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临床试验/EUCTR2008-000582-39-SK
EUCTR2008-000582-39-SK进行中(未招募)1 期

An Open label single arm trial investigating zalutumumab, a Human Monoclonal Anti-EGF receptor Antibody, in combination with Best Supportive Care, in Patients with Non-Curable Squamous Cell Carcinoma of the Head and Neck who have Failed Standard Platinum-based Chemotherapy. - Zalutumumab in non-curable Patients with SCCH

Genmab A/S0 个研究点目标入组 100 人开始时间: 2008年6月19日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
Genmab A/S
入组人数
100

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

  • 1. Squamous cell carcinoma of the oral cavity, oropharynx, hypopharynx or larynx, considered incurable with standard therapy
  • 2. Patients must have disease progression according to RECIST.
  • 3. Measurable disease defined as one or more target lesions according to RECIST.
  • 4. WHO PS =2
  • 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

  • 1. Three or more prior chemotherapy regimens other than platinum based chemotherapy.
  • 2. Prior treatment with EGFr antibodies and/or EGFr small molecule inhibitors unless given as part of first line treatment of locally or regionally advanced SCCHN in combination with chemotherapy and/or radiotherapy. Exposure to EGFr targeted therapy must be completed = 6 weeks prior to visit 2
  • 3. Received the following treatments within 4 weeks prior to Visit 2:
  • - Cytotoxic or cytostatic anti-cancer chemotherapy
  • - Total tumor resection

研究者

发起方
Genmab A/S

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