Efficacy and Safety of Switching to Dolutegravir/Lamivudine Versus Continuing a Tenofovir Alafenamide-Based Regimen in Virologically Suppressed Adults With Human Immunodeficiency Virus Type 1: Subgroup Analysis of Participants With Elvitegravir as Baseline Third Agent From the TANGO Study

被引:0
作者
Ait-Khaled, Mounir [1 ]
Oyee, James [2 ]
Ooi, Adrian Yit Reen [3 ]
Wynne, Brian [4 ]
Maldonado, Andres [5 ]
Jones, Bryn [1 ]
Wang, Tao [6 ]
机构
[1] ViiV Healthcare, 980 Great West Rd, Brentford TW8 9GS, Middx, England
[2] GSK, Brentford, England
[3] ViiV Healthcare, Singapore, Singapore
[4] ViiV Healthcare, Durham, NC USA
[5] ViiV Healthcare, Wavre, Belgium
[6] GSK, Shanghai, Peoples R China
关键词
dolutegravir/lamivudine; elvitegravir; HIV-1; switch study; virologically suppressed; ANTIRETROVIRAL THERAPY; DISOPROXIL FUMARATE; HIV; DYSLIPIDEMIA; COBICISTAT; LAMIVUDINE; INFECTION; RISK;
D O I
10.1093/ofid/ofae227
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
TANGO results have established the durable efficacy of dolutegravir/lamivudine in virologically suppressed individuals who switched from 3- or 4-drug tenofovir alafenamide (TAF)-based regimens. In this post hoc subgroup analysis, 144-week efficacy and tolerability of dolutegravir/lamivudine in participants who switched from elvitegravir/cobicistat/emtricitabine/TAF were consistent with the overall switch population.Clinical Trials Registration NCT03446573.
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