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临床试验/NCT00482495
NCT00482495已完成2 期

A Phase II Trial of Bevacizumab in Patients With Relapsed or Refractory Multiple Myeloma

Mayo Clinic2 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2006年4月最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
Mayo Clinic
入组人数
42
试验地点
2
主要终点
Confirmed hematologic response

研究概览

简要总结

RATIONALE: Monoclonal antibodies, such as bevacizumab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or carry cancer-killing substances to them. Bevacizumab may also stop the growth of multiple myeloma by blocking blood flow to the cancer.

PURPOSE: This phase II trial is studying how well bevacizumab works in treating patients with relapsed or refractory multiple myeloma.

详细描述

OBJECTIVES:

Primary

  • Determine the hematologic response rate in patients with relapsed or refractory multiple myeloma treated with bevacizumab.
  • Determine the proportion of patients who are progression free and have not failed treatment after 1 year.

Secondary

  • Determine the toxicity of this drug in these patient.
  • Determine the time to disease progression in patients receiving this drug.
  • Determine the overall survival and survival at 1 year in patients receiving this drug.

研究设计

研究类型
Interventional
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

Confirmed hematologic response

Progression-free survival at 1 year

次要结局

  • Toxicity as measured by NCI CTCAE v3.0
  • Time to progression
  • Duration of response
  • Survival

研究者

发起方
Mayo Clinic
申办方类型
Other

研究点 (2)

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