EUCTR2005-005335-94-NL进行中（未招募）1 期
A TREATMENT PROTOCOL FOR PATIENTS CONTINUING FROM A PRIOR SU011248 PROTOCO
Pfizer BV0 个研究点开始时间: 2006年8月10日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
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. Partecipated ina 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 would impart, in the judgment of the investigator, excess risk
- •associated with study participation or study drug administration, or which, in the
- •judgment of the investigator, would make the patient inappropriate for entry
- •into this study
研究者
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