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临床试验/EUCTR2006-001247-64-SE
EUCTR2006-001247-64-SE进行中(未招募)不适用

An open label, stratified, single-arm phase II study of RAD001 in patients with advanced pancreatic neuroendocrine tumor (NET) after failure of cytotoxic chemotherapy - NA

ovartis Pharma Services AG0 个研究点目标入组 144 人开始时间: 2006年5月12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)
入组人数
144

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

  • Advanced (unresectable or metastatic) biopsy-proven pancreatic NET
  • Confirmed low-grade or intermediate-grade neuroendocrine carcinoma
  • Objective disease progression by RECIST criteria while receiving cytotoxic chemotherapy or at any time after receiving an adequate course of cytotoxic chemotherapy (i.e., at least 3 consecutive cycles or months of treatment with the same cytotoxic drug or regimen)
  • Presence of at least one measurable disease using RECIST criteria at screening (CT or MRI)
  • Adequate bone marrow, liver and kidney function Other protocol-defined inclusion criteria may apply
  • 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

  • Patients with poorly differentiated neuroendocrine carcinoma
  • Hepatic artery embolization within the last 6 months
  • Prior therapy with everolimus or other rapamycins (sirolimus, temsirolimus)
  • Other concurrent malignancy
  • Other serious intercurrent infections or nonmalignant uncontrolled medical illnesses Other protocol-defined exclusion criteria may apply

研究者

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