NL-OMON45760已完成4 期
A Randomized DoubleBlind Phase 4 Study to Evaluate the Safety and Proportion of Subjects With Fistula Healing in 2 Dose Regimens of Entyvio (Vedolizumab IV) in the Treatment of Fistulizing Crohn*s Disease (ENTERPRISE) - Vedolizumab IV 300 mg in the Treatment of Fistulizing Crohn's Disease
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 20
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
- •Adult subjects, aged 18 to 80 years, inclusive, with moderately to severely active CD and 1 to 3 draining perianal fistula(e) of at least 2 weeks duration.
- •Subjects who have historically had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a TNF-a antagonist for their underlying CD (does not require treatment failure for currently active draining fistula); for subjects from France only: subjects who have historically failed (ie, had an inadequate response with, lost response to, or was intolerant to) infliximab for treatment of their underlying CD or fistulizing CD.
排除标准
- •Subjects who have perianal abscesses greater than 2 cm or an abscess that the investigator feels requires drainage based on either clinical assessment or MRI.
- •Subjects who have a CDAI score greater than 400.
- •Subjects who have ileostomy, colostomy, or known fixed symptomatic stenosis of the intestine.
- •Subjects who have significant anal or rectal stenosis.
- •Subjects who have any evidence of an active infection (eg, sepsis, cytomegalovirus, or listeriosis) during screening, other than related to the fistula(e).
- •Subjects who have a positive progressive multifocal leukoencephalopathy (PML) subjective checklist.
- •Subjects who have received any investigational or approved biologic or biosimilar agent within 60 days of randomization.
- •Subjects who have had prior exposure to vedolizumab, natalizumab, efalizumab, rituximab, etrolizumab, or antimucosal addressin cell adhesion molecule-1 (MAdCAM-1) therapy.
- •Subjects who have active or latent tuberculosis.
- •Subjects who have a known history of hepatitis B virus (HBV), hepatitis C virus (HCV), acquired human immunodeficiency virus (HIV), or are found to be seropositive at Screening.
研究者
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