drugset / Trial / NCT02431247

A Study to Evaluate Efficacy and Safety of Darunavir/Cobicistat/Emtricitabine/Tenofovir Alafenamide (D/C/F/TAF) Fixed Dose Combination (FDC) Versus a Regimen Consisting of Darunavir/Cobicistat FDC With Emtricitabine/Tenofovir Disoproxil Fumarate FDC in Treatment-naive HIV Type 1 Infected Subjects

NCT02431247 ↗

Phase 3 Completed 725 enrolled Janssen Sciences Ireland UC
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to demonstrate non-inferiority in efficacy of a darunavir/cobicistat/emtricitabine/tenofovir alafenamide (D/C/F/TAF) fixed dose combination (FDC) tablet versus Darunavir/Cobicistat (DRV/COBI) FDC coadministered with Emtricitabine/tenofovir disoproxil fumarate (FTC/TDF) FDC in human immunodeficiency virus-1 (HIV-1) infected, antiretroviral (ARV) treatment naive adult participants.

Timeline

Start
2015-07-06
Primary completion
2017-03-02
Completion
2020-09-30

Outcome

Met primary endpoint

registry p < 0.001; Difference in percentage 2.7 (95% CI -1.6 to 7.1) NCT02431247 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Cobicistat Small molecule 150 mg Oral
Subject Darunavir Small molecule 800 mg Oral
Comparator FTC/TDF FDC Unknown 300 mg Oral
Subject emtricitabine Other / unclassified 200 mg Oral
Subject tenofovir alafenamide Small molecule 10 mg Oral