跳至主要内容
临床试验/jRCT2080221095
jRCT2080221095未知1 期

A Phase I, Open-Label Study to Assess the Safety, Tolerability and Pharmacokinetics of Ascending Doses of MEDI-575 in Patients With Advanced Solid Malignancies

AstraZeneca0 个研究点开始时间: 待定

试验速览

阶段
1 期
发起方
AstraZeneca

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
干预模型
Allocation: Non-Randomized Endpoint Classification: Safety Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment

入排标准

年龄范围
20age old over 至 No limit(—)
性别
All

入选标准

  • Having advanced solid malignancy for which no curative or standard therapies exist
  • Karnofsky performance status of 60 or more
  • Patients must have histological confirmed diagnosis of HCC with no standard therapy available (for only expansion part)

排除标准

  • Inadequate bone marrow reserve or organ function
  • Major surgery within 4 weeks or minor surgery within 2 weeks prior to receipt of MEDI-
  • Patients must have no unhealed wounds or unhealed fractures
  • History of allergy or reaction to any component of the MEDI-575 and/or monoclonal antibody

研究者

发起方
AstraZeneca

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