跳至主要内容
临床试验/EUCTR2022-001091-34-SI
EUCTR2022-001091-34-SI进行中(未招募)1 期

A double blind, randomized, placebo-controlled trial evaluatingthe efficacy and safety of BI 1015550 over at least 52 weeks inpatients with Idiopathic Pulmonary Fibrosis (IPF) - PDE4 Phase III trial in IPF (Fibroneer- IPF)

Boehringer Ingelheim RCV GmbH & Co KG0 个研究点目标入组 963 人开始时间: 2022年10月6日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
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

性别
All

入选标准

  • Patients =40 years old at the time of signed consent
  • IPF diagnosis based on 2022 ATS/ERS/JRS/ALAT Guidelines
  • FVC =45% of predicted normal
  • DLCO =25% and <90% predicted of normal
  • 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
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 337
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 626

排除标准

  • Relevant airways obstruction (prebronchodilator FEV1/FVC
  • Acute IPF exacerbation within 3 months and/or during the
  • screening period
  • Treated with immunomodulatory medications (other than oral
  • corticosteroids) or prednisone >15 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

相似试验