跳至主要内容
临床试验/NCT00050843
NCT00050843已完成3 期

A Study to Access the Safety/Efficacy of Thalidomide in the Treatment of Anemia in Patients With Myelodysplastic Syndromes

Celgene Corporation38 个研究点 分布在 1 个国家目标入组 220 人开始时间: 2001年8月1日最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
220
试验地点
38

研究概览

简要总结

The primary objective of the study is to determine the efficacy of thalidomide for the treatment of anemia in patients with myelodysplastic syndromes (MDS).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Eligible patients must have a diagnosis of myelodysplastic syndrome
  • •Life expectancy of at least 6 months.
  • •Patients must be able to adhere to the study visit schedule and other protocol requirements.
  • •Patients must understand and voluntarily sign an informed consent document.
  • •Women of childbearing potential (WCBP) must agree to practice abstinence or to use TWO methods of contraception beginning 4 weeks prior to the start of study medication and throughout the course of treatment.
  • •Males must use barrier contraception when engaging in reproductive sexual activity with women of childbearing potential.

排除标准

  • 未提供

研究者

申办方类型
Industry

研究点 (38)

Loading locations...

相似试验

A Study to Access the Safety/Efficacy of Thalidomide... | 临床试验