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临床试验/NCT00040469
NCT00040469终止2 期

Allogeneic Bone Marrow Transplant From HLA Identical Related Donors for Patients With High Risk Hemoglobinopathies: Hemoglobin SS, Hemoglobin SC, Hemoglobin SB0/+ Thalassemia, or Homozygous B0/+ Thalassemia or Severe Variants of B0/+ Thalassemia

Baylor College of Medicine2 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2000年8月1日最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
终止
入组人数
15
试验地点
2

研究概览

简要总结

The major goal of this study is to determine the risks and benefits of bone marrow transplants in patients with severe thalassemia or sickle cell disease. Participation in this project will be for two years.

详细描述

To do the bone marrow transplant, we must first kill the cells in the bone marrow that make the abnormal red blood cells that are found in patients with severe thalassemia or sickle cell disease.

We will do this by using three drugs: busulfan, cyclophosphamide, and CAMPATH-1H. CAMPATH-IH is an investigational drug. CAMPATH-1H is used to prevent participants from rejecting or refusing to let the donor blood cells grow in the body. After the drug treatment, participants will be given bone marrow from a brother or sister who has healthy bone marrow that matches.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
1 Day 至 64 Years(Child, Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients with homozygous B0/+ thalassemia or severe variants of B0/+ thalassemia with an HLA genotypically identical donor.
  • •Patients with an HLA genotype identical donor and hemoglobin SS, hemoglobin SC, or hemoglobin Sb 0/+ and at least one of the following:
  • •Previous central nervous system vaso-occlusive episode with or without residual neurologic findings; Frequent painful vaso-occlusive episodes which significantly interfere with normal life activities and which necessitate chronic transfusion therapy; Recurrent SCD chest syndrome events which necessitate chronic transfusion therapy.
  • •Severe anemia which prevents acceptable quality of life and necessitates chronic transfusion therapy.
  • •The patient must have an HLA genotype identical donor.
  • •Between the ages of birth and 65 years.
  • •Women of childbearing potential must have a negative pregnancy test.

排除标准

  • •Biopsy proven chronic active hepatitis or fibrosis with portal bridging.
  • •SCD chronic lung disease >/= stage
  • •Severe renal dysfunction defined as creatinine clearance <40 ml/min/1.73 M2
  • •Severe cardiac dysfunction defined as shortening fraction <25%.
  • •HIV infection.
  • •Severe but unspecified chronic toxicity serious enough to detrimentally affect the patient's capacity to tolerate bone marrow transplant (BMT).
  • •Inadequate intellectual capacity to understand the nature and risk inherent in the BMT process and give informed consent (in the case of minors, this criteria must be fulfilled by the legal guardian).
  • •Pregnant, lactating or unwilling to use appropriate birth control.

研究者

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

Robert Krance

Professor

Baylor College of Medicine

研究点 (2)

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