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Please use this identifier to cite or link to this item:
https://ir.csmu.edu.tw:8080/ir/handle/310902500/22203
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Title: | Efficacy and Safety of Elvitegravir/Cobicistat/Emtricitabine/Tenofovir Disoproxil Fumarate in Asian Subjects with Human Immunodeficiency Virus 1 Infection: A Sub-Analysis of Phase 3 Clinical Trials |
Authors: | Choi, Jun Yong Sungkanuparph, Somnuek Anekthananon, Thanomsak Sax, Paul DeJesus, Edwin Edelstein, Howard Nelson, Mark DeMorin, Jennifer Liu, Hui C Swamy, Raji Bahn, Joonwoo Hwang, Sunjin Yang, Sang Youn Ng, Christopher Piontkowsky, David |
Contributors: | 中山醫學大學;醫研所 |
Keywords: | Antiretroviral therapy;Asian Elvitegravir/cobicistat/emtricitabine/tenofovir disoproxil fumarate;Human immunodeficiency virus. |
Date: | 2016-09 |
Issue Date: | 2022-03-29T03:26:59Z (UTC)
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ISSN: | 2093-2340 |
Abstract: | The efficacy and safety of a single tablet regimen (STR) of elvitegravir/cobicistat/emtricitabine/tenofovir disoproxil fumarate (E/C/F/TDF) were analyzed in Phase 3 clinical trials in antiretroviral therapy (ART)-naïve and ART-experienced Asian subjects infected with human immunodeficiency virus (HIV)-1. Studies GS-US-236-102 and GS-US-236-103 were randomized, double-blind, placebo-controlled, 144-week studies conducted in ART-naïve subjects, comparing E/C/F/TDF versus efavirenz (EFV)/F/TDF or ritonavir-boosted atazanavir (ATV+RTV) plus emtricitabine/tenofovir DF (F/TDF), respectively. Studies GS-US-236-115 and GS-US-236-121 were randomized, open-label, 96-week long conducted in ART-experienced subjects, who switched to E/C/F/TDF from ritonavir-boosted protease inhibitors (PI+RTV)+F/TDF, or non-nucleoside reverse transcriptase inhibitors (NNRTI)+F/TDF regimens. The E/C/F/TDF appeared to have sustained efficacy and safety and was well tolerated in the small number of ART-naïve and ART-experienced Asian subjects. |
URI: | https://ir.csmu.edu.tw:8080/handle/310902500/22203 |
Relation: | Infect Chemother, 48(3), 219-224 |
Appears in Collections: | [醫學研究所] 期刊論文
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