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 in | British journal of clinical pharmacology Vol. 91; no. 4; pp. 1041 - 1048 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
England
01.04.2025
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Subjects | |
Online Access | Get full text |
ISSN | 0306-5251 1365-2125 1365-2125 |
DOI | 10.1111/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. |
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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 |
Author_xml | – sequence: 1 givenname: Tat Ming orcidid: 0000-0002-4570-3266 surname: Ng fullname: Ng, Tat Ming email: tat_ming_ng@ttsh.com.sg organization: Tan Tock Seng Hospital – sequence: 2 givenname: Ziteng orcidid: 0000-0001-7352-9683 surname: Wang fullname: Wang, Ziteng organization: National University of Singapore – sequence: 3 givenname: Eric Chun Yong orcidid: 0000-0001-6107-9072 surname: Chan fullname: Chan, Eric Chun Yong email: phaccye@nus.edu.sg organization: National University of Singapore |
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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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Keywords | nirmatrelvir/ritonavir COVID‐19 severe renal impairment dosing adjustment recommendation physiologically‐based pharmacokinetic model |
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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. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
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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 |
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