跳至主要内容
临床试验/JPRN-jRCT2080223842
JPRN-jRCT2080223842已完成2 期

A PHASE 2, OPEN LABEL, SINGLE-ARM STUDY TO ASSESS THE EFFICACY AND SAFETY OF TAS-115 IN PATIENTS WITH IDIOPATHIC PULMONARY FIBROSIS (IPF)

Taiho Pharmaceutical Co., Ltd.0 个研究点目标入组 50 人开始时间: 2018年3月15日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 40age old 至 <= 79age old(—)
性别
All

入选标准

  • 1. Provided written informed consent
  • 2. Confirmed IPF within five years of the registration
  • 3. Have more than 50% of Forced vital capacity
  • 4. Satisfies any of the following
  • Have a history of treatment either with Pirfenidone or Nintedanib
  • Have a history of treatment neither with Pirfenidone nor Nintedanib
  • 5. Able to take medications orally

排除标准

  • 1. Airways obstruction
  • 2. A serious illness or medical condition

研究者

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