the lopinavir/ritonavir (LPV/r) tablet formulation in combination with nucleoside/nucleotide reverse transcriptase inhibitors (NRTIs) in antiretroviral-experienced human immunodeficiency virus type 1 infected subjects with detectable viral load while receiving their current antiretroviral therapy.

Timeline

Start
2006-08
Primary completion
2008-11
Completion
2008-11

Drugs

EvaluationDrugModalityDoseRoute
Comparator Lopinavir Other / unclassified 400 mg
Comparator Lopinavir Other / unclassified 800 mg
Comparator Ritonavir Other / unclassified 100 mg
Comparator Ritonavir Other / unclassified 200 mg