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临床试验/NCT00074048
NCT00074048已完成2 期

Phase II Trial Of BL22 Immunotoxin In Hairy Cell Leukemia

MedImmune LLC1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2003年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
MedImmune LLC
入组人数
36
试验地点
1
主要终点
Response rate

研究概览

简要总结

RATIONALE: The BL22 immunotoxin can locate tumor cells and kill them without harming normal cells. This may be an effective treatment for hairy cell leukemia that has not responded to treatment with cladribine.

PURPOSE: This phase II trial is studying BL22 immunotoxin to see how well it works in treating patients previously treated with cladribine for hairy cell leukemia.

详细描述

OBJECTIVES:

Primary

  • Determine the response rate in patients with cladribine-resistant hairy cell leukemia treated with BL22 immunotoxin.

Secondary

  • Determine the response duration in patients treated with this drug.
  • Determine the safety of this drug in these patients.
  • Determine the pharmacokinetics of this drug in these patients.
  • Correlate BL22 blood levels and toxicity of this drug with the development of neutralizing antibodies in these patients.

研究设计

研究类型
Interventional
分配方式
Non Randomized
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

研究组 & 干预措施

1

Experimental

BL22 immunotoxin

干预措施: BL22 (Drug)

结局指标

主要结局

Response rate

时间窗: After even cycle numbers (2,4,6,8,10)

次要结局

  • Duration of Response: [Timeframe: Date that a response begins with the date that PD is documented.](30 days after last dose of study drug)

研究者

发起方
MedImmune LLC
申办方类型
Industry

研究点 (1)

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