Literature DB >> 24670351

Comparative bioavailability of two oral formulations of clopidogrel: determination of clopidogrel and its carboxylic acid metabolite (SR26334) under fasting and fed conditions in healthy subjects.

Nina Brvar, Sylvain Lachance, Ann Lévesque, Marjanca Breznik, Lea Cvitkovič Marčič, Mateja Merslavič, Iztok Grabnar, Tatjana Mateovič-Rojnik.   

Abstract

Two randomized, single dose, 2-period, 2-sequence crossover studies were conducted to evaluate the comparative bioavailability of two clopidogrel formulations under fasting and fed conditions. Assessment of bioequivalence was based upon measurement of plasma concentrations of the parent drug, clopidogrel, and its major (inactive) metabolite, clopidogrel carboxylic acid, using improved methanol-free extraction. Bioequivalence of Krka's formulation to the innovator's formulation was demonstrated under both fasting and fed conditions on 205 volunteers. Confidence intervals for AUC0-t, AUC0-inf and Cmax of clopidogrel and its main metabolite were well within the acceptance range of 80.00 to 125.00 %. Food substantially increased the bioavailability of clopidogrel from both formulations, while no effect of food on the extent and rate of exposure to the metabolite was observed. The effect of food was comparable between the two formulations, as indicated by the same direction and rank of food impact on the bioavailability of both formulations.

Entities:  

Mesh:

Substances:

Year:  2014        PMID: 24670351     DOI: 10.2478/acph-2014-0001

Source DB:  PubMed          Journal:  Acta Pharm        ISSN: 1330-0075            Impact factor:   2.230


  4 in total

1.  Exploring the Relationship of Drug BCS Classification, Food Effect, and Gastric pH-Dependent Drug Interactions.

Authors:  Katie Owens; Sophie Argon; Jingjing Yu; Xinning Yang; Fang Wu; Sue-Chih Lee; Wei-Jhe Sun; Anuradha Ramamoorthy; Lei Zhang; Isabelle Ragueneau-Majlessi
Journal:  AAPS J       Date:  2021-12-27       Impact factor: 4.009

2.  Physiologically Based Pharmacokinetic (PBPK) Modeling of Clopidogrel and Its Four Relevant Metabolites for CYP2B6, CYP2C8, CYP2C19, and CYP3A4 Drug-Drug-Gene Interaction Predictions.

Authors:  Helena Leonie Hanae Loer; Denise Türk; José David Gómez-Mantilla; Dominik Selzer; Thorsten Lehr
Journal:  Pharmaceutics       Date:  2022-04-22       Impact factor: 6.525

3.  Comparative fasting bioavailability of two clopidogrel formulations in healthy Mediterranean volunteers: an in vitro-in vivo correlation.

Authors:  Abdel Naser Zaid; Rowa' Al Ramahi; Rana Bustami; Ayman Mousa; Sewar Khasawneh
Journal:  Drug Des Devel Ther       Date:  2015-04-24       Impact factor: 4.162

4.  Evaluation of potential drug interactions with sodium zirconium cyclosilicate: a single-center, open-label, one sequence crossover study in healthy adults.

Authors:  Mats Någård; William G Kramer; David W Boulton
Journal:  Clin Kidney J       Date:  2020-12-29
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.