drugset / Trial / NCT01497899
Safety and Efficacy of E/C/F/TAF (Genvoya®) Versus E/C/F/TDF (Stribild®) in HIV-1 Infected, Antiretroviral Treatment-Naive Adults
RandomizedParallel-groupDouble-blindTreatment
Summary
The primary objective of this study is to evaluate the efficacy of elvitegravir/cobicistat/emtricitabine/tenofovir alafenamide (Genvoya®; E/C/F/TAF) fixed-dose combination (FDC) versus elvitegravir/cobicistat/emtricitabine/tenofovir disoproxil fumarate (Stribild®; E/C/F/TDF) FDC in HIV-1 infected, antiretroviral treatment-naive adults.
Timeline
- Start
- 2011-12-28
- Primary completion
- 2012-10-17
- Completion
- 2016-08-22
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | E/C/F/TAF | Unknown | 10 mg | Oral |
| Subject | E/C/F/TAF | Unknown | 150 mg | Oral |
| Subject | E/C/F/TAF | Unknown | 200 mg | Oral |
| Comparator | E/C/F/TDF | Unknown | 150 mg | Oral |
| Comparator | E/C/F/TDF | Unknown | 200 mg | Oral |
| Comparator | E/C/F/TDF | Unknown | 300 mg | Oral |