埃索美拉唑
法莫替丁
交叉研究
药代动力学
药效学
医学
最大值
内科学
药理学
曲线下面积
胃肠病学
安慰剂
替代医学
病理
作者
Ha Yeon Kim,Jun Gi Hwang,Jae-Won Kim,Chang Hwan Seong,Ji Hyeon Lee,Young‐Sim Choi,Hyo Jin Min,Hyung Son Kim,Hye Yun Kim,Yu Kyong Kim,Min Kyu Park
摘要
OBJECTIVE: RA), is mainly prescribed to alleviate the early symptoms of gastritis. Our aim was to explore the possibilities of low-dose esomeprazole as a treatment of gastritis as well as the pharmacodynamic (PD) properties of esomeprazole and famotidine. MATERIALS AND METHODS: A randomized, multiple-dose, 6-sequence, 3-period crossover study was conducted with a 7-day washout between periods. For each period, the subjects were administered one dose of esomeprazole 10 mg or famotidine 20 mg or esomeprazole 20 mg each day. To evaluate the PDs, the 24-hour gastric pH was recorded after single and multiple doses. The mean percentage of time during which the gastric pH was above 4 was evaluated for PD assessment. To confirm the pharmacokinetic (PK) characteristics of esomeprazole, blood was collected for up to 24 hours after multiple doses. RESULTS: ) for esomeprazole 10 mg compared to 20 mg were 0.3654 (0.3381 - 0.3948) and 0.5066 (0.4601 - 0.5579), respectively. CONCLUSION: The PD parameters of esomeprazole 10 mg were comparable to those of famotidine after multiple doses. These findings provide support for further evaluating the use of 10 mg of esomeprazole as a treatment option for gastritis.
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