杜鲁特格拉维尔
替诺福韦-阿拉芬酰胺
恩曲他滨
阿巴卡韦
医学
拉米夫定
养生
药理学
人类免疫缺陷病毒(HIV)
整合酶抑制剂
病毒学
肿瘤科
内科学
病毒载量
抗逆转录病毒疗法
病毒
乙型肝炎病毒
作者
Erik De Clercq,Zhongtang Zhang,Jie Huang,Min Zhang,Guangdi Li
标识
DOI:10.1016/j.bcp.2023.115862
摘要
Bictegravir (BIC), a second-generation integrase strand-transfer inhibitor (INSTI) with high resilience to INSTI-resistance mutations, is integrated as a key component of Biktarvy® - a fixed-dose once-daily triple-drug regimen of bictegravir (BIC), emtricitabine (FTC) plus tenofovir alafenamide (TAF). Based on the accumulated evidence from HIV clinical trials and real-world studies, the clinical effectiveness of BIC + FTC + TAF has been proven non-inferior to other fixed-dose once-daily combinations such as dolutegravir + FTC + TAF and dolutegravir + abacavir + lamivudine. Biktarvy also shows limited drug-drug interactions and a high barrier to drug resistance. According to recent HIV guidelines, BIC + FTC + TAF is recommended as initial and long-term therapy for the treatment of HIV infection. For the pre-exposure prophylaxis, tenofovir disoproxil fumarate (TDF) or tenofovir alafenamide (TAF) remains advisable, but BIC may be possibly added to TDF or TAF. In the development of a long-acting once-monthly regimen, the novel nano-formulation of BIC + FTC + TAF could be possibly developed in the future.
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