跳至主要内容
临床试验/JPRN-jRCT2031220317
JPRN-jRCT2031220317进行中(未招募)3 期

A double blind, randomized, placebo-controlled trial evaluating the efficacy and safety of BI 1015550 over at least 52 weeks in patients with Idiopathic Pulmonary Fibrosis (IPF)

Saito Isao0 个研究点目标入组 963 人开始时间: 2022年9月3日最近更新:
适应症

试验速览

阶段
3 期
状态
进行中(未招募)
发起方
入组人数
963

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 ot applicable(—)
性别
All

入选标准

  • Patients 40 years old and elder at the time of signed informed consent.
  • -Diagnosis of Idiopathic Pulmonary Fibrosis (IPF)
  • -Forced Vital Capacity (FVC) 45% and grater of predicted normal
  • -Diffusing Capacity for Carbon Monoxide (DLCO) 25% and grater and less than 90% predicted of normall
  • -On stable treatment with nintedanib or pirfenidone for at least 12 weeks or not on treatment with either nintedanib or pirfenidone for at least 8 weeks

排除标准

  • -Relevant airways obstruction (prebronchodilator FEV1/FVC less than 0.7)
  • -Acute IPF exacerbation within 3 months and/or during the screening period
  • -Treated with immunomodulatory medications (other than oral corticosteroids) or prednisone more than15 mg/day or equivalent for respiratory or pulmonary reasons
  • -Active, unstable or uncontrolled vasculitis within 8 weeks
  • -Any suicidal behaviour in the past 2 years
  • -Any suicidal ideation of type 4 or 5 on the C-SSRS in the past 3 months

研究者

发起方
Saito Isao

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