NCT00240214终止不适用
An Open Label Post Marketing Surveillance Assessment to Evaluate the Effectiveness and Safety of Rapamune in Patients After Kidney Transplantation Receiving a Rapamune Containing Regime
Wyeth is now a wholly owned subsidiary of Pfizer0 个研究点目标入组 500 人开始时间: 2001年4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
- 终止
- 发起方
- 入组人数
- 500
研究概览
简要总结
The purpose of this study is to obtain data on the effectiveness and safety of Rapamune under everyday conditions
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients having received a renal allograft from a cadaveric or living donor with low or moderate risk of developing acute rejection episodes.
排除标准
- •Contraindications according to Summary of the Product Characteristics (SmPC).
研究组 & 干预措施
1
sirolimus
干预措施: sirolimus (Drug)
研究者
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