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非布司他与非甾体抗炎药联合给药的药代动力学相互作用。

Pharmacokinetic interactions of concomitant administration of febuxostat and NSAIDs.

作者信息

Khosravan Reza, Wu Jing-Tao, Joseph-Ridge Nancy, Vernillet Laurent

机构信息

TAP Pharmaceutical Products, Inc, Lake Forest, Illinois, USA.

出版信息

J Clin Pharmacol. 2006 Aug;46(8):855-66. doi: 10.1177/0091270006289848.

Abstract

To evaluate the effect of febuxostat on the pharmacokinetics of indomethacin and naproxen and vice versa, 2 multiple-dose, 3-period crossover studies were performed in healthy subjects. In study 1, subjects received febuxostat 80 mg once daily, indomethacin 50 mg twice daily, or both. In study 2, subjects received febuxostat 80 mg, naproxen 500 mg twice daily, or both. Twenty-four-hour blood samples were collected on day 5 in study 1 and day 7 in study 2. In study 1, 90% confidence intervals of geometric mean ratios for maximum plasma concentration (Cmax) and area under the curve (AUC) were within the 0.80 to 1.25 no-effect range for febuxostat and indomethacin. In study 2, 90% confidence intervals for febuxostat C(max) and AUC extended above that range, with increases of 28% and 40% in Cmax and AUC24, respectively. However, 90% confidence intervals for naproxen C(max) and AUC were within the 0.80 to 1.25 range. Febuxostat had no effect on the plasma pharmacokinetics of indomethacin and naproxen. Similarly, indomethacin had no effect on the plasma pharmacokinetics of febuxostat. Although naproxen caused an increase in plasma exposure to febuxostat, this increase is not expected to be clinically significant. Therefore, based on the plasma pharmacokinetic data in healthy subjects, febuxostat may be administered with indomethacin or naproxen with no dose adjustments for febuxostat, indomethacin, or naproxen.

摘要

为评估非布司他对吲哚美辛和萘普生药代动力学的影响以及反之亦然的情况,在健康受试者中进行了2项多剂量、3期交叉研究。在研究1中,受试者每日一次接受80 mg非布司他、每日两次接受50 mg吲哚美辛或两者同时服用。在研究2中,受试者接受80 mg非布司他、每日两次接受500 mg萘普生或两者同时服用。在研究1的第5天和研究2的第7天采集24小时血样。在研究1中,非布司他和吲哚美辛的最大血浆浓度(Cmax)和曲线下面积(AUC)的几何平均比值的90%置信区间在0.80至1.25的无效应范围内。在研究2中,非布司他C(max)和AUC的90%置信区间超出了该范围,Cmax和AUC24分别增加了28%和40%。然而,萘普生C(max)和AUC的90%置信区间在0.80至1.25范围内。非布司他对吲哚美辛和萘普生的血浆药代动力学无影响。同样,吲哚美辛对非布司他的血浆药代动力学也无影响。虽然萘普生导致非布司他的血浆暴露增加,但预计这种增加在临床上无显著意义。因此,根据健康受试者的血浆药代动力学数据,非布司他可与吲哚美辛或萘普生联合使用,无需对非布司他、吲哚美辛或萘普生进行剂量调整。

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