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临床试验/NCT00002745
NCT00002745已完成2 期

PHASE II STUDY OF 9-AMINOCAMPTOTHECIN (9-AC/DMA, NSC# 603071) IN PREVIOUSLY TREATED HODGKIN'S DISEASE AND NON-HODGKIN'S LYMPHOMA: IWF GRADES A-H

National Cancer Institute (NCI)5 个研究点 分布在 1 个国家目标入组 37 人开始时间: 1996年4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
入组人数
37
试验地点
5
主要终点
Response

研究概览

简要总结

Phase II trial to study the effectiveness of aminocamptothecin in treating patients who have refractory or recurrent Hodgkin's disease or non-Hodgkin's lymphoma. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die.

详细描述

OBJECTIVES:

I. Evaluate the response rate and duration of response to aminocamptothecin (9-AC) in patients with refractory or relapsed Hodgkin's disease or non-Hodgkin's lymphoma.

II. Assess the toxicity of 9-AC in these patients. III. Validate a preliminary pharmacodynamic model relating total 9-AC concentration, albumin, and bilirubin to toxicity.

IV. Determine whether 9-AC concentrations correlate with response.

OUTLINE: Patients are stratified by disease histology (International Working Formulation (IWF) A-C vs IWF D-F) and center.

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

研究组 & 干预措施

aminocamptothecin

Experimental

aminocamptothecin

干预措施: aminocamptothecin (Drug)

结局指标

主要结局

Response

时间窗: 2 years post treatment

次要结局

  • Toxicity(day 1 of each cycle)
  • 9-AC/DMA concentrations(Pre-treatment cycle 1 and just prior to completion of cycle 1)

研究者

申办方类型
Nih
责任方
Sponsor

研究点 (5)

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