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临床试验/NCT00462189
NCT00462189Unknown1 期

A Phase 1, Multicenter, Dose Escalation Study of CAT-8015 in Patient With Relapsed or Refractory Hairy Cell Leukemia (HCL)

Cambridge Antibody Technology8 个研究点 分布在 3 个国家目标入组 40 人开始时间: 2007年4月最近更新:
适应症
相关药物

试验速览

阶段
1 期
入组人数
40
试验地点
8
主要终点
Estimate the maximum dose that can be safely administered to a patient

研究概览

简要总结

RATIONALE: The CAT-8015 immunotoxin can bind tumor cells and kill them without harming normal cells. This may be an effective treatment for hairy cell leukemia(HCL) that has not responded to chemotherapy, surgery or radiation therapy.

PURPOSE: Phase I dose escalation study to determine the maximum tolerated dose of CAT-8015 immunotoxin in treating patients who have hairy cell leukemia (HCL) that has not responded to treatment.

详细描述

OUTLINE: Patients receive CAT-8015 IV over 30 minutes on days 1, 3, and 5 followed by rest. Treatment repeats every 4 weeks for up to a total of 10 courses in the absence of dose limiting toxicity, complete response or disease progression. Patients are followed at 1, 3, 6,12,15,18, 21, 24 months following the start of the last treatment cycle.

Cohorts of 3-6 patients each will receive escalating doses of recombinant CAT-8015 until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose proceeding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity. Once the MTD is determined, between16 to 25 new patients will be added to the MTD cohort depending on how well the CAT-8015 is tolerated.

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

结局指标

主要结局

Estimate the maximum dose that can be safely administered to a patient

Characterize the toxicity profile of CAT-8015

Study the clinical pharmacology of CAT-8015

Observe anti-tumor activity, if any.

次要结局

  • To assess the immunogenic potential of CAT-8015 to induce antibodies
  • To investigate the potential of biomarkers to predict any therapeutic or toxic response.

研究者

申办方类型
Other

研究点 (8)

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