drugset / Trial / NCT00365612

Single Tablet Regimen (STR) Simplification Study for HIV-1 Infected Patients

NCT00365612 ↗

Phase 4 Completed 300 enrolled Gilead Sciences Bristol-Myers Squibb · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

To compare the effectiveness (efficacy, safety \& tolerability) of a Single Tablet Regimen of efavirenz/emtricitabine/tenofovir DF to subjects continuing on unmodified HAART as measured by the proportion of patients who maintain viral load (HIV-1 RNA) \<200 copies/mL at Week 48.

Timeline

Start
2006-07
Primary completion
2007-10
Completion
2008-01

Outcome

Met primary endpoint

paper difference (95% confidence interval) between arms of 1.1% (-6.7% to 8.8%), indicating noninferiority of EFV/FTC/TDF vs. SBR. PMID 19357529 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Efavirenz Other / unclassified — —
Subject Tenofovir disoproxil fumarate Small molecule — —
Subject emtricitabine Other / unclassified — —