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
  • [21] Remdesivir in treating hospitalized patients with COVID-19: A renewed review of clinical trials
    Wu, Zhenchao
    Han, Zhifei
    Liu, Beibei
    Shen, Ning
    FRONTIERS IN PHARMACOLOGY, 2022, 13
  • [22] Greek Remdesivir Cohort (GREC) Study: Effectiveness of Antiviral Drug Remdesivir in Hospitalized Patients with COVID-19 Pneumonia
    Petrakis, Vasilis
    Rapti, Vasiliki
    Akinosoglou, Karolina
    Bonelis, Constantinos
    Athanasiou, Kalomoira
    Dimakopoulou, Vasiliki
    Syrigos, Nikolaos K.
    Spernovasilis, Nikolaos
    Trypsianis, Grigoris
    Marangos, Markos
    Gogos, Charalambos
    Papazoglou, Dimitrios
    Panagopoulos, Periklis
    Poulakou, Garyfallia
    MICROORGANISMS, 2022, 10 (10)
  • [23] Remdesivir (GS-5734) in COVID-19 Therapy: The Fourth Chance
    Moirangthem, Dinesh S.
    Surbala, Laishram
    CURRENT DRUG TARGETS, 2021, 22 (12) : 1346 - 1356
  • [24] Remdesivir for Hospitalized COVID-19 Patients in the United States: Optimization of Health Care Resources
    Lianne Barnieh
    Rachel Beckerman
    Sushanth Jeyakumar
    Alice Hsiao
    James Jarrett
    Robert L. Gottlieb
    Infectious Diseases and Therapy, 2023, 12 : 1655 - 1665
  • [25] Remdesivir and GS-441524 Retain Antiviral Activity against Delta, Omicron, and Other Emergent SARS-CoV-2 Variants
    Pitts, Jared
    Li, Jiani
    Perry, Jason K.
    Du Pont, Venice
    Riola, Nicholas
    Rodriguez, Lauren
    Lu, Xianghan
    Kurhade, Chaitanya
    Xie, Xuping
    Camus, Gregory
    Manhas, Savrina
    Martin, Ross
    Shi, Pei-Yong
    Cihlar, Tomas
    Porter, Danielle P.
    Mo, Hongmei
    Maiorova, Evguenia
    Bilello, John P.
    ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2022, 66 (06)
  • [26] Remdesivir for Hospitalized COVID-19 Patients in the United States: Optimization of Health Care Resources
    Barnieh, Lianne
    Beckerman, Rachel
    Jeyakumar, Sushanth
    Hsiao, Alice
    Jarrett, James
    Gottlieb, Robert L.
    INFECTIOUS DISEASES AND THERAPY, 2023, 12 (06) : 1655 - 1665
  • [27] Cost-effectiveness of remdesivir for the treatment of hospitalized patients with COVID-19: a systematic review
    Rezapour, Aziz
    Behroozi, Zahra
    Nasirzadeh, Mostafa
    Rezaeian, Mohsen
    Barzegar, Mohammad
    Tashakori-Miyanroudi, Mahsa
    Sayyad, Abdollah
    Souresrafil, Aghdas
    INFECTIOUS DISEASES OF POVERTY, 2023, 12 (01)
  • [28] Cost-effectiveness of remdesivir for the treatment of hospitalized patients with COVID-19: a systematic review
    Aziz Rezapour
    Zahra Behroozi
    Mostafa Nasirzadeh
    Mohsen Rezaeian
    Mohammad Barzegar
    Mahsa Tashakori-Miyanroudi
    Abdollah Sayyad
    Aghdas Souresrafil
    Infectious Diseases of Poverty, 12
  • [29] Tocilizumab and remdesivir in hospitalized patients with severe COVID-19 pneumonia: a randomized clinical trial
    Rosas, Ivan O.
    Diaz, George
    Gottlieb, Robert L.
    Lobo, Suzana M.
    Robinson, Philip
    Hunter, Bradley D.
    Cavalcante, Adilson W.
    Overcash, J. Scott
    Hanania, Nicola A.
    Skarbnik, Alan
    Garcia-Diaz, Julia
    Gordeev, Ivan
    Carratala, Jordi
    Gordon, Oliver
    Graham, Emily
    Lewin-Koh, Nicholas
    Tsai, Larry
    Tuckwell, Katie
    Cao, Huyen
    Brainard, Diana
    Olsson, Julie K.
    INTENSIVE CARE MEDICINE, 2021, 47 (11) : 1258 - 1270
  • [30] Real-World Safety and Effectiveness of Remdesivir and Corticosteroids in Hospitalized Patients with COVID-19
    Caffrey, Aisling R.
    Liao, J. Xin
    Lopes, Vrishali V.
    LaPlante, Kerry L.
    Appaneal, Haley J.
    COVID, 2023, 3 (02): : 198 - 217