跳至主要内容
临床试验/NCT00006013
NCT00006013已完成2 期

Phase II Trial of SU5416 as Treatment for Refractory/Relapsed Multiple Myeloma

Fox Chase Cancer Center8 个研究点 分布在 1 个国家目标入组 21 人开始时间: 2000年6月最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
21
试验地点
8

研究概览

简要总结

RATIONALE: SU5416 may stop the growth of multiple myeloma by stopping blood flow to the cancer cells.

PURPOSE: Phase II trial to study the effectiveness of SU5416 in treating patients who have refractory or relapsed multiple myeloma.

详细描述

OBJECTIVES: I. Determine the response rate and response duration of patients with refractory or relapsed multiple myeloma treated with SU5416. II. Determine the toxicity of SU5416 in this patient population.

OUTLINE: This is a multicenter study. Patients receive SU5416 IV over 1 hour twice weekly. Treatment continues in the absence of unacceptable toxicity or disease progression. Patients are followed for survival.

PROJECTED ACCRUAL: A total of 20-38 patients will be accrued for this study within 2 years.

研究设计

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

入排标准

年龄范围
18 Years 至 —(Adult, Older 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

研究者

申办方类型
Other
责任方
Sponsor

研究点 (8)

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