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临床试验/RPCEC00000358
RPCEC00000358招募中未知

Assessment of the impact of Biomodulina T at the conclusion of first-line chemotherapy in patients diagnosed with non-small cell lung cancer, on the proportion of CD4+ T cells and terminally differentiated CD8+CD28 T cells, as well as the evaluation of these cell populations as possible biomarkers of the CIMAvax-EGF vaccine efficacy - BT- CIMAvax-EGF-NSCLC

Center of Molecular Immunology (CIM)0 个研究点开始时间: 2021年3月18日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
N/a: Single Arm Study. Masking: Open. Control Group: Uncontrolled. Assignment: Single Group. Purpose: Treatment

入排标准

年龄范围
18 years 至 one(—)
性别
All

入选标准

  • 1. Patients of any sex and age over or equal to 18 years old.
  • 2. Patients diagnosed with cyto/histological carcinoma of non-small lung cells in all stages IIIb and IV
  • 3. Patients who have signed informed consent for research
  • 4. Patients with clinical status criteria (ECOG) from 0 to 2

排除标准

  • 1. Patients of childbearing potential who are not using an appropriate method of contraception (intrauterine devices, hormonal contraceptives, barrier methods or tubal ligation). In case of male sex (vasectomy, condom use) for the duration of treatment.
  • 2. Pregnant, lactating or post-breastfeeding patients.

研究者

发起方
Center of Molecular Immunology (CIM)

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