Physiologically‐based pharmacokinetic modelling guided dose evaluations of nirmatrelvir/ritonavir in renal impairment for the management of COVID‐19

We aimed to address factors contributing to the pharmacokinetic changes of nirmatrelvir/ritonavir in renal impaired (RI) patients and recommend dosing adjustment via a physiologically‐based pharmacokinetic (PBPK) modelling approach. A PBPK model of nirmatrelvir/ritonavir was developed via Simcyp® Si...

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Published inBritish journal of clinical pharmacology Vol. 91; no. 4; pp. 1041 - 1048
Main Authors Ng, Tat Ming, Wang, Ziteng, Chan, Eric Chun Yong
Format Journal Article
LanguageEnglish
Published England 01.04.2025
Subjects
Online AccessGet full text
ISSN0306-5251
1365-2125
1365-2125
DOI10.1111/bcp.16074

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Abstract We aimed to address factors contributing to the pharmacokinetic changes of nirmatrelvir/ritonavir in renal impaired (RI) patients and recommend dosing adjustment via a physiologically‐based pharmacokinetic (PBPK) modelling approach. A PBPK model of nirmatrelvir/ritonavir was developed via Simcyp® Simulator. Sensitivity analysis of the influence of hepatic CYP3A4 intrinsic clearance and abundance, as well as hepatic non‐CYP3A4 metabolism (other human liver microsomes [HLM] CLint) was performed to evaluate the effects of RI on oral clearance of nirmatrelvir. Other HLM CLint, the most sensitive parameter, was adjusted, and the simulated plasma concentration profiles of nirmatrelvir in severe RI subjects were within the therapeutic index of 292–10 000 ng/mL for dosing regimens of loading doses of 300/100 mg followed by 150/100 mg or 75/100 mg twice daily of nirmatrelvir/ritonavir. Considering that nirmatrelvir is available as a 150 mg tablet, we recommend 300/100 mg followed by 150/100 mg twice daily as the dosing regimen to be investigated in severe RI.
AbstractList We aimed to address factors contributing to the pharmacokinetic changes of nirmatrelvir/ritonavir in renal impaired (RI) patients and recommend dosing adjustment via a physiologically‐based pharmacokinetic (PBPK) modelling approach. A PBPK model of nirmatrelvir/ritonavir was developed via Simcyp® Simulator. Sensitivity analysis of the influence of hepatic CYP3A4 intrinsic clearance and abundance, as well as hepatic non‐CYP3A4 metabolism (other human liver microsomes [HLM] CLint) was performed to evaluate the effects of RI on oral clearance of nirmatrelvir. Other HLM CLint, the most sensitive parameter, was adjusted, and the simulated plasma concentration profiles of nirmatrelvir in severe RI subjects were within the therapeutic index of 292–10 000 ng/mL for dosing regimens of loading doses of 300/100 mg followed by 150/100 mg or 75/100 mg twice daily of nirmatrelvir/ritonavir. Considering that nirmatrelvir is available as a 150 mg tablet, we recommend 300/100 mg followed by 150/100 mg twice daily as the dosing regimen to be investigated in severe RI.
We aimed to address factors contributing to the pharmacokinetic changes of nirmatrelvir/ritonavir in renal impaired (RI) patients and recommend dosing adjustment via a physiologically-based pharmacokinetic (PBPK) modelling approach. A PBPK model of nirmatrelvir/ritonavir was developed via Simcyp® Simulator. Sensitivity analysis of the influence of hepatic CYP3A4 intrinsic clearance and abundance, as well as hepatic non-CYP3A4 metabolism (other human liver microsomes [HLM] CL ) was performed to evaluate the effects of RI on oral clearance of nirmatrelvir. Other HLM CL , the most sensitive parameter, was adjusted, and the simulated plasma concentration profiles of nirmatrelvir in severe RI subjects were within the therapeutic index of 292-10 000 ng/mL for dosing regimens of loading doses of 300/100 mg followed by 150/100 mg or 75/100 mg twice daily of nirmatrelvir/ritonavir. Considering that nirmatrelvir is available as a 150 mg tablet, we recommend 300/100 mg followed by 150/100 mg twice daily as the dosing regimen to be investigated in severe RI.
We aimed to address factors contributing to the pharmacokinetic changes of nirmatrelvir/ritonavir in renal impaired (RI) patients and recommend dosing adjustment via a physiologically‐based pharmacokinetic (PBPK) modelling approach. A PBPK model of nirmatrelvir/ritonavir was developed via Simcyp® Simulator. Sensitivity analysis of the influence of hepatic CYP3A4 intrinsic clearance and abundance, as well as hepatic non‐CYP3A4 metabolism (other human liver microsomes [HLM] CL int ) was performed to evaluate the effects of RI on oral clearance of nirmatrelvir. Other HLM CL int , the most sensitive parameter, was adjusted, and the simulated plasma concentration profiles of nirmatrelvir in severe RI subjects were within the therapeutic index of 292–10 000 ng/mL for dosing regimens of loading doses of 300/100 mg followed by 150/100 mg or 75/100 mg twice daily of nirmatrelvir/ritonavir. Considering that nirmatrelvir is available as a 150 mg tablet, we recommend 300/100 mg followed by 150/100 mg twice daily as the dosing regimen to be investigated in severe RI.
We aimed to address factors contributing to the pharmacokinetic changes of nirmatrelvir/ritonavir in renal impaired (RI) patients and recommend dosing adjustment via a physiologically-based pharmacokinetic (PBPK) modelling approach. A PBPK model of nirmatrelvir/ritonavir was developed via Simcyp® Simulator. Sensitivity analysis of the influence of hepatic CYP3A4 intrinsic clearance and abundance, as well as hepatic non-CYP3A4 metabolism (other human liver microsomes [HLM] CLint) was performed to evaluate the effects of RI on oral clearance of nirmatrelvir. Other HLM CLint, the most sensitive parameter, was adjusted, and the simulated plasma concentration profiles of nirmatrelvir in severe RI subjects were within the therapeutic index of 292-10 000 ng/mL for dosing regimens of loading doses of 300/100 mg followed by 150/100 mg or 75/100 mg twice daily of nirmatrelvir/ritonavir. Considering that nirmatrelvir is available as a 150 mg tablet, we recommend 300/100 mg followed by 150/100 mg twice daily as the dosing regimen to be investigated in severe RI.We aimed to address factors contributing to the pharmacokinetic changes of nirmatrelvir/ritonavir in renal impaired (RI) patients and recommend dosing adjustment via a physiologically-based pharmacokinetic (PBPK) modelling approach. A PBPK model of nirmatrelvir/ritonavir was developed via Simcyp® Simulator. Sensitivity analysis of the influence of hepatic CYP3A4 intrinsic clearance and abundance, as well as hepatic non-CYP3A4 metabolism (other human liver microsomes [HLM] CLint) was performed to evaluate the effects of RI on oral clearance of nirmatrelvir. Other HLM CLint, the most sensitive parameter, was adjusted, and the simulated plasma concentration profiles of nirmatrelvir in severe RI subjects were within the therapeutic index of 292-10 000 ng/mL for dosing regimens of loading doses of 300/100 mg followed by 150/100 mg or 75/100 mg twice daily of nirmatrelvir/ritonavir. Considering that nirmatrelvir is available as a 150 mg tablet, we recommend 300/100 mg followed by 150/100 mg twice daily as the dosing regimen to be investigated in severe RI.
Author Ng, Tat Ming
Wang, Ziteng
Chan, Eric Chun Yong
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Cites_doi 10.1016/j.bcp.2014.06.020
10.1093/cid/ciad785
10.1093/toxsci/kfp255
10.2165/00003088‐199835040‐00002
10.1124/dmd.114.058099
10.1038/s41374‐021‐00610‐9
10.1128/aac.01229‐22
10.1016/j.xphs.2023.09.028
10.23876/j.krcp.22.194
10.1002/cpt.2683
10.1016/j.ijantimicag.2023.106997
10.1001/jamanetworkopen.2022.29236
10.1126/science.abl4784
10.1208/s12248‐014‐9626‐3
10.1007/s11095‐023‐03538‐5
10.1124/dmd.115.065920
10.1038/ki.2013.399
10.1002/cpt.2688
10.1002/cpt.2603
10.1002/cpt.337
10.2215/CJN.0000000000000107
10.1016/j.cmpb.2010.01.007
10.1124/dmd.110.036103
10.1124/dmd.112.045302
10.1124/dmd.121.000801
10.1016/S0140‐6736(22)01586‐0
10.1586/ecp.10.143
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Issue 4
Keywords nirmatrelvir/ritonavir
COVID‐19
severe renal impairment
dosing adjustment recommendation
physiologically‐based pharmacokinetic model
Language English
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2024 British Pharmacological Society.
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Notes Funding information
Tat Ming Ng and Ziteng Wang are joint first authors.
Part of this work was supported by the Joseph Lim Boon Tiong Urology Cancer Research (A‐0002678‐01‐00) provided to Eric Chun Yong Chan and the NMRC research training fellowship (MOH‐RTF21nov‐0005) provided to Tat Ming Ng.
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References 2022; 112
2010; 99
2014; 91
2023; 18
2021; 101
2022; 50
2016; 100
2009; 113
2022; 66
2014; 85
2011; 4
2011; 39
2014; 42
2023; 42
2023; 40
2023
2022; 5
2015; 43
2014; 16
2024; 63
2024; 113
2021; 374
2022; 400
1998; 35
2012; 40
e_1_2_8_28_1
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e_1_2_8_25_1
e_1_2_8_26_1
e_1_2_8_27_1
e_1_2_8_3_1
e_1_2_8_2_1
e_1_2_8_5_1
e_1_2_8_4_1
e_1_2_8_7_1
e_1_2_8_6_1
e_1_2_8_9_1
e_1_2_8_8_1
e_1_2_8_20_1
e_1_2_8_21_1
e_1_2_8_22_1
e_1_2_8_23_1
e_1_2_8_17_1
e_1_2_8_18_1
e_1_2_8_19_1
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e_1_2_8_14_1
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e_1_2_8_16_1
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References_xml – volume: 112
  start-page: 1201
  issue: 6
  year: 2022
  end-page: 1206
  article-title: Metabolism and excretion of nirmatrelvir in humans using quantitative fluorine nuclear magnetic resonance spectroscopy: a novel approach for accelerating drug development
  publication-title: Clin Pharmacol Ther
– volume: 63
  issue: 1
  year: 2024
  article-title: High concentrations of nirmatrelvir/ritonavir in critically ill patients receiving continuous renal replacement therapy
  publication-title: Int J Antimicrob Agents
– volume: 35
  start-page: 275
  issue: 4
  year: 1998
  end-page: 291
  article-title: Ritonavir: clinical pharmacokinetics and interactions with other anti‐HIV agents
  publication-title: Clin Pharmacokinet
– volume: 40
  start-page: 1686
  issue: 9
  year: 2012
  end-page: 1697
  article-title: Selective mechanism‐based inactivation of CYP3A4 by CYP3cide (PF‐04981517) and its utility as an in vitro tool for delineating the relative roles of CYP3A4 versus CYP3A5 in the metabolism of drugs
  publication-title: Drug Metab Dispos
– volume: 66
  issue: 11
  year: 2022
  article-title: Pharmacokinetics of nirmatrelvir and ritonavir in COVID‐19 patients with end‐stage renal disease on intermittent hemodialysis
  publication-title: Antimicrob Agents Chemother
– year: 2023
  article-title: Nirmatrelvir and ritonavir combination in COVID‐19 patients with advanced chronic kidney disease
  publication-title: Clin Infect Dis
– volume: 5
  start-page: e2229236
  issue: 8
  year: 2022
  end-page: e2229236
  article-title: Remdesivir in patients with severe kidney dysfunction: a secondary analysis of the CATCO randomized trial
  publication-title: JAMA Netw Open
– volume: 18
  start-page: 485
  issue: 4
  year: 2023
  end-page: 490
  article-title: Early experience with modified dose nirmatrelvir/ritonavir in dialysis patients with coronavirus disease 2019
  publication-title: Clin J Am Soc Nephrol
– volume: 101
  start-page: 1197
  issue: 9
  year: 2021
  end-page: 1209
  article-title: Advanced oxidation protein products downregulate CYP1A2 and CYP3A4 expression and activity via the NF‐κB‐mediated signaling pathway in vitro and in vivo
  publication-title: Lab Invest
– volume: 113
  start-page: 64
  issue: 1
  year: 2024
  end-page: 71
  article-title: PBPK modeling of PAXLOVIDTM: incorporating rotamer conversion kinetics to advanced dissolution and absorption model
  publication-title: J Pharm Sci
– volume: 91
  start-page: 109
  issue: 1
  year: 2014
  end-page: 118
  article-title: Investigating the contribution of CYP2J2 to ritonavir metabolism in vitro and in vivo
  publication-title: Biochem Pharmacol
– volume: 16
  start-page: 1018
  issue: 5
  year: 2014
  end-page: 1028
  article-title: Application of a physiologically based pharmacokinetic model informed by a top‐down approach for the prediction of pharmacokinetics in chronic kidney disease patients
  publication-title: AAPS J
– volume: 43
  start-page: 1823
  issue: 11
  year: 2015
  end-page: 1837
  article-title: Physiologically based pharmacokinetic (PBPK) modeling and simulation approaches: a systematic review of published models, applications, and model verification
  publication-title: Drug Metab Dispos
– volume: 100
  start-page: 75
  issue: 1
  year: 2016
  end-page: 87
  article-title: Systematic and quantitative assessment of the effect of chronic kidney disease on CYP2D6 and CYP3A4/5
  publication-title: Clin Pharmacol Ther
– volume: 400
  start-page: 1213
  issue: 10359
  year: 2022
  end-page: 1222
  article-title: Real‐world effectiveness of molnupiravir and nirmatrelvir plus ritonavir against mortality, hospitalisation, and in‐hospital outcomes among community‐dwelling, ambulatory patients with confirmed SARS‐CoV‐2 infection during the omicron wave in Hong Kong: an observational study
  publication-title: Lancet
– volume: 99
  start-page: 306
  issue: 3
  year: 2010
  end-page: 314
  article-title: PKSolver: an add‐in program for pharmacokinetic and pharmacodynamic data analysis in Microsoft Excel
  publication-title: Comput Methods Programs Biomed
– volume: 4
  start-page: 261
  issue: 2
  year: 2011
  end-page: 274
  article-title: Modeling and predicting drug pharmacokinetics in patients with renal impairment
  publication-title: Expert Rev Clin Pharmacol
– volume: 85
  start-page: 522
  issue: 3
  year: 2014
  end-page: 528
  article-title: Effects of chronic kidney disease and uremia on hepatic drug metabolism and transport
  publication-title: Kidney Int
– volume: 50
  start-page: 576
  issue: 5
  year: 2022
  end-page: 590
  article-title: Disposition of nirmatrelvir, an orally bioavailable inhibitor of SARS‐CoV‐2 3C‐like protease, across animals and humans
  publication-title: Drug Metab Dispos
– volume: 113
  start-page: 293
  issue: 2
  year: 2009
  end-page: 304
  article-title: Effects of cytochrome P450 inhibitors on the biotransformation of fluorogenic substrates by adult male rat liver microsomes and cDNA‐expressed rat cytochrome P450 isoforms
  publication-title: Toxicol Sci
– volume: 42
  start-page: 275
  issue: 2
  year: 2023
  end-page: 278
  article-title: Safety and efficiency of molnupiravir for COVID‐19 patients with advanced chronic kidney disease
  publication-title: Kidney Res Clin Pract
– volume: 40
  start-page: 1927
  issue: 8
  year: 2023
  end-page: 1938
  article-title: Physiologically‐based pharmacokinetic modeling of PAXLOVID™ with first‐order absorption kinetics
  publication-title: Pharm Res
– volume: 42
  start-page: 1478
  issue: 9
  year: 2014
  end-page: 1484
  article-title: Deciding on success criteria for predictability of pharmacokinetic parameters from in vitro studies: an analysis based on in vivo observations
  publication-title: Drug Metab Dispos
– volume: 374
  start-page: 1586
  issue: 6575
  year: 2021
  end-page: 1593
  article-title: An oral SARS‐CoV‐2 M (pro) inhibitor clinical candidate for the treatment of COVID‐19
  publication-title: Science
– volume: 39
  start-page: 170
  issue: 2
  year: 2011
  end-page: 173
  article-title: Critique of the two‐fold measure of prediction success for ratios: application for the assessment of drug‐drug interactions
  publication-title: Drug Metab Dispos
– volume: 112
  start-page: 101
  issue: 1
  year: 2022
  end-page: 111
  article-title: Innovative randomized phase I study and dosing regimen selection to accelerate and inform pivotal COVID‐19 trial of nirmatrelvir
  publication-title: Clin Pharmacol Ther
– volume: 112
  start-page: 892
  issue: 4
  year: 2022
  end-page: 900
  article-title: Pharmacokinetics of oral nirmatrelvir/ritonavir, a protease inhibitor for treatment of COVID‐19, in subjects with renal impairment
  publication-title: Clin Pharmacol Ther
– ident: e_1_2_8_29_1
  doi: 10.1016/j.bcp.2014.06.020
– ident: e_1_2_8_14_1
  doi: 10.1093/cid/ciad785
– ident: e_1_2_8_27_1
  doi: 10.1093/toxsci/kfp255
– ident: e_1_2_8_5_1
  doi: 10.2165/00003088‐199835040‐00002
– ident: e_1_2_8_21_1
  doi: 10.1124/dmd.114.058099
– ident: e_1_2_8_25_1
  doi: 10.1038/s41374‐021‐00610‐9
– ident: e_1_2_8_3_1
– ident: e_1_2_8_31_1
  doi: 10.1128/aac.01229‐22
– ident: e_1_2_8_22_1
– ident: e_1_2_8_19_1
  doi: 10.1016/j.xphs.2023.09.028
– ident: e_1_2_8_9_1
  doi: 10.23876/j.krcp.22.194
– ident: e_1_2_8_7_1
  doi: 10.1002/cpt.2683
– ident: e_1_2_8_13_1
  doi: 10.1016/j.ijantimicag.2023.106997
– ident: e_1_2_8_2_1
– ident: e_1_2_8_10_1
  doi: 10.1001/jamanetworkopen.2022.29236
– ident: e_1_2_8_16_1
  doi: 10.1126/science.abl4784
– ident: e_1_2_8_23_1
  doi: 10.1208/s12248‐014‐9626‐3
– ident: e_1_2_8_15_1
  doi: 10.1007/s11095‐023‐03538‐5
– ident: e_1_2_8_20_1
  doi: 10.1124/dmd.115.065920
– ident: e_1_2_8_24_1
  doi: 10.1038/ki.2013.399
– ident: e_1_2_8_12_1
  doi: 10.1002/cpt.2688
– ident: e_1_2_8_17_1
  doi: 10.1002/cpt.2603
– ident: e_1_2_8_8_1
– ident: e_1_2_8_30_1
  doi: 10.1002/cpt.337
– ident: e_1_2_8_11_1
  doi: 10.2215/CJN.0000000000000107
– ident: e_1_2_8_18_1
  doi: 10.1016/j.cmpb.2010.01.007
– ident: e_1_2_8_32_1
  doi: 10.1124/dmd.110.036103
– ident: e_1_2_8_28_1
  doi: 10.1124/dmd.112.045302
– ident: e_1_2_8_6_1
  doi: 10.1124/dmd.121.000801
– ident: e_1_2_8_4_1
  doi: 10.1016/S0140‐6736(22)01586‐0
– ident: e_1_2_8_26_1
  doi: 10.1586/ecp.10.143
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Snippet We aimed to address factors contributing to the pharmacokinetic changes of nirmatrelvir/ritonavir in renal impaired (RI) patients and recommend dosing...
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SubjectTerms Antiviral Agents - administration & dosage
Antiviral Agents - pharmacokinetics
COVID-19 Drug Treatment
COVID‐19
Cytochrome P-450 CYP3A - metabolism
Dose-Response Relationship, Drug
dosing adjustment recommendation
Drug Combinations
Female
Humans
Male
Microsomes, Liver - metabolism
Middle Aged
Models, Biological
nirmatrelvir/ritonavir
physiologically‐based pharmacokinetic model
Renal Insufficiency - complications
Renal Insufficiency - metabolism
Ritonavir - administration & dosage
Ritonavir - pharmacokinetics
severe renal impairment
Title Physiologically‐based pharmacokinetic modelling guided dose evaluations of nirmatrelvir/ritonavir in renal impairment for the management of COVID‐19
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fbcp.16074
https://www.ncbi.nlm.nih.gov/pubmed/38616514
https://www.proquest.com/docview/3039235367
Volume 91
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