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回肠胆汁酸转运体抑制剂依洛比西巴特(5毫克古菲斯片)的药理特性及临床研究结果

[Pharmacological characteristics and clinical study results of ileal bile acid transporter inhibitor elobixibat (GOOFICE tablet 5 mg)].

作者信息

Ikeda Naoki, Taniguchi Shinya, Seki Mitsunori

机构信息

Medical Department, EA Pharma Co., Ltd.

Clinical Development Department, EA Pharma Co., Ltd.

出版信息

Nihon Yakurigaku Zasshi. 2019;153(3):129-138. doi: 10.1254/fpj.153.129.

DOI:10.1254/fpj.153.129
PMID:30867382
Abstract

Elobixibat is a novel small-molecule that acts as an inhibitor of the ileal bile acid transporter (IBAT), and used for chronic constipation in Japan. Elobixibat selectively inhibited IBAT in vitro, and dose-dependently inhibited the absorption of bile acids in vivo. Also, elobixibat dose-dependently increased wet fecal weight in a rat loperamide-induced constipation model. The drug-drug interaction study suggested that elobixibat may have a clinically slight inhibitory effect on P-glycoprotein. In a phase II study with chronic constipation, the recommended dosage for oral administration of elobixibat once daily was estimated to be 10 mg. In a phase 3 study with chronic constipation, the superiority of the elobixibat 10 mg group to the placebo group was demonstrated in the change from baseline (ie, the last week of the 2-week run-in period) in the frequency of spontaneous bowel movements per week during the first week of treatment set as the primary endpoint. In a long-term study in which elobixibat was administered to patients with chronic constipation for 52 weeks, the ameliorating effects of elobixibat on constipation were observed from the first week of treatment and maintained well until week 52. In addition, the safety/tolerability of elobixibat administered once daily for 52 weeks was considered to be acceptable. Therefore, elobixibat has a mechanism of action that differs from any of the existing therapeutic agents for constipation and is expected to become one of the new treatment options for chronic constipation.

摘要

依洛比西巴特是一种新型小分子药物,作为回肠胆汁酸转运体(IBAT)抑制剂,在日本用于治疗慢性便秘。依洛比西巴特在体外选择性抑制IBAT,在体内剂量依赖性抑制胆汁酸吸收。此外,在大鼠洛哌丁胺诱导的便秘模型中,依洛比西巴特剂量依赖性增加湿粪重量。药物相互作用研究表明,依洛比西巴特可能对P-糖蛋白有轻微临床抑制作用。在一项慢性便秘的II期研究中,依洛比西巴特每日口服一次的推荐剂量估计为10毫克。在一项慢性便秘的3期研究中,将治疗第一周每周自发排便频率相对于基线(即2周导入期的最后一周)的变化作为主要终点,结果显示依洛比西巴特10毫克组优于安慰剂组。在一项将依洛比西巴特给予慢性便秘患者52周的长期研究中,从治疗第一周就观察到依洛比西巴特对便秘的改善作用,并一直良好维持到第52周。此外,每日一次服用依洛比西巴特52周的安全性/耐受性被认为是可接受的。因此,依洛比西巴特有别于现有的任何便秘治疗药物的作用机制,有望成为慢性便秘的新治疗选择之一。

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Elobixibat, the first-in-class Ileal Bile Acid Transporter inhibitor, for the treatment of Chronic Idiopathic Constipation.依利洛贝特,一种首创的回肠胆汁酸转运蛋白抑制剂,用于治疗慢性特发性便秘。
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引用本文的文献

1
Uncontrolled, Open-Label Pre-Dinner Administration of Elobixibat in Japanese Adults with Chronic Constipation: A Retrospective Chart Review.在日本慢性便秘成年患者中进行的埃洛比昔巴特不受控、开放标签晚餐前给药:一项回顾性病历审查。
Curr Ther Res Clin Exp. 2020 Nov 16;93:100616. doi: 10.1016/j.curtheres.2020.100616. eCollection 2020.