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临床试验/NCT00258180
NCT00258180已完成2 期

High-Dose Cyclophosphamide for the Treatment of Severe Autoimmune Enteropathy

Johns Hopkins University1 个研究点 分布在 1 个国家目标入组 3 人开始时间: 2005年8月15日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
3
试验地点
1
主要终点
Number of Participants With Treatment-free Remission at 1 Year After Study Completion

研究概览

简要总结

RATIONALE: Cyclophosphamide may help control the symptoms of autoimmune enteropathy .

PURPOSE: This phase II trial is studying how well cyclophosphamide works in treating young patients with severe autoimmune enteropathy.

详细描述

OBJECTIVES:

Primary

  • Determine the rate of treatment-free remission in young patients with severe autoimmune enteropathy treated with high-dose cyclophosphamide.

Secondary

  • Determine the toxic effects of this drug in these patients.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
1 Year 至 21 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

severe autoimmune enteropathy

Experimental

Young patients with severe autoimmune enteropathy receive cyclophosphamide IV over 1 hour on days 1-4. Patients then receive filgrastim (G-CSF) IV or subcutaneously once daily beginning on day 10 and continuing for 3 days or until blood counts recover

干预措施: filgrastim (Biological)

severe autoimmune enteropathy

Experimental

Young patients with severe autoimmune enteropathy receive cyclophosphamide IV over 1 hour on days 1-4. Patients then receive filgrastim (G-CSF) IV or subcutaneously once daily beginning on day 10 and continuing for 3 days or until blood counts recover

干预措施: cyclophosphamide (Drug)

结局指标

主要结局

Number of Participants With Treatment-free Remission at 1 Year After Study Completion

时间窗: 1 year

Number of participants off therapy 1 year after study completion without relapse.

Number of Participants Experiencing Intervention-related Adverse Events, as Defined by CTCAE at 1 Month

时间窗: 1 month

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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