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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
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.
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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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