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
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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