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临床试验/NCT00167661
NCT00167661终止1 期

Campath-1H Induction to Allow Steroid Free Immunosuppression in Pediatric Renal Transplantation

University of Wisconsin, Madison1 个研究点 分布在 1 个国家目标入组 33 人开始时间: 2004年6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
终止
入组人数
33
试验地点
1
主要终点
Incidence of Graft Rejection

研究概览

简要总结

The purpose of this study is to determine whether Campath-1H induction and the associated lymphocyte depletion will permit long-term rejection-free renal allograft survival in the absence of ongoing corticosteroid administration.

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
18 Months 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Participants must be a single-organ recipient (kidney only)
  • Participants who are receiving their first living donor or deceased donor transplant

排除标准

  • Participants who are recipients of HLA-identical living-donor renal transplants
  • Participants with a PRA value > 10% within 30 days prior to the transplant
  • Participants who have received a multi-organ transplant
  • Participants who are who are positive for hepatitis C, hepatitis B surface antigen or HIV
  • Participants who have received an investigational drug within 6 weeks of study entry
  • Participants who have a previous history of, or who currently have, malignancies and/or lymphoma
  • Participants who have received corticosteroids within three months of transplantation
  • Participants who are 3rd transplant recipients
  • Female participants who are pregnant or lactating. Fertile female participants who are sexually active must agree to use an acceptable method of birth control during the study

研究组 & 干预措施

Campath 1-H

Experimental

Campath 1-H

干预措施: Campath-1H (Drug)

结局指标

主要结局

Incidence of Graft Rejection

时间窗: at 1, 3, 6, 12, and 24 months

Participant Graft Survival

时间窗: at 6, 12, and 24 months

次要结局

  • Number of Participants With Hypertension(up to 24 months)
  • Number of Participants With Hyperlipidemia(up to 24 months)
  • Participant Survival(at 6, 12, and 24 months)
  • Number of Participants With Malignancy(up to 24 months)
  • Number of Participant With Diabetes Mellitus(up to 24 months)
  • Estimated Glomerular Filtration Rate (EGFR)(at 1, 6, 12 and 24 months)
  • Number of Participants With Infection(up to 24 months)
  • Growth Post-transplant Reported by Height Z Score(up to 24 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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