YH4808在健康受试者中的药代动力学和药效学比较,以确定合适的给药方案。
Comparison of the pharmacokinetics and pharmacodynamics of YH4808 in healthy subjects for defining an appropriate dosing regimen.
作者信息
Yoon Sukyong, Oh EunSil, Park Min Soo, Jang Seong Bok, Byun Hae Mi, Park Hyeonsoo, Kim Heeyoung, Kim Choon Ok
机构信息
Department of Clinical Pharmacology, Severance Hospital, Yonsei University College of Medicine, Seoul 03722, Korea.
Department of Pharmacology, Yonsei University College of Medicine, Seoul 03722, Korea.
出版信息
Transl Clin Pharmacol. 2021 Sep;29(3):150-159. doi: 10.12793/tcp.2021.29.e15. Epub 2021 Sep 17.
UNLABELLED
YH4808 is a novel potassium-competitive acid blocker developed for gastric acid-related disorders. Previous studies indicate its potential to improve symptoms of gastric acid-related disorders. The current study was aimed to find the optimal regimen of YH4808 for night time pH control. This study was performed in two parts. Each was a randomized, open-label, active-controlled, multiple-doses, two-treatment, two-period crossover study conducted in 20 healthy Korean volunteers. Subjects were randomly assigned to one of the four groups. The three groups received different dosage regimens of YH4808 (100 mg twice a day, 200 mg once a day, or 200 mg twice a day), and the fourth group received esomeprazole 40 mg twice a day. The pharmacokinetic parameters demonstrated that the systemic exposure of YH4808 increased in a dose-proportional manner. The difference in the proportion of time above pH 4 over 24 h from the baseline was the greatest in the group receiving YH4808 200 mg twice a day. The values of the area under the effect curve at night time (12 A.M.-7 A.M.) were higher in all YH4808 groups than in the esomeprazole group. However, the differences among the YH4808 groups were not statistically significant (p > 0.05). YH4808 exhibited potential for better pH control during the night in comparison to esomeprazole. The optimal regimen for night time pH control among all the YH4808 regimens was 200 mg twice a day.
TRIAL REGISTRATION
ClinicalTrials.gov Identifier: NCT01761513.
未标注
YH4808是一种为治疗胃酸相关疾病而研发的新型钾离子竞争性酸阻滞剂。先前的研究表明其具有改善胃酸相关疾病症状的潜力。本研究旨在探寻YH4808控制夜间pH值的最佳给药方案。本研究分为两个部分。每部分均为在20名健康韩国志愿者中进行的随机、开放标签、活性对照、多剂量、双治疗、双周期交叉研究。受试者被随机分配至四组中的一组。三组接受不同剂量方案的YH4808(每日两次,每次100毫克;或每日一次,每次200毫克;或每日两次,每次200毫克),第四组接受每日两次,每次40毫克的埃索美拉唑。药代动力学参数表明,YH4808的全身暴露呈剂量比例增加。在每日两次服用200毫克YH4808的组中,24小时内pH值高于4的时间比例与基线相比差异最大。所有YH4808组夜间(上午12点至上午7点)效应曲线下面积的值均高于埃索美拉唑组。然而,YH4808组之间的差异无统计学意义(p>0.05)。与埃索美拉唑相比,YH4808在夜间显示出更好的pH值控制潜力。在所有YH4808给药方案中,夜间pH值控制的最佳方案是每日两次,每次200毫克。
试验注册
ClinicalTrials.gov标识符:NCT01761513。
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