EUCTR2005-001830-34-GB进行中（未招募）1 期
The use of Myfortic in paediatric patients after liver transplantation
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 4
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
入选标准
- •Group 1: high risk for kidney dysfunction or pre-existing kidney dysfunction (GFR <80 ml/min/1.73m2). This inlcudes but is not limited to childen transplanted for hepatoblastoma, Alagilles syndrome, cystic fibrosis, alpha-1-antitrypsin deficiency, hyperoxuluria. The child is able to swallow tablets whole
- •Group 2: The child is experiencing gastrointestinal side effects of MMF requiring it to be reduced. The child is able to swallow tablets whole.
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) no
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Parental consent and child assent has not been ascertained, pregnancy (all sexually active girls >12 years will have a pregnancy test prior to starting the study drug); hypersensitivity to mycophenolate
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