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No Pharmacokinetic Interactions Between Elbasvir or Grazoprevir and Methadone in Participants Receiving Maintenance Opioid Agonist Therapy
We conducted two phase I trials to evaluate the pharmacokinetic interactions between elbasvir (EBR), grazoprevir (GZR), and methadone (MK‐8742‐P010 and MK‐5172‐P030) in non‐hepatitis C virus (HCV)‐infected participants on methadone maintenance therapy. Coadministration of EBR or GZR with methadone h...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6226122/ https://www.ncbi.nlm.nih.gov/pubmed/30040872 http://dx.doi.org/10.1111/cts.12564 |
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author | Feng, Hwa‐Ping Guo, Zifang Caro, Luzelena Marshall, William L. Liu, Fang Panebianco, Deborah Vaddady, Pavan Reitmann, Christina Jumes, Patricia Wolford, Dennis Fraser, Iain Valesky, Robert Martinho, Monika Butterton, Joan R. Iwamoto, Marian Webster, Lynn Yeh, Wendy W. |
author_facet | Feng, Hwa‐Ping Guo, Zifang Caro, Luzelena Marshall, William L. Liu, Fang Panebianco, Deborah Vaddady, Pavan Reitmann, Christina Jumes, Patricia Wolford, Dennis Fraser, Iain Valesky, Robert Martinho, Monika Butterton, Joan R. Iwamoto, Marian Webster, Lynn Yeh, Wendy W. |
author_sort | Feng, Hwa‐Ping |
collection | PubMed |
description | We conducted two phase I trials to evaluate the pharmacokinetic interactions between elbasvir (EBR), grazoprevir (GZR), and methadone (MK‐8742‐P010 and MK‐5172‐P030) in non‐hepatitis C virus (HCV)‐infected participants on methadone maintenance therapy. Coadministration of EBR or GZR with methadone had no clinically meaningful effect on EBR, GZR, or methadone pharmacokinetics. The geometric mean ratios (GMRs) for R‐ and S‐methadone AUC(0‐24) were 1.03 (90% confidence interval (CI), 0.92–1.15) and 1.09 (90% CI, 0.94–1.26) in the presence/absence of EBR; and 1.09 (90% CI, 1.02–1.17) and 1.23 (90% CI, 1.12–1.35) in the presence/absence of GZR. The GMRs for EBR and GZR AUC(0‐24) in participants receiving methadone relative to a healthy historical cohort not receiving methadone were 1.20 (90% CI, 0.94–1.53) and 1.03 (90% CI, 0.76–1.41), respectively. These results indicate that no dose adjustment is required for individuals with HCV infection receiving stable methadone therapy and the EBR/GZR fixed‐dose regimen. |
format | Online Article Text |
id | pubmed-6226122 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62261222018-11-19 No Pharmacokinetic Interactions Between Elbasvir or Grazoprevir and Methadone in Participants Receiving Maintenance Opioid Agonist Therapy Feng, Hwa‐Ping Guo, Zifang Caro, Luzelena Marshall, William L. Liu, Fang Panebianco, Deborah Vaddady, Pavan Reitmann, Christina Jumes, Patricia Wolford, Dennis Fraser, Iain Valesky, Robert Martinho, Monika Butterton, Joan R. Iwamoto, Marian Webster, Lynn Yeh, Wendy W. Clin Transl Sci Research We conducted two phase I trials to evaluate the pharmacokinetic interactions between elbasvir (EBR), grazoprevir (GZR), and methadone (MK‐8742‐P010 and MK‐5172‐P030) in non‐hepatitis C virus (HCV)‐infected participants on methadone maintenance therapy. Coadministration of EBR or GZR with methadone had no clinically meaningful effect on EBR, GZR, or methadone pharmacokinetics. The geometric mean ratios (GMRs) for R‐ and S‐methadone AUC(0‐24) were 1.03 (90% confidence interval (CI), 0.92–1.15) and 1.09 (90% CI, 0.94–1.26) in the presence/absence of EBR; and 1.09 (90% CI, 1.02–1.17) and 1.23 (90% CI, 1.12–1.35) in the presence/absence of GZR. The GMRs for EBR and GZR AUC(0‐24) in participants receiving methadone relative to a healthy historical cohort not receiving methadone were 1.20 (90% CI, 0.94–1.53) and 1.03 (90% CI, 0.76–1.41), respectively. These results indicate that no dose adjustment is required for individuals with HCV infection receiving stable methadone therapy and the EBR/GZR fixed‐dose regimen. John Wiley and Sons Inc. 2018-07-24 2018-11 /pmc/articles/PMC6226122/ /pubmed/30040872 http://dx.doi.org/10.1111/cts.12564 Text en © 2018 The Authors. Clinical and Translational Science published by Wiley Periodicals, Inc. on behalf of American Society for Clinical Pharmacology and Therapeutics This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Feng, Hwa‐Ping Guo, Zifang Caro, Luzelena Marshall, William L. Liu, Fang Panebianco, Deborah Vaddady, Pavan Reitmann, Christina Jumes, Patricia Wolford, Dennis Fraser, Iain Valesky, Robert Martinho, Monika Butterton, Joan R. Iwamoto, Marian Webster, Lynn Yeh, Wendy W. No Pharmacokinetic Interactions Between Elbasvir or Grazoprevir and Methadone in Participants Receiving Maintenance Opioid Agonist Therapy |
title | No Pharmacokinetic Interactions Between Elbasvir or Grazoprevir and Methadone in Participants Receiving Maintenance Opioid Agonist Therapy |
title_full | No Pharmacokinetic Interactions Between Elbasvir or Grazoprevir and Methadone in Participants Receiving Maintenance Opioid Agonist Therapy |
title_fullStr | No Pharmacokinetic Interactions Between Elbasvir or Grazoprevir and Methadone in Participants Receiving Maintenance Opioid Agonist Therapy |
title_full_unstemmed | No Pharmacokinetic Interactions Between Elbasvir or Grazoprevir and Methadone in Participants Receiving Maintenance Opioid Agonist Therapy |
title_short | No Pharmacokinetic Interactions Between Elbasvir or Grazoprevir and Methadone in Participants Receiving Maintenance Opioid Agonist Therapy |
title_sort | no pharmacokinetic interactions between elbasvir or grazoprevir and methadone in participants receiving maintenance opioid agonist therapy |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6226122/ https://www.ncbi.nlm.nih.gov/pubmed/30040872 http://dx.doi.org/10.1111/cts.12564 |
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