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临床试验/NL-OMON55460
NL-OMON55460已完成3 期

A Phase 3b Open-label Study to Determine the Long-term Safety and Efficacy of Vedolizumab Subcutaneous in Subjects with Ulcerative Colitis and Crohn*s Disease - Vedolizumab SC Open-Label Extension [MLN0002SC-3030]

Takeda0 个研究点目标入组 12 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
12

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

  • The subject has previously participated in Study MLN0002SC-3027 or
  • MLN0002SC-3031, and, in the opinion of the investigator, tolerated the study
  • drug well. Subjects who withdraw early from Study MLN0002SC-3027 or
  • MLN0002SC-3031 must have withdrawn due to treatment failure (ie, as determined
  • by disease worsening or need for rescue medications from Week 14 of the
  • respective study) during the Maintenance Period.

排除标准

  • * The subject required surgical intervention for UC or CD during or after
  • participation in Study MLN0002SC-3027 or MLN0002SC-3031, currently requires
  • surgical intervention for UC or CD, or is anticipated to require surgical
  • intervention for UC or CD during this study.
  • * The subject has withdrawn from Study MLN0002SC-3027 or MLN0002SC-3031 due to
  • a study drug-related adverse event (AE).

研究者

发起方
Takeda

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