跳至主要内容
临床试验/NCT06600568
NCT06600568招募中不适用

Identification of Targetable Vulnerabilities in Redox Homeostasis Pathways as a Novel Therapeutic Approach for Human T-cell Malignancies

Istituto Oncologico Veneto IRCCS3 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2025年3月18日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
120
试验地点
3
主要终点
Primary outcome

研究概览

简要总结

This multicenter translational study, with prospective and retrospective samples, aims to identify new strategies to selectively eliminate neoplastic T cells by modulating intracellular ROS levels.

Interactions between drugs capable of activating the apoptotic process (e.g., Venetoclax) and drugs capable of altering ROS homeostasis (e.g., inhibitors of the enzyme glucose-6-phosphate dehydrogenase) will be examined.

The most promising compounds will be selected based on results obtained in vitro on cell lines and PDX already available in the laboratory, and then will be assayed ex vivo in cells obtained from patients with resistant/refractory T-cell neoplasms.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Other

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with pre- and post-thymic T-cell leukemia/lymphoma
  • Patients of both sexes
  • Age of patients older than 18 years
  • Patient is willing to provide written and signed informed consent for participation in the study

排除标准

  • Serious illness or medical condition that does not allow the patient to be managed according to standard treatment protocols, including uncontrolled active infection.

结局指标

主要结局

Primary outcome

时间窗: Through study completion, an average of 2 years

Response of leukemic cells to treatments that remodulate redox state and apoptosis from a molecular point of view, ex vivo,through the development of a multidimensional approach aimed at reducing the chemoresistance of T neoplasms

次要结局

  • Secondary outcome(Through study completion, an average of 2 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (3)

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