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临床试验/2024-517502-28-01
2024-517502-28-01招募中4 期

Subcutaneous vedolizumab drug de-escalation using therapeutic drug monitoring in inflammatory bowel disease: a randomized controlled pilot study

Amsterdam UMC Stichting1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年1月14日最近更新:

试验速览

阶段
4 期
状态
招募中
入组人数
40
试验地点
1
主要终点
cost-effectiveness of therapeutic drug monitoring based drug de-escalation

研究概览

简要总结

To evaluate whether subcutaneous vedolizumab therapeutic drug monitoring (TDM)-guided de-escalation will be cost-effective, compared to normal dosing regimen in patients with inflammatory bowel disease in remission.

入排标准

年龄范围
18 years 至 65+ years(65+ Years, 18-64 Years)
接受健康志愿者

入选标准

  • crohn's disease or ulcerative colitis in remission

排除标准

  • presence of anti-drug antibodies against vedolizumab
  • Patients with short bowel syndrome, an ostomy or a symptomatic stricture

结局指标

主要结局

cost-effectiveness of therapeutic drug monitoring based drug de-escalation

cost-effectiveness of therapeutic drug monitoring based drug de-escalation

次要结局

未报告次要终点

研究者

申办方类型
Hospital/Clinic/Other health care facility
责任方
Principal Investigator
主要研究者

S.I. Anjie

Scientific

Amsterdam UMC Stichting

研究点 (1)

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