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临床试验/EUCTR2019-003334-16-BG
EUCTR2019-003334-16-BG进行中(未招募)1 期

Randomised, double-blind, placebo-controlled, multicentre study to compare the efficacy and safety of novel 4 mg budesonide suppository in combination with oral mesalazine versus oral mesalazine monotherapy in patients with acute ulcerative colitis

Dr. Falk Pharma GmbH0 个研究点目标入组 360 人开始时间: 2020年12月2日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
360

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

  • Signed informed consent,
  • Man or woman between 18 and 75 years of age,
  • Acute ulcerative colitis,
  • New diagnosis or established disease,
  • diagnosis confirmed by total colonoscopy and biopsy
  • Mildly to moderately active ulcerative colitis (3 < modified UC-DAI < 11), with rectal bleeding subscore of = 1, and endoscopic subscore of = 2 at the most active site in the segment of the rectum
  • 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 282
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 78

排除标准

  • Crohn’s disease, indeterminate colitis, ischemic colitis, diverticular disease-associated colitis, microscopic colitis
  • Presence of colitis of a different origin (e.g. infectious or parasitic, drug-induced),
  • Previous colonic surgery (except appendectomy, haemorrhoidectomy, and endoscopic removal of polyps),
  • Abnormal laboratory values, presence of or suspected concomitant disease(s) that could affect study-specific assessments and/or their evaluation, or might compromise patients' safety and/or compliance (e.g. organic diseases or infections of the gastrointestinal tract (with exceptions), certain malignancies or cancers, certain metabolic disorders)
  • Regular oral treatment with more than 2.4 g/d mesalazine (or therapeutic equivalent, i.e., either > 2.4 g/d olsalazine, > 5.6 g/d balsalazide, or > 6.2 g/d sulfasalazine) within the last 4 weeks prior to baseline,
  • Regular rectal treatment with more than 0.5 g/d mesalazine, olsalazine or more than 1 g/d sulfasalazine within the last 4 weeks prior to baseline,
  • Oral/rectal/intravenous corticosteroids therapy within the last 4 weeks priorto screening endoscopy,
  • For Germany only: diagnosis of active COVID-19

研究者

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