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临床试验/NCT01154439
NCT01154439已完成1 期

A Phase I Study Investigating the Combination of RAD001 With Standard Induction and Consolidation Therapy in Older Patients With Newly Diagnosed Acute Myeloid Leukemia (AML)

Gruppo Italiano Malattie EMatologiche dell'Adulto5 个研究点 分布在 1 个国家目标入组 11 人开始时间: 2010年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
11
试验地点
5
主要终点
Maximum-tolerated dose of everolimus

研究概览

简要总结

RATIONALE: Drugs used in chemotherapy, such as mitoxantrone hydrochloride, cytarabine, etoposide, and idarubicin, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Everolimus may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the cancer. Giving everolimus together with combination chemotherapy may kill more cancer cells.

PURPOSE: This phase I trial is studying the side effects and best dose of everolimus when given together with mitoxantrone hydrochloride, cytarabine, etoposide, and idarubicin in treating older patients with newly diagnosed acute myeloid leukemia.

详细描述

OBJECTIVES:

Primary

  • To determine the maximum-tolerated dose of everolimus in combination with standard remission-induction therapy comprising mitoxantrone hydrochloride, cytarabine, and etoposide (MICE-regimen) followed by consolidation therapy comprising idarubicin, cytarabine, and etoposide in older patients with newly diagnosed acute myeloid leukemia.

Secondary

  • To determine the safety profile of this regimen in these patients.
  • To determine the anti-leukemic activity (complete remission rate [complete remission and complete remission with incomplete blood count recovery]) following one or two induction courses.

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
61 Years 至 75 Years(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

Everolimus

Experimental

Everolimus mice-regimen

干预措施: cytarabine (Drug)

Everolimus

Experimental

Everolimus mice-regimen

干预措施: etoposide (Drug)

Everolimus

Experimental

Everolimus mice-regimen

干预措施: everolimus (Drug)

Everolimus

Experimental

Everolimus mice-regimen

干预措施: idarubicin (Drug)

Everolimus

Experimental

Everolimus mice-regimen

干预措施: mitoxantrone hydrochloride (Drug)

结局指标

主要结局

Maximum-tolerated dose of everolimus

时间窗: At one year from study entry

MTD of RAD given in combination with the MICE regimen

次要结局

  • Safety(At one year from study entry)
  • Complete remission rate(At one year from study entry)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (5)

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