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临床试验/KCT0006590
KCT0006590已完成未知

A randomized, double-blind, placebo-controlled, parallel group, 12 weeks, therapeutic exploratory phase 2 clinical study to evaluate the safety and efficacy of HK-660S in patients with Primary Sclerosing Cholangitis(PSC)

Curome Biosciences0 个研究点目标入组 25 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
入组人数
25

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
17(Year) 至 o Limit(—)
性别
All

入选标准

  • Confirmed diagnosis of Primary Sclerosing Cholangitis(PSC)

排除标准

  • - Clinically significant acute or chronic liver disease of an etiology other than PSC
  • - Secondary or IgG4 related sclerosing cholangitis

研究者

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