AbbVie Inc., North Chicago, Illinois, USA.
INC Research, Toronto, Ontario, Canada.
Antimicrob Agents Chemother. 2017 Sep 22;61(10). doi: 10.1128/AAC.00958-17. Print 2017 Oct.
The combination of glecaprevir (formerly ABT-493), a nonstructural protein 3/4A (NS3/4A) protease inhibitor, and pibrentasvir (formerly ABT-530), an NS5A protein inhibitor, is being developed as treatment for HCV genotype 1 to 6 infection. The pharmacokinetics, pharmacodynamics, safety, and tolerability of methadone or buprenorphine-naloxone when coadministered with the glecaprevir-pibrentasvir combination in HCV-negative subjects on stable opioid maintenance therapy were investigated in a phase 1, single-center, two-arm, multiple-dose, open-label sequential study. Subjects received methadone (arm 1) or buprenorphine-naloxone (arm 2) once daily (QD) per their existing individual prescriptions alone (days 1 to 9) and then in combination with glecaprevir at 300 mg QD and pibrentasvir at 120 mg QD (days 10 to 16) each morning. Dose-normalized exposures were similar with and without glecaprevir and pibrentasvir for ()- and ()-methadone (≤5% difference) and for buprenorphine and naloxone (≤24% difference); the norbuprenorphine area under the curve was 30% higher with glecaprevir and pibrentasvir, consistent with maximum and trough plasma concentrations that increased by 21% to 25%. No changes in pupil response, short opiate withdrawal scale score, or desire for drugs questionnaire were observed when glecaprevir and pibrentasvir were added to methadone or buprenorphine-naloxone therapy. No dose adjustment is required when glecaprevir and pibrentasvir are coadministered with methadone or buprenorphine-naloxone.
格卡瑞韦(前体药物 ABT-493)和帕利瑞韦(前体药物 ABT-530)联合制剂用于治疗 HCV 基因型 1-6 感染,其中格卡瑞韦为非结构蛋白 3/4A(NS3/4A)蛋白酶抑制剂,帕利瑞韦为 NS5A 蛋白抑制剂。本研究采用一项开放标签、两臂、多剂量、单中心、Ⅰ期临床试验,评估在稳定接受阿片类药物维持治疗的 HCV 阴性人群中,合并使用格卡瑞韦和帕利瑞韦对美沙酮或丁丙诺啡-纳洛酮药代动力学、药效动力学、安全性和耐受性的影响。受试者每天分别接受一次美沙酮(第 1 天至第 9 天)或丁丙诺啡-纳洛酮(第 1 天至第 9 天)治疗,按照各自的个体化处方剂量用药,然后合用格卡瑞韦 300mg QD 和帕利瑞韦 120mg QD(第 10 天至第 16 天)。与未合用格卡瑞韦和帕利瑞韦相比,合用格卡瑞韦和帕利瑞韦时()-和()-美沙酮(差异≤5%)和丁丙诺啡、纳洛酮(差异≤24%)的剂量校正后暴露量相似;与未合用格卡瑞韦和帕利瑞韦相比,合用格卡瑞韦和帕利瑞韦时,去甲羟丁丙诺啡的 AUC 增加 30%,最大和最小血浆浓度分别增加 21%至 25%。合用格卡瑞韦和帕利瑞韦后,美沙酮或丁丙诺啡-纳洛酮治疗时瞳孔反应、短期阿片类戒断量表评分或药物渴求问卷无变化。合用格卡瑞韦和帕利瑞韦时无需调整美沙酮或丁丙诺啡-纳洛酮剂量。