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临床试验/JPRN-jRCT2080222348
JPRN-jRCT2080222348未知3 期

A phase 3, randomized, open-label, multi-center clinical study to observe the efficacy and safety of TMX-67 compared to allopurinol in patients with a malignant tumor receiving chemotherapy

TEIJIN PHARMA LIMITED0 个研究点目标入组 100 人开始时间: 2013年12月26日最近更新:
适应症

试验速览

阶段
3 期
入组人数
100

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

入选标准

  • Patients with intermediate or high risk of tumor lysis syndrome (TLS)

排除标准

  • 1)Patients with diagnosis of Laboratory TLS (LTLS) or Clinical TLS (CTLS).
  • 2)Patients with severe hepatic insufficiency.
  • 3)Patients with severe renal insufficiency.
  • 4)Performance status of 3 to 4.

研究者

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