EUCTR2005-005335-94-IT进行中（未招募）不适用
A TREATMENT PROTOCOL FOR PATIENTS CONTINUING FROM A PRIOR SU011248 PROTOCOL - ND
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- PFIZER
- 入组人数
- 500
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 SU011248 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
- •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 judgment of the investigator would make the patient inappropriate for entry into this study.
研究者
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A Treatment Protocol for Patients Continuing from a Prior SU011248 ProtocolThis is an open-label treatment protocol for patients who have participated in other SU011248 protocols to completion and are believed to have the potential to derive clinical benefit from SU011248 treatment. Included in this protocol will be patients assigned to placebo in a previous study who did not qualify for crossover within the original protocol due to declining health status (eg, performance status lower than crossover eligibility criterionMedDRA version: 7.1Level: LLYClassification code 10062427EUCTR2004-001093-11-SEPfizer Ltd