Switching from tenofovir disoproxil fumarate to tenofovir alafenamide coformulated with rilpivirine and emtricitabine in virally suppressed adults with HIV-1 infection: a randomised, double-blind, multicentre, phase 3b, non-inferiority study

Summary Background Tenofovir alafenamide, a tenofovir prodrug, results in 90% lower tenofovir plasma concentrations than does tenofovir disproxil fumarate, thereby minimising bone and renal risks. We investigated the efficacy, safety, and tolerability of switching to a single-tablet regimen containi...

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Veröffentlicht in:The lancet HIV 2017-05, Vol.4 (5), p.e195-e204
Hauptverfasser: Orkin, Chloe, MD, DeJesus, Edwin, MD, Ramgopal, Moti, MD, Crofoot, Gordon, MD, Ruane, Peter, MD, LaMarca, Anthony, MD, Mills, Anthony, MD, Vandercam, Bernard, MD, de Wet, Joseph, MD, Rockstroh, Jürgen, MD, Lazzarin, Adriano, MD, Rijnders, Bart, MD, Podzamczer, Daniel, MD, Thalme, Anders, MD, Stoeckle, Marcel, MD, Porter, Danielle, PhD, Liu, Hui C, PhD, Cheng, Andrew, MD, Quirk, Erin, MD, SenGupta, Devi, MD, Cao, Huyen, Dr
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Sprache:eng
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Zusammenfassung:Summary Background Tenofovir alafenamide, a tenofovir prodrug, results in 90% lower tenofovir plasma concentrations than does tenofovir disproxil fumarate, thereby minimising bone and renal risks. We investigated the efficacy, safety, and tolerability of switching to a single-tablet regimen containing rilpivirine, emtricitabine, and tenofovir alafenamide compared with remaining on rilpivirine, emtricitabine, and tenofovir disoproxil fumarate. Methods In this randomised, double-blind, multicentre, placebo-controlled, non-inferiority trial, HIV-1-infected adults were screened and enrolled at 119 hospitals in 11 countries in North America and Europe. Participants were virally suppressed (HIV-1 RNA
ISSN:2352-3018
2352-3018
DOI:10.1016/S2352-3018(17)30031-0