替格拉赞与克拉霉素在健康人体内的药动学相互作用评价。

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Minkyung Oh, Heechan Lee, Seokuee Kim, Bongtae Kim, Geun Seog Song, Jae-Gook Shin, Jong-Lyul Ghim
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引用次数: 0

摘要

替戈拉赞是一种新型的钾竞争性酸阻滞剂,用于治疗胃酸相关疾病。克拉霉素作为根除幽门螺杆菌的多种方案之一被广泛应用。本研究比较了替格拉赞和克拉霉素在联合治疗和单药治疗中的药代动力学和安全性,以评估潜在的药物-药物相互作用。在24名健康受试者中进行了一项开放标签、随机、6序列、3期交叉研究。按照指定的顺序,受试者在每期5天内接受指定的治疗。比较替戈拉赞和克拉霉素联合用药与单独用药的PK参数。替格拉赞与克拉霉素合用使替格拉赞的稳态最大血浆浓度(Css,max)和稳态给药间隔血浆浓度-时间曲线下面积(AUCss,tau) (Css,max为1.6倍,AUCss,tau为2.5倍)和M1 (Css,max为2.0倍,AUCss,tau为2.5倍)比单独给药时增加。14-羟基克拉霉素的Css、max和aucs、tau分别增加1.8倍和2.0倍。AUCss。联合给药组克拉霉素的tau值略有升高,但Css、max值不变。24例健康受试者对替戈拉赞与克拉霉素联合用药及单独用药均耐受。当替戈拉赞和克拉霉素合用时,可能存在药物相互作用,导致血浆药物浓度相互增加,但没有引起安全问题。建议有必要深入分析浓度-反应关系,以确定这些浓度变化是否值得临床行动。试验注册:ClinicalTrials.gov标识符:NCT02052336。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Evaluation of pharmacokinetic drug-drug interaction between tegoprazan and clarithromycin in healthy subjects.

Evaluation of pharmacokinetic drug-drug interaction between tegoprazan and clarithromycin in healthy subjects.

Evaluation of pharmacokinetic drug-drug interaction between tegoprazan and clarithromycin in healthy subjects.

Evaluation of pharmacokinetic drug-drug interaction between tegoprazan and clarithromycin in healthy subjects.

Tegoprazan is a novel potassium-competitive acid blocker that treats gastric acid-related diseases. Clarithromycin was widely used as one of various regimens for eradicating Helicobacter pylori. This study compared the pharmacokinetic and safety profile of tegoprazan and clarithromycin between combination therapy and monotherapy to evaluate the potential drug-drug interaction. An open-label, randomized, 6-sequence, 3-period crossover study was conducted in 24 healthy subjects. According to the assigned sequence, the subject was administered the assigned treatment during 5 days in each period. PK parameters of tegoprazan and clarithromycin administered in combination were compared with those of the respective monotherapies. The co-administration of tegoprazan with clarithromycin increased maximum steady-state plasma concentration (Css,max) and area under the plasma concentration-time curve in dosing interval at steady-state (AUCss,tau) of tegoprazan (1.6-fold in Css,max and 2.5-fold in AUCss,tau) and M1 (2.0-fold in Css,max, 2.5-fold in AUCss,tau) than tegoprazan alone. The Css,max and AUCss,tau of 14-hydroxyclarithromycin increased 1.8- and 2.0-fold in co-administration, respectively. The AUCss.tau of clarithromycin was slightly increased in co-administration, but Css,max was not changed. Combination of tegoprazan and clarithromycin and those of the respective monotherapies were tolerated in 24 healthy subjects. There may exist drug interaction that lead to reciprocal increase in plasma drug concentrations when tegoprazan and clarithromycin were administrated in combination and no safety concerns were raised. It is suggested that an in-depth analysis of the concentration-response relationship is necessary to determine whether these concentration changes warrant clinical action.

Trial registration: ClinicalTrials.gov Identifier: NCT02052336.

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来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
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