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首页> 外文期刊>The Lancet >Coformulated bictegravir, emtricitabine, and tenofovir alafenamide versus dolutegravir with emtricitabine and tenofovir alafenamide, for initial treatment of HIV-1 infection (GS-US-380-1490): a randomised, double-blind, multicentre, phase 3, non-inferiority trial
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Coformulated bictegravir, emtricitabine, and tenofovir alafenamide versus dolutegravir with emtricitabine and tenofovir alafenamide, for initial treatment of HIV-1 infection (GS-US-380-1490): a randomised, double-blind, multicentre, phase 3, non-inferiority trial

机译:Coformulated Bictegravir,Emtricitabine和Tenofovir Alafenamide与eMtrickabine和替汀·韦昔洛酰胺,用于初步治疗HIV-1感染(GS-US-380-1490):随机,双盲,多期,第3期,非劣级试验

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Background Integra se strand transfer inhibitors (INSTIs) coadministered with two nucleoside or nucleotide reverse transcriptase inhibitors (NRTIs) are recommended as first-line treatment for HIV, and coformulated fixed-dose combinations are preferred to facilitate adherence. We report 48-week results from a study comparing initial HIV-1 treatment with bictegravir-a novel INSTI with a high in-vitro barrier to resistance and low potential as a perpetrator or victim of clinically relevant drug interactions-coformulated with the NRTI combination emtricitabine and tenofovir alafenamide as a fixed-dose combination to dolutegravir administered with coformulated emtricitabine and tenofovir alafenamide.
机译:背景技术建议用两种核苷或核苷酸逆转录酶抑制剂(NRTIS)共同替代核苷或核苷酸逆转录酶抑制剂(NRTIS)作为HIV的一线处理,并且Coformulated定量组合优选促进粘附。 我们报告了48周的研究结果,将初始HIV-1治疗与Bictegravir-A新insti进行了比较,其具有高体外障碍的抵抗力和低潜力作为临床相关药物与NRTI组合Emtricistabine的临床相关药物相互作用的潜在障碍或受害者 和替诺福韦醛酰胺作为用Coformulated Emtrickabine和替诺福韦醛酰胺施用的DoluteGravir的固定剂量组合。

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