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Randomised trial of acid inhibition by vonoprazan 10/20 mg once daily vs rabeprazole 10/20 mg twice daily in healthy Japanese volunteers (SAMURAI pH study)

医学 雷贝拉唑 交叉研究 药效学 内科学 胃肠病学 药代动力学 质子抑制剂泵 安慰剂 病理 替代医学
作者
Toshihisa Takeuchi,Takahisa Furuta,Yasuhiro Fujiwara,Mitsushige Sugimoto,Kunio Kasugai,Motoyasu Kusano,Hiroyuki Okada,Takahiro Suzuki,Tomohiro Higuchi,Takuma Kagami,Takahiro Uotani,Mihoko Yamade,Akinari Sawada,Fumio Tanaka,Satoshi Harada,Ota K,Yuichi Kojima,Masaki Murata,Yasuhiro Tamura,Yasushi Funaki
出处
期刊:Alimentary Pharmacology & Therapeutics [Wiley]
卷期号:51 (5): 534-543 被引量:60
标识
DOI:10.1111/apt.15641
摘要

Summary Background Vonoprazan (V), a potassium‐competitive acid blocker, has a more durable acid‐inhibitory effect as compared with standard‐dose proton pump inhibitors (PPIs) but has not been compared with 2‐4 times higher daily PPI doses administered in two divided doses. Aims To evaluate the acid‐inhibitory effect of V 10/20 mg once‐daily (OD; V10/V20) vs rabeprazole (R) 10/20 mg twice‐daily (BID; R20/R40) in healthy Japanese volunteers. Methods This multicentre, randomised, open‐label, two‐period, crossover study compared V10 or V20 vs R20, or V20 vs R40 using three cohorts of 10 healthy Japanese adults. Within each cohort, subjects were randomised to receive V or R for 7 days and, following a washout period ≥7 days, the other treatment for 7 days. On day 6 of each period, 24‐hours multichannel gastric impedance‐pH monitoring was performed. Percent times pH ≥ 3, ≥4 and ≥5 (pH 3, 4 and 5 holding time ratios [HTRs]) in 24 hours were evaluated as primary pharmacodynamic endpoints. Results Acid‐inhibitory effect (24‐hours pH 3 HTR) of V20 was greater than those of R20 (91.0% vs 65.3%; P = .0049) and R40 (98.5% vs 85.9%; P = .0073). Similar results were obtained for 24‐hours pH 4 and 5 HTRs. V20 also achieved greater nocturnal pH 4 (91.5% vs 73.2%; P = .0319) and 5 HTRs (78.8% vs 62.2%; P = .0325) as compared with R40. One subject (20%) developed diarrhoea while receiving R40 which was considered treatment‐related. Conclusions Compared with 2‐4 times the standard daily dose of R, V20 exerts a more potent and durable acid‐inhibitory effect. Trial identifier: UMIN000022198 ( www.umin.ac.jp/ctr/index.htm ).
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