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临床试验/NL-OMON42306
NL-OMON42306已完成不适用

Myeloid and plasmacytoid blood dendritic cells for immunotherapy of stage III melanoma patients - myDC/pDC in stage III melanoma patients

Tumor Immunologie0 个研究点目标入组 30 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
30

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
18 至 99(—)

入选标准

  • - stage III melanoma according to the 2009 AJCC criteria
  • - cytological or histological documented evidence of stage III melanoma
  • - WHO performance status 0-1 (Karnofsky 100-70) (Appendix 1)
  • - life expectancy *3 months
  • - age 18-75 years
  • - WBC >3.0×109/l, lymphocytes >0.8×109/l, platelets >100×109/l,
  • serum creatinine <150 µmol/l, serum bilirubin <25 µmol/l
  • - normal serum LDH (*250 U/l)
  • - expected adequacy of follow-up
  • - no pregnant or lactating women
  • - written informed consent

排除标准

  • - irresectable stage III melanoma or stage IV melanoma
  • - any concurrent adjuvant therapy
  • - history of any second malignancy in the previous 5 years, with the exception of adequately treated basal cell carcinoma or carcinoma in situ of the cervix
  • - serious active infections, known HbsAg or HIV positive, or autoimmune diseases or organ allografts
  • - concomitant use of oral immunosuppressive drugs
  • - known allergy to shell fish (since it contains KLH)
  • - any serious clinical condition that may interfere with the safe administration of DC or apheresis

研究者

发起方
Tumor Immunologie

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