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Population Pharmacokinetic Analysis for Imipenem–Relebactam in Healthy Volunteers and Patients With Bacterial Infections

Relebactam is a small‐molecule β‐lactamase inhibitor developed as a fixed‐dose combination with imipenem/cilastatin. The pharmacokinetics of relebactam and imipenem across 10 clinical studies were analyzed using data from adult healthy volunteers and patients with bacterial infections. Renal functio...

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Detalles Bibliográficos
Autores principales: Bhagunde, Pratik, Patel, Parul, Lala, Mallika, Watson, Kenny, Copalu, William, Xu, Ming, Kulkarni, Pooja, Young, Katherine, Rizk, Matthew L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6813166/
https://www.ncbi.nlm.nih.gov/pubmed/31508899
http://dx.doi.org/10.1002/psp4.12462
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author Bhagunde, Pratik
Patel, Parul
Lala, Mallika
Watson, Kenny
Copalu, William
Xu, Ming
Kulkarni, Pooja
Young, Katherine
Rizk, Matthew L.
author_facet Bhagunde, Pratik
Patel, Parul
Lala, Mallika
Watson, Kenny
Copalu, William
Xu, Ming
Kulkarni, Pooja
Young, Katherine
Rizk, Matthew L.
author_sort Bhagunde, Pratik
collection PubMed
description Relebactam is a small‐molecule β‐lactamase inhibitor developed as a fixed‐dose combination with imipenem/cilastatin. The pharmacokinetics of relebactam and imipenem across 10 clinical studies were analyzed using data from adult healthy volunteers and patients with bacterial infections. Renal function estimated by creatinine clearance significantly affected the clearance of both compounds, whereas weight and health status were of less clinical significance. Simulations were used to calculate probability of joint target attainment (ratio of free drug area under the curve from 0 to 24 hours to minimum inhibitory concentration (MIC) for relebactam and percentage of time the free drug concentration exceeded the MIC for imipenem) for the proposed imipenem/relebactam dose of 500/250 mg, with adjustments for patients with renal impairment, administered as a 30‐minute intravenous infusion four times daily. These dosing regimens provide sufficient antibacterial coverage (MIC ≤ 4 μg/mL) for all renal groups.
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spelling pubmed-68131662019-10-30 Population Pharmacokinetic Analysis for Imipenem–Relebactam in Healthy Volunteers and Patients With Bacterial Infections Bhagunde, Pratik Patel, Parul Lala, Mallika Watson, Kenny Copalu, William Xu, Ming Kulkarni, Pooja Young, Katherine Rizk, Matthew L. CPT Pharmacometrics Syst Pharmacol Research Relebactam is a small‐molecule β‐lactamase inhibitor developed as a fixed‐dose combination with imipenem/cilastatin. The pharmacokinetics of relebactam and imipenem across 10 clinical studies were analyzed using data from adult healthy volunteers and patients with bacterial infections. Renal function estimated by creatinine clearance significantly affected the clearance of both compounds, whereas weight and health status were of less clinical significance. Simulations were used to calculate probability of joint target attainment (ratio of free drug area under the curve from 0 to 24 hours to minimum inhibitory concentration (MIC) for relebactam and percentage of time the free drug concentration exceeded the MIC for imipenem) for the proposed imipenem/relebactam dose of 500/250 mg, with adjustments for patients with renal impairment, administered as a 30‐minute intravenous infusion four times daily. These dosing regimens provide sufficient antibacterial coverage (MIC ≤ 4 μg/mL) for all renal groups. John Wiley and Sons Inc. 2019-10-04 2019-10 /pmc/articles/PMC6813166/ /pubmed/31508899 http://dx.doi.org/10.1002/psp4.12462 Text en © 2019 Merck Sharp & Dohme Corp. a subsidiary of Merck & Co. Inc. CPT: Pharmacometrics & Systems Pharmacology published by Wiley Periodicals, Inc. on behalf of the American Society for Clinical Pharmacology and Therapeutics. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research
Bhagunde, Pratik
Patel, Parul
Lala, Mallika
Watson, Kenny
Copalu, William
Xu, Ming
Kulkarni, Pooja
Young, Katherine
Rizk, Matthew L.
Population Pharmacokinetic Analysis for Imipenem–Relebactam in Healthy Volunteers and Patients With Bacterial Infections
title Population Pharmacokinetic Analysis for Imipenem–Relebactam in Healthy Volunteers and Patients With Bacterial Infections
title_full Population Pharmacokinetic Analysis for Imipenem–Relebactam in Healthy Volunteers and Patients With Bacterial Infections
title_fullStr Population Pharmacokinetic Analysis for Imipenem–Relebactam in Healthy Volunteers and Patients With Bacterial Infections
title_full_unstemmed Population Pharmacokinetic Analysis for Imipenem–Relebactam in Healthy Volunteers and Patients With Bacterial Infections
title_short Population Pharmacokinetic Analysis for Imipenem–Relebactam in Healthy Volunteers and Patients With Bacterial Infections
title_sort population pharmacokinetic analysis for imipenem–relebactam in healthy volunteers and patients with bacterial infections
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6813166/
https://www.ncbi.nlm.nih.gov/pubmed/31508899
http://dx.doi.org/10.1002/psp4.12462
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