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临床试验/NCT00204516
NCT00204516
已完成
1 期

Pilot Study of Intradermal Vaccination of Melanoma Patients With a Fixed Combination of mRNAs Compared to an Individualized Selection After Analysis of Antigen Expression in Tumor Tissue

University Hospital Tuebingen1 个研究点 分布在 1 个国家目标入组 31 人2007年4月

概览

阶段
1 期
干预措施
mRNA coding for melanoma associated antigens
疾病 / 适应症
Malignant Melanoma
发起方
University Hospital Tuebingen
入组人数
31
试验地点
1
主要终点
Tolerability
状态
已完成
最后更新
13年前

概览

简要总结

The purpose of the vaccination protocol is to induce specific immune responses against melanoma associated antigens by intradermal injections of mRNA coding for the corresponding antigen.

详细描述

vaccination protocol to induce clinically specific immune responses against melanoma associated antigens by intradermal injections of mRNA coding for the corresponding antigens. Half of patients is treated with mRNA coding for Melan-A, Mage-A1, Mage-A3, Survivin, GP100 and Tyrosinase. The other half of patients is treated with an individualized selection of mRNAs after analysis of overexpressed melanoma antigens in autologous tumor tissue. GM-CSF is used as an adjuvants. Phase I/II clinical trial to analyse safety and immune responses in stage III/IV melanoma patients.

注册库
clinicaltrials.gov
开始日期
2007年4月
结束日期
2012年12月
最后更新
13年前
研究类型
Interventional
研究设计
Single Group
性别
All

研究者

责任方
Principal Investigator
主要研究者

Thomas Eigentler

Study Coordinator

University Hospital Tuebingen

入排标准

入选标准

  • malignant melanoma stage III/IV
  • fresh frozen tumor tissue available
  • informed consent given
  • Karnofsky \>= 70%

排除标准

  • brain metastasis
  • parallel chemotherapy
  • systemic treatment with glucocorticoids
  • other malignancies

研究组 & 干预措施

mRNA Vacc

干预措施: mRNA coding for melanoma associated antigens

mRNA Vacc

干预措施: GM-CSF

结局指标

主要结局

Tolerability

时间窗: every 4 weeks

Side effects will be monitored using CTCAE criteria. Tolerability and toxicity profiles will be calculated.

研究点 (1)

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