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临床试验/NCT00001705
NCT00001705已完成2 期

Immunization of Patients With Metastatic Melanoma Using the GP100 Peptide Preceded by an Endoplasmic Reticulum Insertion Signal Sequence

National Cancer Institute (NCI)1 个研究点 分布在 1 个国家目标入组 141 人开始时间: 1998年7月1日最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
141
试验地点
1

研究概览

简要总结

Patients with metastatic melanoma who are HLA-A201+ will be immunized with a modified peptide from the gp100 molecule that contains a signal sequence designed to improve peptide presentation by antigen presenting cells. This peptide called gp100:ES209-217 (210M) will be administered either alone or in combination with high or low dose IL-2. Patients will be evaluated for clinical response, as well as undergo studies of the immunologic response to the peptide immunization.

详细描述

Patients with metastatic melanoma who are HLA-A201+ will be immunized with a modified peptide from the gp100 molecule that contains a signal sequence designed to improve peptide presentation by antigen presenting cells. This peptide called gp100:ES209-217 (210M) will be administered either alone or in combination with high or low dose IL-2. Patients will be evaluated for clinical response, as well as undergo studies of the immunologic response to the peptide immunization.

研究设计

研究类型
Interventional
主要目的
Treatment

入排标准

性别
All
接受健康志愿者
否

入选标准

  • •Any patient age greater than or equal to 18 with measurable metastatic melanoma who has failed standard treatment and has an expected survival of greater than three months will be considered.
  • •Serum creatinine of 2.0 mg/dl or less.
  • •Bilirubin 1.6 mg/dl or less.
  • •WBC 3000/mm(3) or greater.
  • •Platelet count 90,000 mm(3) or greater.
  • •Serum AST/ALT less then two times normal.
  • •ECOG performance status of 0 or 1 or
  • •Patients of both genders must be willing to practice effective birth control during this trial.
  • •No patients who are undergoing or have undergone in the past 3 weeks any other form of therapy except surgery for their cancer.
  • •No patients who have active systemic infections, coagulation disorders, autoimmune disease or other major medical illnesses of the cardiovascular or respiratory systems or any known immunodeficiency disease. Patients with cardiovascular disease will be eligible to receive peptide in IFA alone.
  • •No patients who require steroid therapy.
  • •No patients who are pregnant (because of possible side effects on the fetus).
  • •No patients who are known to be positive for hepatitis BsAG or HIV antibody (because of possible immune effects of these conditions).
  • •No patients who have any form of primary or secondary immunodeficiency. (The experimental treatment being evaluated in this protocol depends on an intact immune system. Patients who have decreased immune competence may be less responsive to the experimental treatment and more susceptible to its toxicities).

排除标准

  • 未提供

研究者

申办方类型
Nih

研究点 (1)

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