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临床试验/JPRN-jRCT2080224127
JPRN-jRCT2080224127已完成1 期

A Study to Evaluate CTX-712 in Advanced, Relapsed or Refractory Malignant Cancer Patients

Chordia Therapeutics Inc.0 个研究点目标入组 79 人开始时间: 2018年10月30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
79

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

  • 1) Subjects must have an advanced, relapsed or refractory cancer
  • - For a cohort of hematological cancers,subjects must have an MDS, CMML or AML (excluding APL) according to World Health Organization (WHO) criteria.
  • - As for MDS, subjects must be considered an intermediate, high, or very high risk according to the Revised International Prognostic Scoring System (IPSS-R)
  • 2) Subjects must relapse or refractory to standard therapies, or not eligible for standard therapies.
  • 3) Subjects must be an eastern cooperative oncology group (ECOG) performance status of 0 or 1
  • 4) Subjects must have more than 90 days life expectancy
  • 5) Subjects must have adequate major organ functions

排除标准

  • 1) Patients with uncontrolled complications
  • 2) Patients with active multiple primary cancers that require specific treatments
  • 3) In a cohort of hematologic cancer patients, those who have received allogenic hematopoietic stem cell transplantation
  • 4) Patients having a medical history of congenital retinal degenerative disease,optic nerve or retinal diseases

研究者

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