Pharmacokinetics and Safety of Triple Therapy with Vonoprazan, Amoxicillin, and Clarithromycin or Metronidazole: A Phase 1, Open-Label, Randomized, Crossover Study

被引:31
|
作者
Sakurai, Yuuichi [1 ]
Shiino, Madoka [1 ,2 ]
Okamoto, Hiroyuki [3 ]
Nishimura, Akira [1 ]
Nakamura, Koki [1 ,4 ]
Hasegawa, Setsuo [5 ,6 ]
机构
[1] Takeda Pharmaceut Co Ltd, Takeda Dev Ctr Japan, Clin Sci, Osaka, Japan
[2] Takeda Pharmaceut Co Ltd, Med Writing Dept, Takeda Dev Ctr Japan, Osaka, Japan
[3] Takeda Pharmaceut Co Ltd, Takeda Dev Ctr Japan, Dept Clin Pharmacol, Osaka, Japan
[4] Takeda Pharmaceut Co Ltd, Japan Pharma Business Unit, CVM Mkt, Tokyo, Japan
[5] Med Corp Houeikai, Sekino Clin Pharmacol Clin, Tokyo, Japan
[6] Pharmaspur Inc, Tokyo, Japan
关键词
Drug interactions; Gastroenterology; Helicobacter pylori; Pharmacokinetics; Potassium-competitive acid blocker; Safety; TAK-438; Triple therapy; Vonoprazan; HELICOBACTER-PYLORI INFECTION; PROTON PUMP INHIBITORS; COMPETITIVE ACID BLOCKER; ERADICATION THERAPY; TAK-438; VONOPRAZAN; GASTRIC-CANCER; CLINICAL-TRIAL; LANSOPRAZOLE; PHARMACODYNAMICS; MANAGEMENT;
D O I
10.1007/s12325-016-0374-x
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Vonoprazan (TAK-438) is a novel potassium-competitive acid blocker that inhibits gastric H+, K+-ATPase. The objectives of this study were to evaluate the influence of triple therapy with vonoprazan-amoxicillin-clarithromycin or vonoprazan-amoxicillin-metronidazole on the pharmacokinetics of each component of the triple therapies (primary) and to evaluate the safety and tolerability of vonoprazan-based triple therapies (secondary) in healthy adults. In this single-center, phase 1, open-label, randomized, four-way crossover study, Helicobacter pylori-negative, healthy Japanese male subjects were randomly assigned to 1 of 4 treatment sequences in two cohorts (12 subjects per cohort). Each treatment sequence comprised four treatment periods separated by a washout period of 7 or 14 days. Pharmacokinetic parameters for vonoprazan, amoxicillin, clarithromycin and metronidazole in single therapy or triple therapies were assessed. All adverse events were recorded. Compared with single therapy, triple therapy with vonoprazan-amoxicillin-clarithromycin increased the area under the plasma concentration-time curve from time 0-12 h (AUC(0-12)) and maximum plasma concentration (C (max)) of plasma vonoprazan free base by 1.846- and 1.868-fold, respectively, and increased the AUC(0-12) and C (max) of plasma clarithromycin by 1.450- and 1.635-fold, respectively. Triple therapy with vonoprazan-amoxicillin-metronidazole had no influence on the pharmacokinetics of vonoprazan or metronidazole. The pharmacokinetics of amoxicillin was not influenced by vonoprazan-based triple therapies. Seven adverse events were reported. Two subjects discontinued because of an adverse event (rash, liver function test abnormal); both events were considered to be study drug-related. In healthy Japanese male subjects, triple therapy with vonoprazan-amoxicillin-clarithromycin increased vonoprazan and clarithromycin exposure. The safety and tolerability profile of triple therapy with vonoprazan-amoxicillin-clarithromycin or vonoprazan-amoxicillin-metronidazole was favorable in this population. Takeda Pharmaceutical Company Ltd. JapicCTI-153102.
引用
收藏
页码:1519 / 1535
页数:17
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