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临床试验/EUCTR2007-004406-26-BE
EUCTR2007-004406-26-BE进行中(未招募)不适用

Comparison of M-Vax plus Low Dose Interleukin-2 versus Placebo Vaccine plus Low Dose Interleukin-2 in patients with Stage IV Melanoma - BB-IND #10658

AVAX Technologies Inc.0 个研究点目标入组 387 人开始时间: 2007年9月4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
387

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

  • - Stage IV metastatic melanoma of cutaneous or mucosal origin or without known primary site
  • - At least one metastatic mass that is surgically resectable, excluding metastases in brain, bowel, or bone
  • - Successful preparation of a vaccine that meets quality control release criteria
  • 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

  • - Failure to prepare a vaccine that meets all quality control release criteria
  • - Uveal melanoma
  • - Brain metastases, current or past (unless successfully treated at least one year prior to enrolment)
  • - Known gentamicin allergy

研究者

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