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临床试验/EUCTR2004-002925-39-SE
EUCTR2004-002925-39-SE进行中(未招募)不适用

A Phase II study of Temozolomide (Temodal) Given Continously 100mg/m2 for 21 Days in 28 Day cycles in Patients with Metastatic Melanoma.

Kliniken för onkologi, Karolinska Universitetssjukhuset, Solna0 个研究点目标入组 35 人开始时间: 2004年12月22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
入组人数
35

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 melanoma
  • Evidence of metastatic disease with at least one mesurable metastatic site
  • Performance status WHO 0-2
  • Age >18 years
  • 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) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Prior chemotherapy, biologic therapy or immunotherapy for metastatic disease
  • Evidence of brain metases
  • Frequent vomiting or medical condition which could interfere with oral medication intake
  • Any other active malignancies or previous malignancies within the last 5 years
  • Pregnancy or breast feeding

研究者

发起方
Kliniken för onkologi, Karolinska Universitetssjukhuset, Solna

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