跳至主要内容
临床试验/EUCTR2005-003867-21-SE
EUCTR2005-003867-21-SE进行中(未招募)不适用

Induction chemotherapy with docetaxel and cisplatin followed by radiotherapy concomitant with cetuximab for locally advanced stage III non-small cell lung cancer- amulticentre, open label non-randomised phase II trial - Satellit

Sahlgrenska University Hospital0 个研究点目标入组 75 人开始时间: 2005年11月24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)
发起方
入组人数
75

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

  • ·Histological or cytological diagnosis of a NSCLC Stage IIIA/IIIB
  • Non- resectable or medically inoperable patients.
  • Received no prior chemotherapy or radiation therapy for NSCLC
  • PS WHO 0 - 1.
  • FEV1 ³ 1L or ³ 40% of expected volume.
  • Adequate bone marrow reserve: WBCC ³ 3.0 ´ 109/L, Platelets ³100 ´ 109/L, Haemoglobin ³100 ml/l .·
  • Age ³18 years, no upper age limit.
  • 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

  • Evidence of active infection at the discretion of the investigator.·
  • Inadequate liver function: Bilirubin >1,5 x UNL, ALAT or ASAT >3,0 UNL·
  • Inadequate kidney function: creatinine >1,5 x UNL or GFR < 50 ml/min.·Pleural effusion with positive cytology·
  • Serious concomitant systemic disorder incompatible with the study.·Second primary malignancy (except in situ carcinoma of the cervix or adequately treated basal cell carcinoma of the skin) unless treated, in remission and off active treatment for greater than 5 years.

研究者

发起方
Sahlgrenska University Hospital

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