跳至主要内容
临床试验/EUCTR2020-006057-21-PL
EUCTR2020-006057-21-PL进行中(未招募)1 期

A phase 3b, multi-center, open-label, treatment optimization study of oral asciminib in patients with Chronic Myelogenous Leukemia in chronic phase (CML-CP) previously treated with 2 or more tyrosine kinase inhibitors

ovartis Pharma AG0 个研究点目标入组 186 人开始时间: 2021年12月9日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
186

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Male or female patients with a diagnosis of CML-CP = 18 years of age
  • Treatment with a minimum of 2 or more prior TKIs (i.e. imatinib, nilotinib, dasatinib, bosutinib, radotinib or ponatinib)
  • Warning or failure (adapted from the 2020 ELN Recommendations) or intolerance to the most recent TKI therapy at the time of screening
  • Adequate end organ function (as per central laboratory tests)
  • Other protocol defined inclusion criteria may apply.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 124
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 62

排除标准

  • Known presence of the BCR-ABL1 T315I mutation at any time prior to study entry
  • Known history of AP/BC
  • Previous treatment with a hematopoietic stem-cell transplantation
  • Patient planning to undergo allogeneic hematopoietic stem cell transplantation
  • Uncontrolled cardiac repolarization abnormality
  • Severe and/or uncontrolled concurrent medical disease that in the opinion of the investigator could cause unacceptable safety risks or compromise compliance with the protocol
  • History of acute pancreatitis within 1 year of study entry or past medical history of chronic pancreatitis
  • History of ongoing active acute or chronic liver disease
  • Other protocol defined exclusion criteria may apply

研究者

相似试验