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临床试验/JPRN-jRCT2080221099
JPRN-jRCT2080221099未知1 期

Phase I, Multiple Dose Study of MLN0002 in Patients with Ulcerative Colitis

Takeda Pharmaceutical Company Limited0 个研究点目标入组 12 人开始时间: 2010年5月18日最近更新:
适应症

试验速览

阶段
1 期
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
>= 18age old 至 <= 70age old(—)
性别
All

入选标准

  • 1)Patients with well-defined ulcerative colitis
  • 2)Patients who agree to use routinely adequate contraception
  • 3)Patients weigh at least 40 kg

排除标准

  • 1)Patients for whom surgical intervention for their ulcerative colitis is currently required or anticipated
  • 2)Patients with dysplasia or cancer of colon or rectum
  • 3)Patients with symptoms of intestinal stenosis, history of intestinal resection (except for appendectomy)
  • 4)Patients with intestinal diseases other than ulcerative colitis (radiation colitis, ischemic colitis, drug-induced colitis, Crohn's disease, intestinal Behcet disease, lymphoid follicular hyperplasia, etc.)
  • 5)Patients with presence or history of active or latent tuberculosis
  • 6)Female patients who are pregnant or lactating
  • 7)Patients with prior exposure to MLN0002, natalizumab, rituximab, or efalizumab

研究者

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