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首页> 外文期刊>International journal of clinical pharmacology and therapeutics >Effects of food and gender on pharmacokinetics of ticagrelor and its main active metabolite AR-C124910XX in healthy Chinese subjects
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Effects of food and gender on pharmacokinetics of ticagrelor and its main active metabolite AR-C124910XX in healthy Chinese subjects

机译:食品和性别对健康中国科目中TicagreloLoR及其主要活性代谢物AR-C124910xx的影响

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摘要

Objectives: The manuscript was mainly aimed to evaluate effects of food and gender on the pharmacokinetics of ticagrelor and its main active metabolite AR-C124910XX in healthy Chinese subjects observed in the bioequivalence studies of the two formulations of ticagrelor tablets. Materials and methods: The single-dose, two-sequence, two-period and crossover studies were respectively conducted under fasting and fed conditions. Plasma samples were analyzed by an HPLC-MS/MS method. Log-transformed pharmacokinetic parameters of ticagrelor and AR-C124910XX obtained from the trials were compared by the mean of two one-sided t-test. Results: Pharmacokinetic parameters of the two formulations were evaluated. The mean ticagrelor t(max) value was delayed by 0.28 - 0.53 hours owing to meals. A 21.6 - 24.0% (p 0.05) increase in the mean ticagrelor AUC* (body weight-normalized AUC) value was measured (fed vs. fasting). For AR-C124910XX, the mean T1/2 value was delayed by 0.84 - 1.33 hours (p 0.05) due to meals. A 52.0 - 55.8% (p 0.05) decrease in the mean C-max* (body weight-normalized C-max) value and a 15.6 - 16.9% (p 0.05) decrease in the mean AUC* value were observed (fed vs. fasting). The female subjects exhibited higher exposures to ticagrelor and -AR-C124910XX than the male subjects. Compared with other populations, the Chinese subjects in this study experienced a greater decrease in C-max of - AR-C124910XX due to meals. 21 adverse events of mild intensity occurred over the study periods. Conclusion: The studies showed food effects on the absorption of ticagrelor and the formation of AR-C124910XX, and gender effects on exposures to the drug after single oraldose administration.
机译:目的:稿件主要旨在评估食品和性别对Ticagrelences在两种制剂的两种制剂中观察到的健康中国受试者中的TiCagreloLor的药代动力学的影响。材料和方法:单剂量,双序列,两期和交叉研究分别在禁食和喂养条件下进行。通过HPLC-MS / MS法分析等离子体样品。通过两种单侧T检验的平均值比较了从试验中获得的TicagreloR和AR-C124910xx的对数转化的药代动力学参数。结果:评价两种配方的药代动力学参数。由于膳食,平均TiCagrelor T(最大)值延迟0.28 - 0.53小时。测量平均TiCagrelor Auc *(体重标准化AUC)值的21.6-24.0%(p <0.05)增加(FED与禁食)。对于Ar-C124910xx,由于膳食,平均T1 / 2值延迟0.84-1.33小时(P <0.05)。 52.0-55.8%(p <0.05)的平均c-max *(体重归一化C-max)值下降,观察到平均AUC *值的15.6-16.9%(P <0.05)减少(美联储与禁食)。女性受试者对TicagreloLor和-AR-C124910xx显示出更高的暴露,而不是男性受试者。与其他人群相比,本研究中的中国科目经历了由于膳食而导致的C-MAX-AR-C124910xx的更大减少。 21在研究期间发生了温和强度的不良事件。结论:该研究表明,对抗粘胶的吸收和ar-C124910xx的形成,对药物在单次氧化糖给药后对药物的曝光性的性别影响。

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