EUCTR2005-005335-94-DE进行中（未招募）不适用
A TREATMENT PROTOCOL FOR PATIENTS CONTINUING FROM A PRIOR SU011248 PROTOCO
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 入组人数
- 300
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
- •1. Participated in a previous SU011248 protocol and are judged by the investigator
- •to have the potential to derive clinical benefit from SU011248 treatment
- •2. Signed and dated informed consent document indicating that the patient (or
- •legally acceptable representative) has been informed of all the pertinent aspects
- •of the trial prior to enrollment.
- •3. Enrollment within 8 weeks from their last dose of SU011248 or placebo in their
- •previous study.
- •4. Willingness and ability to comply with scheduled visits, treatment plans and
- •laboratory tests and other study procedures.
- •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
- •Subjects presenting with any of the following will not be included in the trial:
- •1. Current treatment in another clinical trial
- •2. Pregnancy or breastfeeding
- •3. Severe acute or chronic medical or psychiatric condition, or laboratory
- •abnormality that may increase the risk associated with study participation or
- •study drug administration, or may interfere with the interpretation of study
- •results, and in the judgement of the investigator would make the patient
- •inappropriate for entry into this study
- •4. Left ventricular ejection fraction (LVEF) <50% as assessed by MUGA or ECHO
研究者
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