Literature DB >> 28807904

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

Matthew P Kosloski1, Weihan Zhao1, Armen Asatryan1, Jens Kort1, Pierre Geoffroy2, Wei Liu3.   

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 (R)- and (S)-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.
Copyright © 2017 American Society for Microbiology.

Entities:  

Keywords:  HCV; buprenorphine; glecaprevir; methadone; naloxone; pharmacokinetics; pibrentasvir

Mesh:

Substances:

Year:  2017        PMID: 28807904      PMCID: PMC5610490          DOI: 10.1128/AAC.00958-17

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  17 in total

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2.  Prevalence and duration of hepatitis C among injection drug users in San Francisco, Calif.

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3.  The development of a Short Opiate Withdrawal Scale (SOWS).

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4.  Buprenorphine metabolites, buprenorphine-3-glucuronide and norbuprenorphine-3-glucuronide, are biologically active.

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5.  Assessment of drug-drug interactions between daclatasvir and methadone or buprenorphine-naloxone.

Authors:  T Garimella; R Wang; W-L Luo; P Wastall; H Kandoussi; M DeMicco; R D Bruce; C Hwang; R Bertz; M Bifano
Journal:  Antimicrob Agents Chemother       Date:  2015-06-29       Impact factor: 5.191

6.  Glucuronidation of buprenorphine and norbuprenorphine by human liver microsomes and UDP-glucuronosyltransferases.

Authors:  Yan Chang; David E Moody
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Review 8.  Clinical pharmacology of methadone for pain.

Authors:  O M S Fredheim; K Moksnes; P C Borchgrevink; S Kaasa; O Dale
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Review 9.  Action of opiates on gastrointestinal function.

Authors:  L Bueno; J Fioramonti
Journal:  Baillieres Clin Gastroenterol       Date:  1988-01

10.  Chronic hepatitis C virus infection in the United States, National Health and Nutrition Examination Survey 2003 to 2010.

Authors:  Maxine M Denniston; Ruth B Jiles; Jan Drobeniuc; R Monina Klevens; John W Ward; Geraldine M McQuillan; Scott D Holmberg
Journal:  Ann Intern Med       Date:  2014-03-04       Impact factor: 25.391

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  2 in total

1.  Efficacy and Safety of Glecaprevir/Pibrentasvir in Patients Coinfected With Hepatitis C Virus and Human Immunodeficiency Virus Type 1: The EXPEDITION-2 Study.

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Journal:  Clin Infect Dis       Date:  2018-09-14       Impact factor: 9.079

2.  Epidemiological trends in HCV transmission and prevalence in the Viennese HIV+ population.

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  2 in total

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