跳至主要内容
临床试验/NL-OMON40152
NL-OMON40152撤回3 期

engthening Adalimumab Dosing Interval in IBD patients in long term remission, the LADI study. - LADI study

Erasmus MC, Universitair Medisch Centrum Rotterdam0 个研究点目标入组 72 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
撤回
入组人数
72

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
18 至 99(—)

入选标准

  • Age 18 or older
  • Written informed consent.
  • Previous diagnosis of ileocolonic Crohn*s disease or ulcerative colitis
  • In sustained clinical remission for at least 6 months whilst being treated with adalimumab
  • Adalimumab dosed at 40mg, once every 2 weeks
  • Full clinical response and disease control, defined as
  • -Absence of intestinal or extra-intestinal symptoms, as judged by both patient and physician
  • -Fecal calprotectin < 200 µg/g and CRP within normal range
  • -Full endoscopic remission (no ulcera) assessed at least within 12 months before inclusion
  • Permitted concomitant therapy: aminosalicylates, azathioprine, 6-mercatopurine and methotrexate at stable dose for 12 weeks

排除标准

  • Imminent need for IBD-related surgery
  • Actively draining perianal fistula
  • Pregnancy or lactation
  • Other significant medical illness that might interfere with this study (such as current malignancy, immunodeficiency syndromes and psychiatric illness)

研究者

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