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Pharmacokinetic drug interaction between atorvastatin and ezetimibe in healthy Korean volunteers

Atorvastatin and ezetimibe are frequently co-administered to treat patients with dyslipidemia for the purpose of low-density lipoprotein cholesterol control. However, pharmacokinetic (PK) drug interaction between atorvastatin and ezetimibe has not been evaluated in Korean population. The aim of this...

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Autores principales: Park, Jungsin, Kim, Choon Ok, Jin, Byung Hak, Yang, Seoungwon, Park, Min Soo, Hong, Taegon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Clinical Pharmacology and Therapeutics 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033406/
https://www.ncbi.nlm.nih.gov/pubmed/32095476
http://dx.doi.org/10.12793/tcp.2017.25.4.202
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author Park, Jungsin
Kim, Choon Ok
Jin, Byung Hak
Yang, Seoungwon
Park, Min Soo
Hong, Taegon
author_facet Park, Jungsin
Kim, Choon Ok
Jin, Byung Hak
Yang, Seoungwon
Park, Min Soo
Hong, Taegon
author_sort Park, Jungsin
collection PubMed
description Atorvastatin and ezetimibe are frequently co-administered to treat patients with dyslipidemia for the purpose of low-density lipoprotein cholesterol control. However, pharmacokinetic (PK) drug interaction between atorvastatin and ezetimibe has not been evaluated in Korean population. The aim of this study was to investigate PK drug interaction between two drugs in healthy Korean volunteers. An open-label, randomized, multiple-dose, three-treatment, three-period, Williams design crossover study was conducted in 36 healthy male subjects. During each period, the subjects received one of the following three treatments for seven days: atorvastatin 40 mg, ezetimibe 10 mg, or a combination of both. Blood samples were collected up to 96 h after dosing, and PK parameters of atorvastatin, 2-hydroxyatorvastatin, total ezetimibe (free ezetimibe + ezetimibe-glucuronide), and free ezetimibe were estimated by non-compartmental analysis in 32 subjects who completed the study. Geometric mean ratios (GMRs) with 90% confidence intervals (CIs) of the maximum plasma concentration (C(max,ss)) and the area under the curve within a dosing interval at steady state (AUC(τ,ss)) of atorvastatin when administered with and without ezetimibe were 1.1087 (0.9799–1.2544) and 1.1154 (1.0079–1.2344), respectively. The corresponding values for total ezetimibe were 1.0005 (0.9227–1.0849) and 1.0176 (0.9465–1.0941). There was no clinically significant change in safety assessment related to either atorvastatin or ezetimibe. Co-administration of atorvastatin and ezetimibe showed similar PK and safety profile compared with each drug alone. The PK interaction between two drugs was not clinically significant in healthy Korean volunteers.
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spelling pubmed-70334062020-02-24 Pharmacokinetic drug interaction between atorvastatin and ezetimibe in healthy Korean volunteers Park, Jungsin Kim, Choon Ok Jin, Byung Hak Yang, Seoungwon Park, Min Soo Hong, Taegon Transl Clin Pharmacol Original Article Atorvastatin and ezetimibe are frequently co-administered to treat patients with dyslipidemia for the purpose of low-density lipoprotein cholesterol control. However, pharmacokinetic (PK) drug interaction between atorvastatin and ezetimibe has not been evaluated in Korean population. The aim of this study was to investigate PK drug interaction between two drugs in healthy Korean volunteers. An open-label, randomized, multiple-dose, three-treatment, three-period, Williams design crossover study was conducted in 36 healthy male subjects. During each period, the subjects received one of the following three treatments for seven days: atorvastatin 40 mg, ezetimibe 10 mg, or a combination of both. Blood samples were collected up to 96 h after dosing, and PK parameters of atorvastatin, 2-hydroxyatorvastatin, total ezetimibe (free ezetimibe + ezetimibe-glucuronide), and free ezetimibe were estimated by non-compartmental analysis in 32 subjects who completed the study. Geometric mean ratios (GMRs) with 90% confidence intervals (CIs) of the maximum plasma concentration (C(max,ss)) and the area under the curve within a dosing interval at steady state (AUC(τ,ss)) of atorvastatin when administered with and without ezetimibe were 1.1087 (0.9799–1.2544) and 1.1154 (1.0079–1.2344), respectively. The corresponding values for total ezetimibe were 1.0005 (0.9227–1.0849) and 1.0176 (0.9465–1.0941). There was no clinically significant change in safety assessment related to either atorvastatin or ezetimibe. Co-administration of atorvastatin and ezetimibe showed similar PK and safety profile compared with each drug alone. The PK interaction between two drugs was not clinically significant in healthy Korean volunteers. Korean Society for Clinical Pharmacology and Therapeutics 2017-12 2017-12-20 /pmc/articles/PMC7033406/ /pubmed/32095476 http://dx.doi.org/10.12793/tcp.2017.25.4.202 Text en Copyright © 2017 Translational and Clinical Pharmacology http://creativecommons.org/licenses/by-nc/3.0/ It is identical to the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/).
spellingShingle Original Article
Park, Jungsin
Kim, Choon Ok
Jin, Byung Hak
Yang, Seoungwon
Park, Min Soo
Hong, Taegon
Pharmacokinetic drug interaction between atorvastatin and ezetimibe in healthy Korean volunteers
title Pharmacokinetic drug interaction between atorvastatin and ezetimibe in healthy Korean volunteers
title_full Pharmacokinetic drug interaction between atorvastatin and ezetimibe in healthy Korean volunteers
title_fullStr Pharmacokinetic drug interaction between atorvastatin and ezetimibe in healthy Korean volunteers
title_full_unstemmed Pharmacokinetic drug interaction between atorvastatin and ezetimibe in healthy Korean volunteers
title_short Pharmacokinetic drug interaction between atorvastatin and ezetimibe in healthy Korean volunteers
title_sort pharmacokinetic drug interaction between atorvastatin and ezetimibe in healthy korean volunteers
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033406/
https://www.ncbi.nlm.nih.gov/pubmed/32095476
http://dx.doi.org/10.12793/tcp.2017.25.4.202
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