Update on rilpivirine: A new potent non-nucleoside reverse transcriptase inhibitor (NNRTI) of HIV replication

被引:9
|
作者
Zaharatos, Gerasimos J. [1 ]
Wainberg, Mark A. [2 ]
机构
[1] McGill Univ, Jewish Gen Hosp, Div Infect Dis, Montreal, PQ H3T 1E2, Canada
[2] McGill Univ, AIDS Ctr, Lady Davis Inst, Jewish Gen Hosp, Montreal, PQ H3T 1E2, Canada
关键词
HIV; NNRTI; resistance; rilpivirine; treatment; TREATMENT-NAIVE; HIV-1-INFECTED PATIENTS; ECHO; PHASE-3; THRIVE; RESISTANCE; EFAVIRENZ; EFFICACY; TMC278; SAFETY;
D O I
10.3109/07853890.2012.732704
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction. A combination of antiretroviral drugs (ARVs) is necessary to achieve sustained virologic suppression of HIV viral load (< 50 copies/mL). Rilpivirine (RPV) is a potent new non-nucleoside reverse transcriptase inhibitor (NNRTI) that has the potential to be part of effective ARV combinations. Here, we review currently available data on RPV from the standpoint of virologic suppression and efficacy, drug-drug interactions safety, and resistance. Areas covered. This review presents data on the results of clinical trials involving RPV. The topics considered include antiviral potency, dosing, clinical utility, drug resistance, toxicity profile, and pharmacokinetics. Expert opinion. RPV is a potent new addition to the antiretroviral family of drugs for use in combination therapy in previously untreated HIV-infected patients. However, caution needs to be exercised in administration of RPV to patients who initiated therapy with viral loads > 100,000 viral RNA copies/mL.
引用
收藏
页码:236 / 241
页数:6
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