跳至主要内容
临床试验/JPRN-jRCT2080221134
JPRN-jRCT2080221134未知1 期

A phase I and pharmacokinetic study to determine the safety of ET-743 administered as a continuous intravenous infusion over 24 hours every 21 days in patients with soft tissue sarcoma.

Taiho Pharmaceutical Co., Ltd.0 个研究点开始时间: 2010年6月22日最近更新:
适应症

试验速览

阶段
1 期

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 18age old 至 ot applicable(—)
性别
All

入选标准

  • 1)Patients who have a histologically confirmed soft tissue sarcoma.
  • 2)Patients who have failed the standard therapy.

排除标准

  • 1)Serious concomitant illness.
  • 2)Prior therapy-related toxicity.

研究者

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