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临床试验/NCT00048295
NCT00048295已完成3 期

ISIS 2302-CS21, Phase 3 Double-Masked, Placebo-Controlled Study of Alicaforsen (ISIS 2302), an Antisense Inhibitor of ICAM-1, for the Treatment of Patients With Active Crohn's Disease

Ionis Pharmaceuticals, Inc.15 个研究点 分布在 6 个国家目标入组 150 人开始时间: 2002年5月1日最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
150
试验地点
15

研究概览

简要总结

ISIS 2302 is an antisense oligonucleotide drug that reduces the production of a specific protein called intercellular adhesion molecule (ICAM-1), a substance that plays a significant role in the increase of inflammation. People with Crohn's disease have been shown to over-produce ICAM-1 in their gut tissues. Alicaforsen works by blocking ICAM-1 messenger RNA, the "instruction" molecule that is required for the production of ICAM-1 protein. This trial will examine effects of alicaforsen delivered by 2-hour intravenous infusion over a four-week period, compared to a placebo. Patients may remain on stable background 5-ASA, antibiotic, or immunosuppressive drugs, and prednisone (or equivalent) at </= 30 mg per day.

研究设计

研究类型
Interventional
分配方式
Randomized
主要目的
Treatment
盲法
Double

入排标准

年龄范围
12 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Age >/= 12 years
  • •Weight >/= 36 kg
  • •CDAI score of 220 - 400
  • •Documentation of Crohn's disease activity by endoscopy, biopsy or imaging in the last 2 years
  • •No TNF-α inhibitor treatment for three months prior to first study drug infusion

排除标准

  • •Known severe, fixed, symptomatic stenosis of the small or large intestine with significant dilation
  • •Extensive external fistulization (> 3 external fistulae which are expressible with gentle compression); colostomy or ileostomy
  • •Active infection, including infectious colitis, or infection with HIV, Hepatitis B or Hepatitis C
  • •Malignancy within 3 years or poorly controlled medical illness
  • •Requires intravenous heparin therapy or with a history of a bleeding problem

研究者

申办方类型
Industry

研究点 (15)

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