TY - JOUR
T1 - 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)
AU - Takeuchi, Toshihisa
AU - Furuta, Takahisa
AU - Fujiwara, Yasuhiro
AU - Sugimoto, Mitsushige
AU - Kasugai, Kunio
AU - Kusano, Motoyasu
AU - Okada, Hiroyuki
AU - Suzuki, Takahiro
AU - Higuchi, Tomohiro
AU - Kagami, Takuma
AU - Uotani, Takahiro
AU - Yamade, Mihoko
AU - Sawada, Akinari
AU - Tanaka, Fumio
AU - Harada, Satoshi
AU - Ota, Kazuhiro
AU - Kojima, Yuichi
AU - Murata, Masaki
AU - Tamura, Yasuhiro
AU - Funaki, Yasushi
AU - Kawamura, Osamu
AU - Okamoto, Yuki
AU - Fujimoto, Kazuma
AU - Higuchi, Kazuhide
N1 - Funding Information:
This work was funded by EA Pharma Co., Ltd., Tokyo, Japan. We thank EP‐CRUS Co., Ltd., Tokyo, Japan for their technical assistance in data management and statistical analysis. English language editing services were provided by Honnet Co., Ltd., Kyoto, Japan and were funded by EA Pharma Co., Ltd., Tokyo, Japan.
Publisher Copyright:
© 2020 John Wiley & Sons Ltd
PY - 2020/3/1
Y1 - 2020/3/1
N2 - 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).
AB - 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).
KW - crossover
KW - gastric ph monitoring
KW - healthy volunteers
KW - rabeprazole
KW - vonoprazan
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U2 - 10.1111/apt.15641
DO - 10.1111/apt.15641
M3 - Article
C2 - 31990424
AN - SCOPUS:85078656772
SN - 0269-2813
VL - 51
SP - 534
EP - 543
JO - Alimentary Pharmacology and Therapeutics
JF - Alimentary Pharmacology and Therapeutics
IS - 5
ER -