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临床试验/EUCTR2006-000995-33-NL
EUCTR2006-000995-33-NL进行中(未招募)1 期

EuroNet-Paediatric Hodgkin?s Lymphoma Group First international Inter-Group Study for classical Hodgkin?s Lymphoma in Children and Adolescents - EuroNet-PHL-C1

Martin-Luther-University Halle-Wittenberg0 个研究点目标入组 1,200 人开始时间: 2010年9月20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
入组人数
1,200

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

入选标准

  • ?diagnosis of classic Hodgkin?s lymphoma
  • ?patient aged under 18 years at time of diagnosis
  • ?written informed consent of the patient and/or the patient?s parents or guardian according to national laws
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) no
  • 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

  • ?pre-treatment of Hodgkin?s lymphoma differing from study protocol (except recommended pre-phase therapy of a large mediastinal tumour)
  • ?known hypersensitivity or contraindication to study drugs
  • ?diagnosis of lymphocyte predominant Hodgkin?s lymphoma
  • ?prior chemotherapy or radiotherapy
  • ?other (simultaneous) malignancies
  • ?pregnancy and / or lactation
  • ?females who are sexually active refusing to use effective contraception (oral contraception, intrauterine devices, barrier method of contraception in conjunction with spermicidal jelly or surgical sterile)
  • ?Current or recent (within 30 days prior to start of trial treatment) treatment with another investigational drug or participation in another investigational trial
  • ?severe concomitant diseases (e.g. immune deficiency syndrome)
  • ?known HIV positivity

研究者

发起方
Martin-Luther-University Halle-Wittenberg

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