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临床试验/NCT01433770
NCT01433770撤回不适用

Effects of Alefacept on Donor-Specific Memory in Kidney Transplant Recipients

University Hospitals Cleveland Medical Center1 个研究点 分布在 1 个国家开始时间: 2011年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
撤回
试验地点
1
主要终点
Absolute changes in ELISPOTS, PRT (Panel Reactive T Cells), and lymphocyte subsets will be analyzed using paired t-tests to compare baseline vs 4, 8, 12, 16, and 24 weeks of follow-up

研究概览

简要总结

Alefacept, also known as Amevive®, is a medication approved by the Food and Drug Administration (FDA) in the United States and other countries for the treatment of psoriasis, which is a chronic inflammatory immunological skin condition that can result in chronic dry, red patches that are covered in scales. Alefacept is approved by the FDA for the treatment of psoriasis but not as an anti-rejection medication in transplant patients. It is now being tested in new kidney transplant patients as a supplement to other approved anti-rejection drugs. Alefacept will be used as an investigational drug in this study.

The reason for this study is to test whether using Alefacept will inhibit T cells, known as memory cells, using a test named ELISPOT-IFN. In patients with psoriasis, Alefacept inhibits these memory cells. If memory cells specific to your donor can be inhibited by this drug, it might prevent rejection and promote acceptance of the transplanted kidney in a unique manner.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Able and willing to sign informed consent
  • Adult (>18years) kidney-alone transplant recipient
  • 6 months post-transplant
  • Persistently positive donor-stimulated ELISPOT-IFN (≥30 spots/300K cells)-2 positive assays separated by at least one week
  • Female subjects of child bearing potential must have a negative urine or serum pregnancy test within 7 days prior to enrollment and must agree to maintain effective birth control during the study

排除标准

  • Baseline CD4 count <250 cells/uL
  • Acute rejection episode within the 3 months prior to enrollment
  • Clinically overt infection within the 3 months prior to enrollment
  • History of BK polyoma viremia
  • Recipient or donor is known to be seropositive for human immunodeficiency virus (HIV)
  • Subject has a current malignancy or a history of malignancy (within the past 5 years), except non-metastatic basal or squamous cell carcinoma of the skin that has been treated successfully
  • Any major illnesses/condition that, in the investigator's judgment, will substantially increase the risk associated with the subject's participation in and completion of the study, or could preclude the evaluation of the subject's response

研究组 & 干预措施

Alefacept action on memory T cells

Experimental

干预措施: Amevive (Drug)

结局指标

主要结局

Absolute changes in ELISPOTS, PRT (Panel Reactive T Cells), and lymphocyte subsets will be analyzed using paired t-tests to compare baseline vs 4, 8, 12, 16, and 24 weeks of follow-up

时间窗: 12, 24, and 36 months

次要结局

  • The incidence of clinically overt infections will be descriptive or calculated as a simple percentage.(12, 24, and 36 months)

研究者

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

Donald Hricik

Professor of Medicine, Chief Division of Nephrology and Hypertension, Medical Director Transplantation Services

University Hospitals Cleveland Medical Center

研究点 (1)

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