Pharmacokinetics and relative bioavailability of fixed-dose combination of clopidogrel and aspirin versus coadministration of individual formulations in healthy Korean men

被引:5
作者
Choi, Hyang-Ki [1 ]
Ghim, Jong-Lyul [2 ]
Shon, Jihong [1 ,3 ]
Choi, Young-Kyung [1 ]
Jung, Jin Ah [1 ,3 ]
机构
[1] Inje Univ, Dept Pharmacol, Coll Med, Busan, South Korea
[2] Korea Univ, Dept Clin Pharmacol & Toxicol, Coll Med, Anam Hosp, Seoul, South Korea
[3] Inje Univ, Dept Clin Pharmacol, Busan Paik Hosp, 75 Bokji Ro, Busan 47392, South Korea
关键词
comparative pharmacokinetics; fixed-dose combination; clopidogrel/aspirin; bioequivalence; ACETYLSALICYLIC-ACID; PREVENTION; METABOLITE; SAFETY;
D O I
10.2147/DDDT.S109080
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: Simultaneous prescription of clopidogrel and low-dose aspirin is recommended for the treatment of acute coronary syndrome because of improvements in efficacy and patient compliance. In this study, the pharmacokinetics of a fixed-dose combination (FDC) of clopidogrel and aspirin was compared with coadministration of individual formulations to clarify the equivalence of the FDC. Methods: This was a randomized, open-label, two-period, two-treatment, crossover study in healthy Korean men aged 20-55 years. Subjects received two FDC capsules of clopidogrel/aspirin 75/100 mg (test) or two tablets of clopidogrel 75 mg and two capsules of aspirin 100 mg (reference) with a 14-day washout period. Plasma concentrations of clopidogrel, aspirin, and salicylic acid were measured using validated ultraperformance liquid chromatography-tandem mass spectrometry. Bioequivalence was assessed by analysis of variance and calculation of the 90% confidence intervals (CIs) of the ratios of the geometric means (GMRs) for AUC(last) and C-max for clopidogrel and aspirin. Results: Sixty healthy subjects were enrolled, and 53 completed the study. Clopidogrel, aspirin, and salicylic acid showed similar absorption profiles and no significant differences in C-max, AUC(last), and T-max between FDC administration and coadministration of individual formulations. The GMRs (90% CI) for the C-max and AUC(last) of clopidogrel were 1.08 (0.95, 1.23) and 0.93 (0.84, 1.03), respectively. The GMRs (90% CI) for the C-max and AUC(last) of aspirin were 0.98 (0.84, 1.13) and 0.98 (0.93, 1.04), respectively. Both treatments were well tolerated in the study subjects. Conclusion: The FDC of clopidogrel and aspirin was bioequivalent to coadministration of each individual formulation. The FDC capsule exhibited similar safety and tolerability profiles to the individual formulations. Therefore, clopidogrel/aspirin 75 mg/100 mg FDC capsules can be prescribed to improve patient compliance.
引用
收藏
页码:3493 / 3499
页数:7
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