跳至主要内容
临床试验/EUCTR2006-000830-11-GB
EUCTR2006-000830-11-GB进行中(未招募)1 期

A randomised prospective trial of tacrolimus-based steroid avoidance in renal transplantation with either alemtuzumab induction or, basiliximab induction and mycophenolate mofetil maintenance therapy - SALAMI

eeds Teaching Hospitals NHS Trust0 个研究点目标入组 120 人开始时间: 2006年4月3日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
120

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Male and female patients who must be over age 18 years.
  • Patients must be recipients of heart-beating cadaveric, non-heart beating or living donors.
  • Patients receiving a 2nd or subsequent grafts must have maintained their primary graft for a minimum of 6 months, except if graft failure was due to technical reasons.
  • Written Informed consent
  • Women at risk of pregnancy must have a negative pregnancy test before commencing the trial and agree to use a medically acceptable method of contraception throughout the treatment period and for 3 months after discontinuing the trial. The manufacturer of Alemtuzumab advises effective contraception for 6 months after administration to men or women. Advice will be given to patients to discuss with the transplant medical staff if a pregnancy is planned.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Regional patients from Hull Royal Infirmary (due to the logistical difficulties in following these patients up from Leeds).
  • High Risk Recipients - defined as recipients who have one or more of the following; 2 HLA-DR mismatch, previous immunologically mediated graft loss in less than 6 months, Preoperative donor specific antibodies
  • Known hypersensitivity to the IMP including the standard drugs.
  • Prohibited prior or concomitant medications
  • Pregnant women or nursing mothers.
  • WBC count < 3000/mm3 or platelets < 75,000/mm3 at time of study entry
  • Any other concurrent cardiovascular, gastrointestinal, pulmonary or haematological conditions that would restrict the administration of study drugs in the opinion of the investigator.

研究者

发起方
eeds Teaching Hospitals NHS Trust

相似试验