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Lack of a clinically significant drug-drug interaction in healthy volunteers between the hepatitis C virus protease inhibitor boceprevir and the HIV integrase inhibitor raltegravir

机译:在健康志愿者中,丙型肝炎病毒蛋白酶抑制剂boceprevir与HIV整合酶抑制剂raltegravir之间缺乏临床上重要的药物相互作用

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BACKGROUND: Patients coinfected with human immunodeficiency virus (HIV) and hepatitis C virus (HCV) are likely to use both HIV and HCV treatment. Drug-drug interactions have been demonstrated between boceprevir, an HCV protease inhibitor, and frequently prescribed antiretroviral drugs, such as efavirenz and boosted HIV protease inhibitors. Concomitant administration of boceprevir with these drugs should be avoided. This study was designed to investigate the absence of a drug-drug interaction between boceprevir and raltegravir, an HIV integrase inhibitor. METHODS: This was an open-label, randomized, 2-period, crossover phase 1 trial in 24 healthy volunteers. All subjects were randomly assigned to receive boceprevir 800 mg every 8 hours for 9 days plus a single dose of raltegravir 400 mg on day 10 followed by a washout period and a single dose of raltegravir 400 mg on day 38, or the same medication in reverse order. Blood samples for pharmacokinetics were collected and pharmacokinetic parameters were calculated. RESULTS: The geometric mean (GM) of raltegravir area under the concentration-time curve (AUC)(0-12h) and maximum plasma concentration (C(max)) for raltegravir + boceprevir vs raltegravir alone were 4.27 (95% confidence interval [CI], 3.22-5.66) vs 4.04 (95% CI, 3.09-5.28) mg * hour/L and 1.06 (95% CI, .76-1.49) vs 0.93 (95% CI, .70-1.23) mg/L, respectively. GM ratio estimates of raltegravir AUC(0-12h) and C(max) for raltegravir + boceprevir vs raltegravir alone were 1.04 (90% CI, .88-1.22) and 1.11 (90% CI, .91-1.36), respectively. The GM of boceprevir AUC(0-8h), C(max), and C(8h) were 5.45 (95% CI, 5.11-5.81) mg * hour/L, 1.88 (95% CI, 1.72-2.06) mg/L, and 0.09 (95% CI, .07-.11) mg/L, respectively. These data are comparable to those from historical controls. CONCLUSIONS: Due to the absence of a clinically significant drug interaction, raltegravir can be recommended for combined HIV/HCV treatment including boceprevir. CLINICAL TRIALS REGISTRATION: NCT01288417.
机译:背景:同时感染人类免疫缺陷病毒(HIV)和丙型肝炎病毒(HCV)的患者可能同时使用HIV和HCV治疗。 HCV蛋白酶抑制剂boceprevir与常用处方抗逆转录病毒药物(例如依非韦伦和加强型HIV蛋白酶抑制剂)之间已证明药物相互作用。应避免将boceprevir与这些药物并用。这项研究旨在调查boceprevir和HIV整合酶抑制剂raltegravir之间不存在药物相互作用。方法:这是一项在24位健康志愿者中进行的开放标签,随机,2期,交叉1期试验。所有受试者均被随机分配为每8小时接受Boceprevir 800 mg,共9天,再于第10天接受单剂量raltegravir 400 mg,随后是洗脱期,并在第38天接受单剂量raltegravir 400 mg,或以相同的药物反向服用订购。收集用于药代动力学的血样并计算药代动力学参数。结果:raltegravir + boceprevir与raltegravir的浓度-时间曲线(AUC)(0-12h)和最大血浆浓度(C(max))下的raltegravir区域的几何平均值(GM)为4.27(95%置信区间[ CI],3.22-5.66)vs 4.04(95%CI,3.09-5.28)mg *小时/ L和1.06(95%CI,.76-1.49)vs 0.93(95%CI,.70-1.23)mg / L , 分别。单独使用raltegravir + boceprevir与raltegravir相比,raltegravir AUC(0-12h)和C(max)的GM比估计分别为1.04(90%CI,.88-1.22)和1.11(90%CI,.91-1.36)。 boceprevir AUC(0-8h),C(max)和C(8h)的GM为5.45(95%CI,5.11-5.81)mg *小时/ L,1.88(95%CI,1.72-2.06)mg / L和0.09(95%CI,.07-.11)mg / L。这些数据可与历史对照的数据进行比较。结论:由于缺乏临床上重要的药物相互作用,可推荐使用拉格列韦用于包括boceprevir在内的HIV / HCV联合治疗。临床试验注册:NCT01288417。

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