drugset / Trial / NCT00643968

Tenofovir DF + Efavirenz (TDF+EFV) Versus Tenofovir DF + Efavirenz + Lamivudine (TDF+EFV+3TC) Maintenance Regimen in Virologically Controlled Patients: COOL Trial

NCT00643968

Phase 4 Completed 140 enrolled Gilead Sciences
RandomizedParallel-groupOpen-label

Summary

Primary objective: Evaluation of the efficacy of TDF+3TC+EFV versus TDF+EFV QD to maintain plasma HIV-1 RNA BLQ (\< 50 copies/mL) (c/mL) at 48 weeks (W48) Main Secondary objectives: Comparison of the two arms for genotypic resistance profile in case of virological failure CD4 changes from baseline Evolution of the lipid profile and morphological changes in fat distribution, and safety Efficacy and genotypic profile data, results of lipid markers, morphological changes and main biological parameters

Timeline

Start
2003-03
Primary completion
2005-06
Completion
2005-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Lamivudine Other / unclassified
Comparator Efavirenz Other / unclassified
Comparator Tenofovir disoproxil fumarate Small molecule