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Clinical Trial Summary

The primary objective of this study is to evaluate the efficacy of switching to a fixed-dose combination (FDC) of bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF) versus continuing on a regimen consisting of boosted atazanavir (ATV) or darunavir (DRV) plus either emtricitabine/tenofovir disoproxil fumarate (FTC/TDF) or abacavir/lamivudine (ABC/3TC) in HIV-1 infected adults who are virologically suppressed.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02603107
Study type Interventional
Source Gilead Sciences
Contact
Status Completed
Phase Phase 3
Start date November 20, 2015
Completion date December 23, 2019

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