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比较pH值研究以评估60毫克双延迟释放右兰索拉唑和40毫克延迟释放埃索美拉唑的单剂量药效学。

Comparator pH study to evaluate the single-dose pharmacodynamics of dual delayed-release dexlansoprazole 60 mg and delayed-release esomeprazole 40 mg.

作者信息

Kukulka Michael, Eisenberg Corey, Nudurupati Sai

机构信息

Clinical Pharmacology.

出版信息

Clin Exp Gastroenterol. 2011;4:213-20. doi: 10.2147/CEG.S24063. Epub 2011 Sep 14.

Abstract

BACKGROUND

This paper describes a Phase 1, single-center, randomized, open-label, two-period crossover study which compared the pharmacodynamic effects of single doses of dexlansoprazole modified-release 60 mg and esomeprazole 40 mg on 24-hour intragastric pH in healthy adult subjects.

METHODS

Forty-four subjects aged 20-54 years were randomized in a 1:1 ratio to two sequence groups defining the order in which they received dexlansoprazole and esomeprazole in periods 1 and 2. Primary pharmacodynamic end points over 24 hours postdose were percentage of time with intragastric pH > 4 and mean pH, and secondary pharmacodynamic end points were percentage of time intragastric pH > 4, and mean pH at 0-12 hours, and at >12-24 hours postdose. Each drug was given after an overnight fast and one hour before breakfast. Continuous pH recording began immediately before dosing through to 24 hours postdose.

RESULTS

At 0-24 hours postdose, the mean percentage of time with pH > 4 for dexlansoprazole and esomeprazole was 58% and 48%, respectively; the difference was statistically significant (P = 0.003). The average of mean pH values at 0-24 hours postdose for dexlansoprazole and esomeprazole were 4.3 and 3.7, respectively; the difference was statistically significant (P < 0.001). At >12-24 hours postdose, mean percentage of time with pH > 4 and average of mean pH were greater for dexlansoprazole (60% and 4.5, respectively) compared with esomeprazole (42% and 3.5, respectively); the difference was statistically significant (P < 0.001 for both intervals). At 0-12 hours postdose, the difference in dexlansoprazole and esomeprazole values for the pharmacodynamic end points was not statistically significant.

CONCLUSION

For the entire 24-hour postdose period, predominantly resulting from the >12-24-hour postdose interval, the average intragastric pH following a single dose of dexlansoprazole 60 mg was higher compared with that observed following a single dose of esomeprazole 40 mg, and the difference was statistically significant.

摘要

背景

本文描述了一项1期、单中心、随机、开放标签、两阶段交叉研究,该研究比较了单剂量60毫克右兰索拉唑缓释剂和40毫克埃索美拉唑对健康成年受试者24小时胃内pH值的药效学作用。

方法

44名年龄在20 - 54岁的受试者按1:1比例随机分为两个序列组,以确定他们在第1阶段和第2阶段接受右兰索拉唑和埃索美拉唑的顺序。给药后24小时内的主要药效学终点是胃内pH值>4的时间百分比和平均pH值,次要药效学终点是给药后0 - 12小时以及>12 - 24小时胃内pH值>4的时间百分比和平均pH值。每种药物在禁食过夜后且早餐前1小时给药。连续pH值记录在给药前立即开始,直至给药后24小时。

结果

给药后0 - 24小时,右兰索拉唑和埃索美拉唑胃内pH值>4的平均时间百分比分别为58%和48%;差异具有统计学意义(P = 0.003)。给药后0 - 24小时右兰索拉唑和埃索美拉唑平均pH值的平均值分别为4.3和3.7;差异具有统计学意义(P < 0.001)。给药后>12 - 24小时,右兰索拉唑胃内pH值>4的平均时间百分比和平均pH值平均值(分别为60%和4.5)高于埃索美拉唑(分别为42%和3.5);差异具有统计学意义(两个时间段P均< 0.001)。给药后0 - 12小时,右兰索拉唑和埃索美拉唑药效学终点值的差异无统计学意义。

结论

在给药后的整个24小时期间,主要是由于给药后>12 - 24小时时间段,单剂量60毫克右兰索拉唑后的平均胃内pH值高于单剂量40毫克埃索美拉唑后的平均胃内pH值,且差异具有统计学意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ca0/3190289/f5b823ef6e4d/ceg-4-213f1.jpg

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