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临床试验/EUCTR2015-003472-78-IT
EUCTR2015-003472-78-IT进行中(未招募)1 期

A Randomized, Double-Blind, Placebo-Controlled Phase 4 Study to Evaluate the Efficacy and Safety of Entyvio (Vedolizumab IV) in the Treatment of Chronic Pouchitis - EARNEST

TAKEDA DEVELOPMENT CENTRE EUROPE LTD0 个研究点目标入组 102 人开始时间: 2021年6月14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
102

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.Male or female subjects aged 18 to 80 years, inclusive.
  • 2.¿ History of IPAA for UC completed at least 1 year prior to the Day 1 (Randomization) Visit.
  • 3.¿ Pouchitis that is chronic or recurrent, defined by an mPDAI score> =5 assessed as the average from 3 days immediately prior to the Baseline endoscopy and a minimum endoscopic subscore of 2 (outside the staple or suture line) with either
  • (a) =3 recurrent episodes within 1 year prior to the Screening Period treated with =2 weeks of antibiotic or other prescription therapy,
  • (b) requiring maintenance antibiotic therapy taken continuously for =4 weeks immediately prior to the Baseline Endoscopy Visit.
  • 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 94
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 16

排除标准

  • 1.Crohn’s disease (CD), CD of the pouch, irritable pouch syndrome (IPS), isolated or predominant cuffitis, diverting stoma, or mechanical complications of the pouch.
  • 2.¿ Previous treatment with vedolizumab, natalizumab, efalizumab, rituximab, etrolizumab, or anti-mucosal addressin cell adhesion molecule-1 (MAdCAM-1) therapy.
  • ¿3. Any investigational or approved biologic or biosimilar agent within 60 days of randomization.
  • ¿4. Nonbiologic investigational therapy within 30 days prior to randomization.
  • 5. Active or latent tuberculosis.
  • 6.¿ Chronic hepatitis B virus (HBV) infection or chronic hepatitis C virus (HCV) infection or a known history of human immunodeficiency virus (HIV) infection (or is found to be seropositive at Screening) or subject is immunodeficient.
  • ¿7. Active, severe infection.
  • 8. Positive progressive multifocal leukoencephalopathy (PML) subjective symptom checklist at Screening.

研究者

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