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临床试验/EUCTR2004-003910-41-DE
EUCTR2004-003910-41-DE进行中(未招募)不适用

Pilot Phase II, Open Label, Multicenter, Efficacy and Safety Study of 852A Administered Intravenously to Subjects with Unresectable Metastatic Cutaneous Melanoma - 852A-IV-NA-LI-04-MC-M

3M Health Care Limited0 个研究点目标入组 28 人开始时间: 2005年2月25日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
28

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

  • •Most important inclusion criteria:
  • •Subjects have:
  • •-histological evidence of melanoma
  • •-advanced melanoma not responding to a first line of chemotherapy
  • •-Eastern Cooperative Oncology Group (ECOG) performance status less than or equal to 2
  • •-a life expectancy of greater than or equal to 6 months
  • •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

  • •Most important exclusion criteria:
  • •Subjects are excluded who have:
  • •- had prior immunotherapy for stage IV melanoma (including but not limited to: Interferons, IL-2, TNF alpha and melanoma vaccines) within 6 weeks of the first dose of 852A
  • •- stage IV disease which has previously progressed during treatment with interferon alone or combined interferon and monochemotherapy
  • •-brain metastases with the exception of brain metastases completely excised or
  • •successfully controlled with stereotactic radiosurgery

研究者

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