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临床试验/JPRN-jRCT2080222290
JPRN-jRCT2080222290已完成1 期

A phase 1 clinical study of WT2725 in patients with advanced solid malignancies.

Sumitomo Dainippon Pharma Co., Ltd.0 个研究点目标入组 8 人开始时间: 2013年11月14日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
8

研究概览

简要总结

This study was conducted to assess the safety of WT2725 in patients with advanced solid tumors, to determine MTDs, and to exploratory evaluate efficacy and biomarkers. No DLT was observed in any of the cohorts, and due to a change in the development plan, three additional patients were added to Cohort 2, and the MTD could not be determined because they were not evaluated in six patients.

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 ot applicable(—)
性别
All

入选标准

  • out-patient
  • Main Inclusion criteria
  • - Patients >= 20 year old at informed consent
  • - ECOG performance status: 0 or 1
  • - Histologically or cytologically diagnosed as solid tumor
  • - Refractory to standard treatment or no standard treatment is established

排除标准

  • Main Exclusion criteria
  • - Positive for HIV and HCV antibody, HBV surface antigen within 90 days prior to enrollment
  • - Symptomatic brain metastasis
  • - Previous treatment with WT2725 or WT1 peptide

研究者

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