Cargando…

Population Pharmacokinetic Analyses for Plazomicin Using Pooled Data from Phase 1, 2, and 3 Clinical Studies

Plazomicin is an aminoglycoside with activity against multidrug-resistant Enterobacteriaceae. Plazomicin is dosed on a milligram-per-kilogram-of-body-weight basis and administered by a 30-min intravenous infusion every 24 h, with dose adjustments being made for renal impairment and a body weight (BW...

Descripción completa

Detalles Bibliográficos
Autores principales: Trang, Michael, Seroogy, Julie D., Van Wart, Scott A., Bhavnani, Sujata M., Kim, Aryun, Gibbons, Jacqueline A., Ambrose, Paul G., Rubino, Christopher M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6496156/
https://www.ncbi.nlm.nih.gov/pubmed/30670433
http://dx.doi.org/10.1128/AAC.02329-18
_version_ 1783415385091997696
author Trang, Michael
Seroogy, Julie D.
Van Wart, Scott A.
Bhavnani, Sujata M.
Kim, Aryun
Gibbons, Jacqueline A.
Ambrose, Paul G.
Rubino, Christopher M.
author_facet Trang, Michael
Seroogy, Julie D.
Van Wart, Scott A.
Bhavnani, Sujata M.
Kim, Aryun
Gibbons, Jacqueline A.
Ambrose, Paul G.
Rubino, Christopher M.
author_sort Trang, Michael
collection PubMed
description Plazomicin is an aminoglycoside with activity against multidrug-resistant Enterobacteriaceae. Plazomicin is dosed on a milligram-per-kilogram-of-body-weight basis and administered by a 30-min intravenous infusion every 24 h, with dose adjustments being made for renal impairment and a body weight (BW) of ≥125% of ideal BW. A population pharmacokinetic analysis was performed to identify patient factors that account for variability in pharmacokinetics and to determine if dose adjustments are warranted based on covariates. The analysis included 143 healthy adults and 421 adults with complicated urinary tract infection (cUTI), acute pyelonephritis, bloodstream infection, or hospital-acquired bacterial pneumonia/ventilator-associated bacterial pneumonia (HABP/VABP) from seven studies (phases 1 to 3). A three-compartment structural pharmacokinetic model with a zero-order rate constant for the intravenous infusion and linear first-order elimination kinetics best described the plasma concentration-time profiles. The base structural model included creatinine clearance (CL(CR)) as a time-varying covariate for clearance. The covariates included age, BW, height, body surface area, body mass index, sex, race, and disease-related factors. The ranges of the α-, β-, and γ-phase half-lives for the analysis population were 0.328 to 1.58, 2.77 to 5.38, and 25.8 to 36.5 h, respectively. Total and renal clearances in a typical cUTI or HABP/VABP patient were 4.57 and 4.08 liters/h, respectively. Starting dose adjustments for CL(CR) are sufficient for minimizing the variation in plasma exposure across patient populations; adjustments based on other covariates are not warranted. The results support initial dosing on a milligram-per-kilogram basis with adjustments for CL(CR) and BW. Subsequent adjustments based on therapeutic drug management are recommended in certain subsets of patients, including the critically ill and renally impaired.
format Online
Article
Text
id pubmed-6496156
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-64961562019-06-03 Population Pharmacokinetic Analyses for Plazomicin Using Pooled Data from Phase 1, 2, and 3 Clinical Studies Trang, Michael Seroogy, Julie D. Van Wart, Scott A. Bhavnani, Sujata M. Kim, Aryun Gibbons, Jacqueline A. Ambrose, Paul G. Rubino, Christopher M. Antimicrob Agents Chemother Pharmacology Plazomicin is an aminoglycoside with activity against multidrug-resistant Enterobacteriaceae. Plazomicin is dosed on a milligram-per-kilogram-of-body-weight basis and administered by a 30-min intravenous infusion every 24 h, with dose adjustments being made for renal impairment and a body weight (BW) of ≥125% of ideal BW. A population pharmacokinetic analysis was performed to identify patient factors that account for variability in pharmacokinetics and to determine if dose adjustments are warranted based on covariates. The analysis included 143 healthy adults and 421 adults with complicated urinary tract infection (cUTI), acute pyelonephritis, bloodstream infection, or hospital-acquired bacterial pneumonia/ventilator-associated bacterial pneumonia (HABP/VABP) from seven studies (phases 1 to 3). A three-compartment structural pharmacokinetic model with a zero-order rate constant for the intravenous infusion and linear first-order elimination kinetics best described the plasma concentration-time profiles. The base structural model included creatinine clearance (CL(CR)) as a time-varying covariate for clearance. The covariates included age, BW, height, body surface area, body mass index, sex, race, and disease-related factors. The ranges of the α-, β-, and γ-phase half-lives for the analysis population were 0.328 to 1.58, 2.77 to 5.38, and 25.8 to 36.5 h, respectively. Total and renal clearances in a typical cUTI or HABP/VABP patient were 4.57 and 4.08 liters/h, respectively. Starting dose adjustments for CL(CR) are sufficient for minimizing the variation in plasma exposure across patient populations; adjustments based on other covariates are not warranted. The results support initial dosing on a milligram-per-kilogram basis with adjustments for CL(CR) and BW. Subsequent adjustments based on therapeutic drug management are recommended in certain subsets of patients, including the critically ill and renally impaired. American Society for Microbiology 2019-03-27 /pmc/articles/PMC6496156/ /pubmed/30670433 http://dx.doi.org/10.1128/AAC.02329-18 Text en Copyright © 2019 Trang et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Pharmacology
Trang, Michael
Seroogy, Julie D.
Van Wart, Scott A.
Bhavnani, Sujata M.
Kim, Aryun
Gibbons, Jacqueline A.
Ambrose, Paul G.
Rubino, Christopher M.
Population Pharmacokinetic Analyses for Plazomicin Using Pooled Data from Phase 1, 2, and 3 Clinical Studies
title Population Pharmacokinetic Analyses for Plazomicin Using Pooled Data from Phase 1, 2, and 3 Clinical Studies
title_full Population Pharmacokinetic Analyses for Plazomicin Using Pooled Data from Phase 1, 2, and 3 Clinical Studies
title_fullStr Population Pharmacokinetic Analyses for Plazomicin Using Pooled Data from Phase 1, 2, and 3 Clinical Studies
title_full_unstemmed Population Pharmacokinetic Analyses for Plazomicin Using Pooled Data from Phase 1, 2, and 3 Clinical Studies
title_short Population Pharmacokinetic Analyses for Plazomicin Using Pooled Data from Phase 1, 2, and 3 Clinical Studies
title_sort population pharmacokinetic analyses for plazomicin using pooled data from phase 1, 2, and 3 clinical studies
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6496156/
https://www.ncbi.nlm.nih.gov/pubmed/30670433
http://dx.doi.org/10.1128/AAC.02329-18
work_keys_str_mv AT trangmichael populationpharmacokineticanalysesforplazomicinusingpooleddatafromphase12and3clinicalstudies
AT seroogyjulied populationpharmacokineticanalysesforplazomicinusingpooleddatafromphase12and3clinicalstudies
AT vanwartscotta populationpharmacokineticanalysesforplazomicinusingpooleddatafromphase12and3clinicalstudies
AT bhavnanisujatam populationpharmacokineticanalysesforplazomicinusingpooleddatafromphase12and3clinicalstudies
AT kimaryun populationpharmacokineticanalysesforplazomicinusingpooleddatafromphase12and3clinicalstudies
AT gibbonsjacquelinea populationpharmacokineticanalysesforplazomicinusingpooleddatafromphase12and3clinicalstudies
AT ambrosepaulg populationpharmacokineticanalysesforplazomicinusingpooleddatafromphase12and3clinicalstudies
AT rubinochristopherm populationpharmacokineticanalysesforplazomicinusingpooleddatafromphase12and3clinicalstudies