The DUET trials: etravirine in the management of treatment-experienced HIV-1-infected patients

HIV therapy Pub Date : 2010-05-04 DOI:10.2217/HIV.10.14
A. Mills
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引用次数: 1

Abstract

The non-nucleoside reverse transcriptase inhibitor (NNRTI) etravirine has been approved for use in treatment-experienced, HIV-1-infected patients. The Phase III DUET trials evaluated the long-term efficacy and safety of etravirine versus placebo, each in combination with an antiretroviral background regimen including twice-daily darunavir/ritonavir 600/100 mg, in treatment-experienced patients failing therapy (with baseline plasma viral load of more than 5000 copies/ml and NNRTI and protease inhibitor resistance). At week 24 in DUET-1, 56% of etravirine-treated patients reached the primary end point of viral load below 50 copies/ml compared with 39% of placebo-treated patients (p = 0.0050); in DUET-2, response rates were 62 versus 44%, respectively (p = 0.0003). Pooled data at weeks 48 and 96 confirmed the durability of response with etravirine. With the exception of rash, the safety and tolerability profile of etravirine was similar to that of placebo over the treatment period. Etravirine is expected to ...
DUET试验:依曲维林在治疗经验的hiv -1感染患者的管理
非核苷类逆转录酶抑制剂(NNRTI) etravirine已被批准用于治疗经验丰富的hiv -1感染患者。三期DUET试验评估了依曲维林与安慰剂的长期疗效和安全性,在治疗失败的患者(基线血浆病毒载量超过5000拷贝/ml, NNRTI和蛋白酶抑制剂耐药)中,每项试验均与抗逆转录病毒背景方案联合使用,包括每日两次达鲁那韦/利托那韦600/100 mg)。在DUET-1治疗的第24周,56%的依曲维林治疗的患者达到了病毒载量低于50拷贝/ml的主要终点,而安慰剂治疗的患者为39% (p = 0.0050);在DUET-2中,有效率分别为62%和44% (p = 0.0003)。48周和96周的汇总数据证实了依曲维林反应的持久性。除皮疹外,在治疗期间,依曲维林的安全性和耐受性与安慰剂相似。Etravirine预计会…
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