Department of Clinical Pharmacology and Therapeutics, Seoul National University College of Medicine and Hospital, Seoul, Republic of Korea.
Daewoong Pharmaceutical Co., Ltd., Seoul, Republic of Korea.
Aliment Pharmacol Ther. 2020 Dec;52(11-12):1648-1657. doi: 10.1111/apt.16131. Epub 2020 Oct 27.
DWP14012 (fexuprazan), a novel potassium-competitive acid blocker, is under development for the treatment of acid-related disorders.
To compare the pharmacodynamics (PDs), pharmacokinetics (PKs) and safety of DWP14012 among healthy subjects of Korean, Caucasian and Japanese descent.
A randomised, double-blind, placebo-controlled, single- and multiple-dose study was conducted. Ten subjects in each dose group (40, 60 or 80 mg for Koreans; 40 or 80 mg for Caucasians; 20, 40 or 80 mg for Japanese) were randomly assigned to DWP14012 or a placebo. Twenty-four-hour intragastric pH measurements and serial blood samples were collected for PK/PD evaluation. The PK/PD parameters were compared between each ethnicity.
The extent of gastric acid suppression was similar among the ethnicities; the mean percentages of time that the intragastric pH was above 4 after multiple doses of 40 mg in the Korean, Caucasian and Japanese subjects were 64.3%, 62.8% and 70.3%, respectively, and the corresponding values for the 80 mg dose were 94.8%, 90.6% and 90.6% respectively. The changes in serum gastrin were not clinically significant between all three ethnicities. The systemic exposure of DWP14012 was similar between the three ethnicities after the 40 mg doses but slightly lower in Caucasian and Japanese subjects after the 80 mg doses. Gastric acid suppression by DWP14012 showed a clear exposure-response relationship in the three ethnicities.
Gastric acid suppression by DWP14012 was similar among the Korean, Caucasian and Japanese subjects in this study, and the PK, PK-PD relationships and safety were also similar among the three ethnicities. DWP14012 could be used without consideration of ethnicity.
DWP14012(fexuprazan)是一种新型钾竞争性酸阻滞剂,正在开发用于治疗与酸相关的疾病。
比较 DWP14012 在韩国、白种人和日本裔健康受试者中的药效学(PD)、药代动力学(PK)和安全性。
进行了一项随机、双盲、安慰剂对照、单剂量和多剂量研究。每个剂量组(韩国 40、60 或 80mg;白种人 40 或 80mg;日本 20、40 或 80mg)各有 10 名受试者随机分配至 DWP14012 或安慰剂。进行 24 小时胃内 pH 测量和连续采血以进行 PK/PD 评估。比较了每个种族之间的 PK/PD 参数。
不同种族之间的胃酸抑制程度相似;多次给予 40mg 后,韩国、白种人和日本人受试者胃内 pH 值高于 4 的时间百分比分别为 64.3%、62.8%和 70.3%,相应的 80mg 剂量值分别为 94.8%、90.6%和 90.6%。三种族之间血清胃泌素的变化无临床意义。在给予 40mg 后,三种族之间 DWP14012 的全身暴露情况相似,但给予 80mg 后白种人和日本人受试者的暴露量略低。DWP14012 对胃酸的抑制作用在三种族中均表现出明显的暴露-反应关系。
在这项研究中,DWP14012 对韩国、白种人和日本人受试者的胃酸抑制作用相似,三种族之间的 PK、PK-PD 关系和安全性也相似。可以不考虑种族因素使用 DWP14012。