跳至主要内容
临床试验/jRCT2031240681
jRCT2031240681进行中(未招募)不适用

An open-label pharmacokinetic study of TS-172 in patients on hemodialysis

Taisho Pharmaceutical Co., LTD.0 个研究点目标入组 6 人开始时间: 2025年3月22日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
6

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Single Arm Study
干预模型
Single Assignment
主要目的
Treatment Purpose
盲法
Open(masking Not Used)

入排标准

年龄范围
18age old over 至 75age old not(—)
性别
Male

入选标准

  • (1) Japanese male patients (outpatients) with chronic kidney disease receiving hemodialysis (HD or HDF) 3 times a week for at least 12 weeks prior to the screening test
  • (2) Patients aged >= 18 and < 75 years at the time of obtaining informed consent

排除标准

  • (1) Patients with gastric or intestinal ulceration or a history of them within the past year prior to the date of initiation of treatment, or patients with inflammatory bowel disease or irritable bowel syndrome, or a history of these within the past 5 years prior to the date of initiation of treatment
  • (2) Patients scheduled for renal transplantation, home hemodialysis or change of dialysis facility (transfer or temporary dialysis at other hospital) during the study period
  • (3) Patients who frequently experience diarrhea (defined as Bristol Stool Scale score of 6 or higher)

研究者

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