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临床试验/EUCTR2013-001746-33-BE
EUCTR2013-001746-33-BE进行中(未招募)1 期

A Multicenter, Randomized, Double-Blind Study to Evaluate Higher Versus Standard Adalimumab Dosing Regimens for Induction and Maintenance Therapy in Subjects with Moderately to Severely Active Crohn's Disease and Evidence of Mucosal Ulceration

AbbVie Deutschland GmbH & Co. KG0 个研究点目标入组 514 人开始时间: 2014年4月3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
514

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

  • 1)Subject is between the ages of 18 to 75 years
  • 2) Diagnosis of colonic, ileocolonic, or ileal Crohn's disease for = 3 months prior to Baseline and confirmed by endoscopy during the Screening period or endoscopy performed within 45 days before Baseline.
  • 3) Crohn's Disease Activity Index (CDAI) = 220 and = 450 at Baseline despite concurrent or prior treatment with a full oral corticosteroids and/or immunosuppressants
  • 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 540
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 60

排除标准

  • 1) Subject with ulcerative colitis or indeterminate colitis
  • 2) Subject who has had surgical bowel resections within the past 6 months or is planning resection
  • 3) Subject with an ostomy or ileoanal pouch
  • 4) Subject with bowel stricture or abdominal or peri-anal abscess
  • 5) Subject who has short bowel syndrome
  • 6) Chronic recurring infections or active TB

研究者

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