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No Clinically Relevant Drug-Drug Interactions between Methadone or Buprenorphine-Naloxone and Antiviral Combination Glecaprevir and Pibrentasvir.美沙酮或丁丙诺啡-纳洛酮与抗病毒复方加拉夫定和哌仑他韦之间无临床相关的药物相互作用。
Antimicrob Agents Chemother. 2017 Sep 22;61(10). doi: 10.1128/AAC.00958-17. Print 2017 Oct.
2
Efficacy of Glecaprevir/Pibrentasvir for 8 or 12 Weeks in Patients With Hepatitis C Virus Genotype 2, 4, 5, or 6 Infection Without Cirrhosis.Glecaprevir/Pibrentasvir 治疗 8 或 12 周对无肝硬化的 2、4、5 或 6 型丙型肝炎病毒感染患者的疗效。
Clin Gastroenterol Hepatol. 2018 Mar;16(3):417-426. doi: 10.1016/j.cgh.2017.09.027. Epub 2017 Sep 22.
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Resistance Analysis of a 3-Day Monotherapy Study with Glecaprevir or Pibrentasvir in Patients with Chronic Hepatitis C Virus Genotype 1 Infection.慢性丙型肝炎病毒基因 1 型感染患者使用格卡瑞韦或哌仑他韦进行 3 天单药治疗的耐药性分析。
Viruses. 2018 Aug 28;10(9):462. doi: 10.3390/v10090462.
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Glecaprevir-pibrentasvir to treat chronic hepatitis C virus infection in Asia: two multicentre, phase 3 studies- a randomised, double-blind study (VOYAGE-1) and an open-label, single-arm study (VOYAGE-2).格卡瑞韦哌仑他韦治疗亚洲慢性丙型肝炎病毒感染:两项多中心、3 期研究-一项随机、双盲研究(VOYAGE-1)和一项开放标签、单臂研究(VOYAGE-2)。
Lancet Gastroenterol Hepatol. 2020 Sep;5(9):839-849. doi: 10.1016/S2468-1253(20)30086-8. Epub 2020 Jul 16.
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Glecaprevir and pibrentasvir yield high response rates in patients with HCV genotype 1-6 without cirrhosis.格卡瑞韦和哌仑他韦在无肝硬化的 HCV 基因 1-6 型患者中产生高应答率。
J Hepatol. 2017 Aug;67(2):263-271. doi: 10.1016/j.jhep.2017.03.039. Epub 2017 Apr 13.
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Effect of steady-state faldaprevir on the pharmacokinetics of steady-state methadone and buprenorphine-naloxone in subjects receiving stable addiction management therapy.稳态法达普韦对接受稳定成瘾管理治疗的受试者中稳态美沙酮和丁丙诺啡-纳洛酮药代动力学的影响。
Antimicrob Agents Chemother. 2015 Jan;59(1):498-504. doi: 10.1128/AAC.04046-14. Epub 2014 Nov 10.
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Drug-Drug Interactions of Glecaprevir and Pibrentasvir Coadministered With Human Immunodeficiency Virus Antiretrovirals.格拉瑞韦和比仑他韦与抗人类免疫缺陷病毒(HIV)逆转录酶抑制剂联合用药的药物-药物相互作用。
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Glecaprevir + pibrentasvir (ABT493 + ABT-530) for the treatment of Hepatitis C.格卡瑞韦哌仑他韦(ABT-493 + ABT-530)治疗丙型肝炎。
Expert Rev Gastroenterol Hepatol. 2018 Jan;12(1):9-17. doi: 10.1080/17474124.2018.1411802. Epub 2017 Dec 5.
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Glecaprevir-Pibrentasvir for 8 or 12 Weeks in HCV Genotype 1 or 3 Infection.格卡瑞韦哌仑他韦片治疗 8 或 12 周用于治疗 1 型或 3 型丙型肝炎病毒感染。
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J Clin Transl Hepatol. 2020 Sep 28;8(3):322-335. doi: 10.14218/JCTH.2020.00034. Epub 2020 Jul 30.
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Clin Infect Dis. 2018 Sep 14;67(7):1010-1017. doi: 10.1093/cid/ciy220.

本文引用的文献

1
Glecaprevir and pibrentasvir yield high response rates in patients with HCV genotype 1-6 without cirrhosis.格卡瑞韦和哌仑他韦在无肝硬化的 HCV 基因 1-6 型患者中产生高应答率。
J Hepatol. 2017 Aug;67(2):263-271. doi: 10.1016/j.jhep.2017.03.039. Epub 2017 Apr 13.
2
Glecaprevir and pibrentasvir for 12 weeks for hepatitis C virus genotype 1 infection and prior direct-acting antiviral treatment.glecaprevir和pibrentasvir治疗丙型肝炎病毒1型感染及既往直接抗病毒治疗12周。
Hepatology. 2017 Aug;66(2):389-397. doi: 10.1002/hep.29081. Epub 2017 Apr 10.
3
Assessment of drug-drug interactions between daclatasvir and methadone or buprenorphine-naloxone.达卡他韦与美沙酮或丁丙诺啡-纳洛酮之间药物相互作用的评估。
Antimicrob Agents Chemother. 2015 Sep;59(9):5503-10. doi: 10.1128/AAC.00478-15. Epub 2015 Jun 29.
4
Chronic hepatitis C virus infection in the United States, National Health and Nutrition Examination Survey 2003 to 2010.美国慢性丙型肝炎病毒感染,2003 年至 2010 年全国健康和营养调查。
Ann Intern Med. 2014 Mar 4;160(5):293-300. doi: 10.7326/M13-1133.
5
Buprenorphine metabolites, buprenorphine-3-glucuronide and norbuprenorphine-3-glucuronide, are biologically active.丁丙诺啡代谢物,丁丙诺啡-3-葡萄糖醛酸苷和去甲丁丙诺啡-3-葡萄糖醛酸苷,具有生物活性。
Anesthesiology. 2011 Dec;115(6):1251-60. doi: 10.1097/ALN.0b013e318238fea0.
6
(R)-methadone versus racemic methadone: what is best for patient care?(R)-美沙酮与外消旋美沙酮:哪一种更适合患者治疗?
Addiction. 2011 Apr;106(4):687-8. doi: 10.1111/j.1360-0443.2011.03374.x.
7
Glucuronidation of buprenorphine and norbuprenorphine by human liver microsomes and UDP-glucuronosyltransferases.人肝微粒体和尿苷二磷酸葡萄糖醛酸基转移酶对丁丙诺啡和去甲丁丙诺啡的葡萄糖醛酸化作用。
Drug Metab Lett. 2009 Apr;3(2):101-7. doi: 10.2174/187231209788654117.
8
Clinical pharmacology of methadone for pain.美沙酮用于镇痛的临床药理学
Acta Anaesthesiol Scand. 2008 Aug;52(7):879-89. doi: 10.1111/j.1399-6576.2008.01597.x. Epub 2008 Mar 7.
9
Determination of drug glucuronidation and UDP-glucuronosyltransferase selectivity using a 96-well radiometric assay.使用96孔放射性测定法测定药物葡萄糖醛酸化和UDP-葡萄糖醛酸基转移酶选择性。
Drug Metab Dispos. 2005 Jun;33(6):812-9. doi: 10.1124/dmd.105.004333. Epub 2005 Mar 23.
10
Population pharmacokinetics of (R)-, (S)- and rac-methadone in methadone maintenance patients.美沙酮维持治疗患者中(R)-、(S)-和消旋美沙酮的群体药代动力学
Br J Clin Pharmacol. 2004 Jun;57(6):742-55. doi: 10.1111/j.1365-2125.2004.02079.x.

美沙酮或丁丙诺啡-纳洛酮与抗病毒复方加拉夫定和哌仑他韦之间无临床相关的药物相互作用。

No Clinically Relevant Drug-Drug Interactions between Methadone or Buprenorphine-Naloxone and Antiviral Combination Glecaprevir and Pibrentasvir.

机构信息

AbbVie Inc., North Chicago, Illinois, USA.

INC Research, Toronto, Ontario, Canada.

出版信息

Antimicrob Agents Chemother. 2017 Sep 22;61(10). doi: 10.1128/AAC.00958-17. Print 2017 Oct.

DOI:10.1128/AAC.00958-17
PMID:28807904
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5610490/
Abstract

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.

摘要

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。