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临床试验/NL-OMON41689
NL-OMON41689已完成3 期

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

Stichting Kinderoncologie Nederland0 个研究点目标入组 34 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
34

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
2 至 17(—)

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

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
Stichting Kinderoncologie Nederland

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