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呋喹替尼在健康受试者中的食物效应及pH依赖性药物相互作用评估。

Assessment of Food Effect and pH-Dependent Drug-Drug Interactions of Fruquintinib in Healthy Subjects.

作者信息

Gonzalez Martha, Yang Zhao, Schelman William R, Zhou Xiaofei, Gupta Neeraj, Chien Caly

机构信息

HUTCHMED International Corporation, Florham Park, New Jersey, USA.

Takeda Development Center Americas, Inc. (TDCA), Lexington, Massachusetts, USA.

出版信息

Clin Transl Sci. 2025 Mar;18(3):e70168. doi: 10.1111/cts.70168.

Abstract

This two-sequence, three-period study (NCT04645940) was designed to evaluate the effect of food and concomitant rabeprazole, a proton pump inhibitor, on the pharmacokinetics (PK) and safety of fruquintinib and its metabolite M11 after a single oral dose of fruquintinib 5 mg in healthy subjects. In the food effect treatment periods, 14 subjects were randomized in a 1:1 ratio utilizing a two-sequence (fed/fasted vs. fasted/fed), two-period, cross-over design. Fruquintinib was administered on Day 1 (Period 1) and Day 15 (Period 2). In the drug-interaction period (Period 3), all subjects received rabeprazole 40 mg 1 h prior to fruquintinib under fasted conditions, following a 6-day lead-in of rabeprazole 40 mg once daily. PK samples to measure fruquintinib and M11 were collected pre-dose and over 168 h after fruquintinib dosing. Administration of fruquintinib with a high-fat meal resulted in similar systemic exposure compared with fasted conditions. In addition, coadministration of fruquintinib with rabeprazole resulted in similar exposure compared with fruquintinib alone. For both evaluations, 90% confidence intervals for the ratio of geometric least square mean of the area under the curve and peak concentration for fruquintinib and M11 were entirely within 80%-125% bounds. The study results showed no effects of food or rabeprazole on fruquintinib PK, and support that fruquintinib can be taken without regard to food or concurrent gastric acid-reducing agents.

摘要

这项两序列、三阶段研究(NCT04645940)旨在评估食物以及质子泵抑制剂雷贝拉唑对健康受试者单次口服5毫克呋喹替尼后其药代动力学(PK)及代谢物M11的安全性的影响。在食物效应治疗阶段,14名受试者采用两序列(进食/禁食与禁食/进食)、两阶段交叉设计,按1:1比例随机分组。呋喹替尼于第1天(第1阶段)和第15天(第2阶段)给药。在药物相互作用阶段(第3阶段),在禁食条件下,所有受试者在每日一次服用40毫克雷贝拉唑导入6天后,于服用呋喹替尼前1小时服用40毫克雷贝拉唑。在给药前及呋喹替尼给药后168小时内采集用于测量呋喹替尼和M11的PK样本。与禁食条件相比,高脂餐伴服呋喹替尼导致的全身暴露相似。此外,与单独服用呋喹替尼相比,呋喹替尼与雷贝拉唑合用时的暴露相似。对于这两项评估,呋喹替尼和M11曲线下面积及峰浓度的几何最小二乘均值之比的90%置信区间完全在80%-125%范围内。研究结果表明食物或雷贝拉唑对呋喹替尼的PK无影响,并支持呋喹替尼服用时无需考虑食物或同时服用的胃酸还原剂。

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