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Pharmacokinetic equivalence study of nonsteroidal anti-inflammatory drug etoricoxib
PURPOSE: The current study aimed to evaluate whether a generic product of etoricoxib 120 mg film-coated tablet (the test drug) was bioequivalent to the reference product (Arcoxia® film-coated tablet 120 mg). METHODS: This was a randomized, open-label, two-sequence, crossover study under fasting cond...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5896653/ https://www.ncbi.nlm.nih.gov/pubmed/29670410 http://dx.doi.org/10.2147/CPAA.S161024 |
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author | Tjandrawinata, Raymond R Setiawati, Arini Nofiarny, Dwi Susanto, Liana W Setiawati, Effi |
author_facet | Tjandrawinata, Raymond R Setiawati, Arini Nofiarny, Dwi Susanto, Liana W Setiawati, Effi |
author_sort | Tjandrawinata, Raymond R |
collection | PubMed |
description | PURPOSE: The current study aimed to evaluate whether a generic product of etoricoxib 120 mg film-coated tablet (the test drug) was bioequivalent to the reference product (Arcoxia® film-coated tablet 120 mg). METHODS: This was a randomized, open-label, two-sequence, crossover study under fasting condition, with a 14-day washout period, involving 26 healthy adult male and female subjects. Blood samples were taken and analyzed for plasma concentrations of etoricoxib (Chemical Abstracts Service [CAS] 202409-33-4) using a high-pressure liquid chromatography–ultraviolet detector (HPLC-UV) system capable of measuring etoricoxib concentrations ranging from 5.00 to 5002.90 ng/mL, with the lowest limit of quantitation of 5.00 ng/mL. A noncompartmental method was used to determine the pharmacokinetic parameters of a single-dose administration of the drug, including the area under plasma concentration–time curve from time zero to the time of last observed concentration (AUC(0−)(t)), the area under plasma concentration–time curve from time zero to infinity (AUC(0−∞)), the maximum plasma concentration (C(max)), the time to reach the maximum plasma concentration (t(max)), and the terminal half-life (t(½)). RESULTS: After a single-dose administration of etoricoxib 120 mg film-coated tablet, the mean (SD) values for the AUC(0–72h) and C(max) of the test drug were 45913.42 (13142.19) ng·h/mL and 3155.93 (752.81) ng/mL, respectively; the values for the reference drug were 44577.20 (13541.85) ng·h/mL and 2915.13 (772.81) ng/mL, respectively. The geometric mean ratios (90% CIs) of the test drug/reference drug were 103.40% (98.70%–108.32%) for AUC(0–72h) and 109.26% (100.18%–119.18%) for C(max). No clinically significant differences in t(max) and t(½)values were found between the test drug and the reference drug. No adverse events were experienced by the subjects during this study. CONCLUSION: The present study demonstrated that the evaluated generic etoricoxib 120 mg film-coated tablets were bioequivalent to the reference drug. |
format | Online Article Text |
id | pubmed-5896653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-58966532018-04-18 Pharmacokinetic equivalence study of nonsteroidal anti-inflammatory drug etoricoxib Tjandrawinata, Raymond R Setiawati, Arini Nofiarny, Dwi Susanto, Liana W Setiawati, Effi Clin Pharmacol Original Research PURPOSE: The current study aimed to evaluate whether a generic product of etoricoxib 120 mg film-coated tablet (the test drug) was bioequivalent to the reference product (Arcoxia® film-coated tablet 120 mg). METHODS: This was a randomized, open-label, two-sequence, crossover study under fasting condition, with a 14-day washout period, involving 26 healthy adult male and female subjects. Blood samples were taken and analyzed for plasma concentrations of etoricoxib (Chemical Abstracts Service [CAS] 202409-33-4) using a high-pressure liquid chromatography–ultraviolet detector (HPLC-UV) system capable of measuring etoricoxib concentrations ranging from 5.00 to 5002.90 ng/mL, with the lowest limit of quantitation of 5.00 ng/mL. A noncompartmental method was used to determine the pharmacokinetic parameters of a single-dose administration of the drug, including the area under plasma concentration–time curve from time zero to the time of last observed concentration (AUC(0−)(t)), the area under plasma concentration–time curve from time zero to infinity (AUC(0−∞)), the maximum plasma concentration (C(max)), the time to reach the maximum plasma concentration (t(max)), and the terminal half-life (t(½)). RESULTS: After a single-dose administration of etoricoxib 120 mg film-coated tablet, the mean (SD) values for the AUC(0–72h) and C(max) of the test drug were 45913.42 (13142.19) ng·h/mL and 3155.93 (752.81) ng/mL, respectively; the values for the reference drug were 44577.20 (13541.85) ng·h/mL and 2915.13 (772.81) ng/mL, respectively. The geometric mean ratios (90% CIs) of the test drug/reference drug were 103.40% (98.70%–108.32%) for AUC(0–72h) and 109.26% (100.18%–119.18%) for C(max). No clinically significant differences in t(max) and t(½)values were found between the test drug and the reference drug. No adverse events were experienced by the subjects during this study. CONCLUSION: The present study demonstrated that the evaluated generic etoricoxib 120 mg film-coated tablets were bioequivalent to the reference drug. Dove Medical Press 2018-04-06 /pmc/articles/PMC5896653/ /pubmed/29670410 http://dx.doi.org/10.2147/CPAA.S161024 Text en © 2018 Tjandrawinata et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Tjandrawinata, Raymond R Setiawati, Arini Nofiarny, Dwi Susanto, Liana W Setiawati, Effi Pharmacokinetic equivalence study of nonsteroidal anti-inflammatory drug etoricoxib |
title | Pharmacokinetic equivalence study of nonsteroidal anti-inflammatory drug etoricoxib |
title_full | Pharmacokinetic equivalence study of nonsteroidal anti-inflammatory drug etoricoxib |
title_fullStr | Pharmacokinetic equivalence study of nonsteroidal anti-inflammatory drug etoricoxib |
title_full_unstemmed | Pharmacokinetic equivalence study of nonsteroidal anti-inflammatory drug etoricoxib |
title_short | Pharmacokinetic equivalence study of nonsteroidal anti-inflammatory drug etoricoxib |
title_sort | pharmacokinetic equivalence study of nonsteroidal anti-inflammatory drug etoricoxib |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5896653/ https://www.ncbi.nlm.nih.gov/pubmed/29670410 http://dx.doi.org/10.2147/CPAA.S161024 |
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