跳至主要内容
临床试验/EUCTR2020-005770-99-NO
EUCTR2020-005770-99-NO进行中(未招募)1 期

Multi-center, double-blind, randomized, placebo-controlled, phase IIa trial to evaluate spesolimab (BI 655130) efficacy in patients with fibrostenotic Crohn’s Disease

Boehringer Ingelheim Norway KS0 个研究点目标入组 100 人开始时间: 2021年9月23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
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • - Male and female patients, 18 to 75 years when signing informed consent at screening
  • - Established diagnosis of clinical CD prior to screening
  • - Suspicion of symptomatic small bowel stenosis
  • - Presence of abdominal pain after eating or limitation in amount or types of food at screening
  • - 1 or 2 naïve or anastomotic stenoses in the terminal ileum at screening, confirmed by MRE at randomization
  • - Have achieved Symptomatic Stenosis Response before randomization (i.e. 7 day average scores <2 for diary questions on the abdominal pain after eating AND on the limitation in amount or types of food)
  • - Endoscopic activity defined by Colonic Simple Endoscopic Score in CD (SES-CD) =12 after Lead-in Period, at the time of randomization
  • 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 80
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 20

排除标准

  • - No stenosis in reach of ileocolonoscopy
  • - Systemic corticosteroid treatment of current obstructive symptoms for >1 week prior to screening
  • - Endoscopic balloon dilation (EBD) or surgical treatment of the same small bowel stenosis within the last 6 months prior to screening Visit 1
  • - More than 2 smal intestinal stenoses
  • - Patients who require immediate EBD or surgical intervention as per the investigator´s discretion
  • - Failure of >2 different biological drug classes prior to screening (e.g. TNF inhibitors, Integrin Receptor antagonists and
  • IL-12 / IL-23 antagonists)
  • - Current complications of CD at screening Visit 1 and randomization (Day 1) that would possibly confound the evaluation of benefit from treatment with spesolimab
  • - Current stenosis in the colon
  • - Previous strictureplasty on current stricture
  • - Current ileostomy or colostomy
  • - Any kind of bowel resection or diversion within 6 months of screening Visit 1
  • - Any other intra-abdominal surgery (except for abscess drainage) within 3 months prior to screening Visit
  • - Colorectal cancer (CRC) present and past (<5 years) history

研究者

相似试验

进行中(未招募)
1 期
Selatogrel Outcome Study in Suspected Acute Myocardial InfarctioAcute myocardial infarctionMedDRA version: 20.0Level: PTClassification code 10000891Term: Acute myocardial infarctionSystem Organ Class: 10007541 - Cardiac disorders
EUCTR2020-000983-41-BGIdorsia Pharmaceuticals Ltd14,000
进行中(未招募)
1 期
A study to test whether spesolimab helps people with Crohn’s disease who have symptoms of bowel obstructioFibrostenotic Crohn’s DiseaseMedDRA version: 20.0Level: PTClassification code 10011401Term: Crohn's diseaseSystem Organ Class: 10017947 - Gastrointestinal disorders
EUCTR2020-005770-99-DKBoehringer Ingelheim B.V100
进行中(未招募)
1 期
Study to assess the efficacy and safety of ACT-541468 in adult and elderly subjects suffering from difficulties to sleepInsomnia disorderMedDRA version: 20.0Level: PTClassification code 10022437Term: InsomniaSystem Organ Class: 10037175 - Psychiatric disorders
EUCTR2017-004642-20-ESIdorsia Pharmaceuticals Ltd930
招募中
3 期
Multi-center, double-blind, randomized, placebo-controlled, parallel-group study to evaluate the efficacy and safety of self-administered subcutaneous selatogrel for prevention of all-cause death and treatment of acute myocardial infarction in subjects with a recent history of acute myocardial infarctioheart attack10028593acute myocardial infarction
NL-OMON54126Idorsia Pharmaceuticals1,680
进行中(未招募)
1 期
Study to assess the efficacy and safety of ACT-541468 in adult subjects suffering from difficulties to sleepInsomnia disorderMedDRA version: 20.0Level: PTClassification code 10022437Term: InsomniaSystem Organ Class: 10037175 - Psychiatric disorders
EUCTR2016-000826-21-DEActelion Pharmaceuticals Ltd360