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临床试验/NCT00143546
NCT00143546No Longer Available不适用

Compassionate Use of Defibrotide for Patients With Veno-Occlusive Disease

St. Jude Children's Research Hospital1 个研究点 分布在 1 个国家开始时间: 2003年11月最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
No Longer Available
试验地点
1

研究概览

简要总结

Veno-occlusive disease (VOD) of the liver is a significant complication for some patients undergoing hematopoietic stem cell transplantation. This disease is thought to be a toxicity secondary to chemotherapy or radiation-induced damage to the epithelial cells of the blood vessels in the liver. VOD is categorized as mild, moderate or severe. Historically, there has been no method to treat the disease. Recently, however, there have been investigations into the use of a new agent called defibrotide.

The primary purpose of this protocol is to provide defibrotide to patients with severe VOD. Because this drug has not been approved by the FDA, use of this medication under the auspices of this IND treatment plan is for compassionate use only.

详细描述

Secondary objectives of this protocol include the following:

  • To describe the toxicities of defibrotide in patients with VOD.
  • To describe the response rate of VOD in patients receiving defibrotide.

研究设计

研究类型
Expanded Access

入排标准

性别
All
接受健康志愿者

入选标准

  • Patients with clinical or pathologic diagnosis of veno-occlusive disease. The following criteria will be used:
  • Hyperbilirubinemia (greater than or equal to 2mg/dl) and two of the following: (hepatomegaly, ascites, or weight gain [greater than or equal to 5% of baseline]); OR,
  • Patient who do not fulfill criteria in #1 but who have pathologic or radiographic evidence of VOD.

排除标准

  • 未提供

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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