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临床试验/EUCTR2009-010672-16-IT
EUCTR2009-010672-16-IT进行中(未招募)不适用

PHASE II STUDY OF SUNITINIB IN METASTATIC RENAL CANCER WITH NON-CLEAR CELL HISTOLOGY - ONC-2008-004

ISTITUTO CLINICO HUMANITAS0 个研究点开始时间: 2009年11月24日最近更新:
适应症
相关药物

试验速览

阶段
不适用
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

  • Histologically proven diagnosis of NCCRC (papillary or cromophobe), confirmed by a central review of an expert pathologist. No previous treatment. Age superior to 18 years. ECOG Performance Status 0-2. Life expectancy of at least 12 weeks. Measurable lesions according to RECIST criteria. Adequate cardiac, hepatic, renal, and bone marrow function. Written informed consent.
  • 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

  • Prior treatment with an antiangiogenetic compound. Symptomatic and/or unstable pre-existing brain metastases. Uncontrolled hypertension. Severe or uncontrolled cardiovascular diseases (congestive heart failure, myocardial infarction) within 6 months of study. Active uncontrolled infections. Other co-existing malignancies or malignancies diagnosed within the last 5 years with the exception of basal cell carcinoma or cervical cancer in situ.

研究者

发起方
ISTITUTO CLINICO HUMANITAS

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