跳至主要内容
临床试验/EUCTR2011-005968-24-IT
EUCTR2011-005968-24-IT进行中(未招募)不适用

A multicenter, randomized, double-blind, placebo-controlled Phase IIb Efficacy Study of Vx-001, a peptide-based cancer vaccine aimed to maintain disease control after first line treatment in HLA-A*0201 positive patients with TERT positive NSCLC (stage IV or recurrent stage I-III) - VaxLung

VAXON BIOTECH0 个研究点目标入组 150 人开始时间: 2012年8月7日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
VAXON BIOTECH
入组人数
150

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

  • - MF from 18 years of age; - Documented stage IV NSCLC or recurrent stage I-III disease; - Patients treated with 4 cycles platinum based 1st line chemotherapy; - Documented HLA-A*0201 positive; - TERT-positive NSCLC.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range: 0
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 50
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - Mixed small cell and NSCLC histologies; - Patients with stage IV or recurrent NSCLC who have been previously treated with therapy other than platinum-based first-line chemotherapy; - Prior treatment with cancer vaccines; - Prior treatment with immunotherapy within four weeks prior to randomization.

研究者

发起方
VAXON BIOTECH

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