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临床试验/NCT00798889
NCT00798889已完成不适用

A Treatment Protocol For Patients Continuing From A Prior SU011248 Protocol

Pfizer1 个研究点 分布在 1 个国家目标入组 314 人开始时间: 2004年3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
已完成
发起方
Pfizer
入组人数
314
试验地点
1
主要终点
Duration of Treatment

研究概览

简要总结

The objective of this protocol is to provide SU011248 treatment for patients who have participated in a SU011248 protocol and are eligible to enter this protocol

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Prior SU011248 Protocol.
  • Eligible to continue SU011248 treatment.

排除标准

  • Uncontrolled CNS metastasis.
  • Unfit to receive SU011248.

研究组 & 干预措施

Sunitinib

Experimental

干预措施: Sunitinib (Drug)

结局指标

主要结局

Duration of Treatment

时间窗: Baseline up to Day 28 after last dose of study treatment

次要结局

未报告次要终点

研究者

发起方
Pfizer
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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