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临床试验/NCT00064376
NCT00064376已完成2 期

A Phase II Trial Of Paricalcitol In Myelodysplastic Syndromes

Cedars-Sinai Medical Center2 个研究点 分布在 1 个国家开始时间: 2003年5月最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
试验地点
2

研究概览

简要总结

RATIONALE: Paricalcitol is a form of vitamin D that may help myelodysplastic cells develop into normal bone marrow cells.

PURPOSE: Phase II trial to study the effectiveness of paricalcitol in treating patients who have myelodysplastic syndrome.

详细描述

OBJECTIVES:

  • Determine the clinical effects of paricalcitol in patients with myelodysplastic syndromes.
  • Determine whether this drug can improve RBC, WBC, or platelet counts in these patients.
  • Determine whether this drug can decrease the risk of development of leukemia without causing undue toxicity in these patients.

OUTLINE: Patients receive oral paricalcitol daily for 4 months in the absence of disease progression or unacceptable toxicity.

Patients are followed at 1 month.

PROJECTED ACCRUAL: A total of 20 patients will be accrued for this study within 8 months.

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
25 Years 至 100 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

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

H. Phillip Koeffler

Director, Medicine / Hematology/Oncology

Cedars-Sinai Medical Center

研究点 (2)

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