Population Pharmacokinetics of Remdesivir and GS-441524 in Hospitalized COVID-19 Patients

被引:13
|
作者
Leegwater, E. [1 ,2 ,3 ]
Moes, D. J. A. R. [4 ]
Bosma, L. B. E. [1 ]
Ottens, T. H. [5 ]
van der Meer, I. M. [6 ]
van Nieuwkoop, C. [6 ]
Wilms, E. B. [1 ,2 ]
机构
[1] Haga Teaching Hosp, Dept Hosp Pharm, The Hague, Netherlands
[2] Hague Hosp Pharm, The Hague, Netherlands
[3] Leiden Univ, Dept Infect Dis, Med Ctr, Leiden, Netherlands
[4] Leiden Univ, Dept Clin Pharm & Toxicol, Med Ctr, Leiden, Netherlands
[5] Haga Teaching Hosp, Dept Intens Care, The Hague, Netherlands
[6] Haga Teaching Hosp, Dept Internal Med, The Hague, Netherlands
关键词
COVID-19; pharmacokinetics; remdesivir;
D O I
10.1128/aac.00254-22
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The objective of this study was to describe the population pharmacokinetics of remdesivir and GS-441524 in hospitalized coronavirus disease 2019 (COVID-19) patients. A prospective observational pharmacokinetic study was performed in non-critically ill hospitalized COVID-19 patients with hypoxemia. For evaluation of the plasma concentrations of remdesivir and its metabolite GS-441524, samples were collected on the first day of therapy. A nonlinear mixed-effects model was developed to describe the pharmacokinetics and identify potential covariates that explain variability. Alternative dosing regimens were evaluated using Monte Carlo simulations. Seventeen patients were included. Remdesivir and GS-441524 pharmacokinetics were best described by a one-compartment model. The estimated glomerular filtration rate (eGFR) on GS-441524 clearance was identified as a clinically relevant covariate. The interindividual variability in clearance and volume of distribution for both remdesivir and GS-441524 was high (remdesivir, 38.9% and 47.9%, respectively; GS-441525, 47.4% and 42.9%, respectively). The estimated elimination half-life for remdesivir was 0.48 h, and that for GS-441524 was 26.6 h. The probability of target attainment (PTA) of the in vitro 50% effective concentration (EC50) for GS-441524 in plasma can be improved by shortening the dose interval of remdesivir and thereby increasing the total daily dose (PTA, 51.4% versus 94.7%). In patients with reduced renal function, the metabolite GS-441524 accumulates. A population pharmacokinetic model for remdesivir and GS-441524 in COVID-19 patients was developed. Remdesivir showed highly variable pharmacokinetics. The elimination half-life of remdesivir in COVID-19 patients is short, and the clearance of GS-441524 is dependent on the eGFR. Alternative dosing regimens aimed at optimizing the remdesivir and GS-441524 concentrations may improve the effectiveness of remdesivir treatment in COVID-19 patients.
引用
收藏
页数:10
相关论文
共 50 条
  • [41] Can remdesivir and its parent nucleoside GS-441524 be potential oral drugs? An in vitro and in vivo DMPK assessment
    Xie, Jiashu
    Wang, Zhengqiang
    ACTA PHARMACEUTICA SINICA B, 2021, 11 (06) : 1607 - 1616
  • [42] Real-life use of remdesivir in hospitalized patients with COVID-19
    Garcia-Vidal, Carolina
    Meira, Fernanda
    Duenas, Gerard
    Puerta-Alcalde, Pedro
    Garcia-Pouton, Nicole
    Chumbita, Mariana
    Cardozo, Celia
    Hernandez-Meneses, Marta
    Alonso-Navarro, Rodrigo
    Rico, Veronica
    Aguero, Daiana
    Bodro, Marta
    Morata, Laura
    Jordan, Carlota
    Lopera, Carlos
    Ambrosioni, Juan
    Segui, Ferran
    Grafia, Nacho
    Castro, Pedro
    Garcia, Felipe
    Mensa, Josep
    Martinez, Jose Antonio
    Sanjuan, Gemma
    Soriano, Alex
    Cozar-Llisto, Alberto
    REVISTA ESPANOLA DE QUIMIOTERAPIA, 2021, 34 (02) : 136 - 140
  • [43] The effect of remdesivir for the treatment of COVID-19 on mortality among hospitalized patients
    Breskin, Alexander
    Wiener, Catherine
    Brookhart, M. Alan
    PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2022, 31 : 96 - 96
  • [44] Remdesivir for patients with COVID-19
    Wu, Peter E.
    Morris, Andrew M.
    CANADIAN MEDICAL ASSOCIATION JOURNAL, 2021, 193 (04) : E125 - E125
  • [45] Remdesivir for patients with COVID-19
    Wu, Peter E.
    Morris, Andrew M.
    CANADIAN MEDICAL ASSOCIATION JOURNAL, 2021, 193 (14) : E495 - E496
  • [46] Remdesivir for Patients with COVID-19
    Augustin, M.
    Hallek, M.
    Nitschmann, S.
    INTERNIST, 2020, 61 (08): : 869 - 872
  • [47] Can remdesivir and its parent nucleoside GS-441524 be potential oral drugs? An in vitro and in vivo DMPK assessment
    Jiashu Xie
    Zhengqiang Wang
    Acta Pharmaceutica Sinica B, 2021, 11 (06) : 1607 - 1616
  • [48] Structural Insights into Plasticity and Discovery of Remdesivir Metabolite GS-441524 Binding in SARS-CoV-2 Macrodomain
    Ni, Xiaomin
    Schroeder, Martin
    Olieric, Vincent
    Sharpe, May E.
    Hernandez-Olmos, Victor
    Proschak, Ewgenij
    Merk, Daniel
    Knapp, Stefan
    Chaikuad, Apirat
    ACS MEDICINAL CHEMISTRY LETTERS, 2021, 12 (04): : 603 - 609
  • [49] Pharmacokinetics and pharmacodynamics of hydroxychloroquine in hospitalized patients with COVID-19
    Zahr, Noel
    Urien, Saik
    Llopis, Benoit
    Pourcher, Valerie
    Paccoud, Olivier
    Bleibtreu, Alexandre
    Mayaux, Julien
    Gandjbakhch, Estelle
    Hekimian, Guillaume
    Combes, Alain
    Benveniste, Olivier
    Saadoun, David
    Allenbach, Yves
    Pinna, Bruno
    Cacoub, Patrice
    Funck-Brentano, Christian
    Salem, Joe-Elie
    THERAPIE, 2021, 76 (04): : 285 - 295
  • [50] Baricitinib plus Remdesivir for Hospitalized Adults with Covid-19
    Andre C Kalil
    四川生理科学杂志, 2020, 42 (04) : 451 - 451