jRCTs061180058已完成不适用
A phase I study of combination immunotherapy with HSP70 derived peptide, GPC3 derived peptide, IMP321 and Hiltonol for patients with advanced or metastatic solid cancer (A phase I study of combination immunotherapy with HSP70 derived peptide, GPC3 derived peptide, IMP321 and Hiltonol for patients with advanced or metastatic solid cancer)
未提供0 个研究点目标入组 18 人开始时间: 2016年1月12日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 18
- 主要终点
- -
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
- Single Arm Study
- 干预模型
- Single Assignment
- 主要目的
- Treatment Purpose
- 盲法
- Open(masking Not Used)
入排标准
- 年龄范围
- 20age old over 至 No limit(—)
- 性别
- All
入选标准
- •1.patients with advanced or metastatic solid cancer (Pancreatic cancer, colon cancer, gastric cancer, esophageal cancer, liver cancer and breast cancer) proven by histology or imaging (CT or MRI)
- •Patients with HLA-A*2402 -A*0201 -A*0206
- •Standard treatment failure cancer
- •Performance Status (PS); 0-1, Eastern Cooperative
- •Oncology Group (ECOG)
- •Preserved organ functions (number of WBCs more than
- •2.0x103/mm3; % of lymphocyte >=15; number of platelets
- •>=7.5x103/mm3; hemoglobin >=8.0 g/ dl; creatinine <=2.5
- •times of upper normal limit)
- •7.Patients provided written, informed consent to participate
排除标准
- •The exclusion criteria were, double cancer, pneumonitis, severe allergy, severe infection, neurological disturbance, uncontrolled general diseases, heart diseases, general steroid treatment, or any prior therapies using same agents of this study.
结局指标
主要结局
-
safety
次要结局
- Antitumor effect
研究者
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