跳至主要内容
临床试验/NCT07468656
NCT07468656尚未招募不适用

Analysis of Blood Samples in Small Cell Lung Cancer Patients Treated With Tarlatamab

Duke University0 个研究点目标入组 25 人开始时间: 2026年10月1日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
25
主要终点
Number of blood samples collected to better characterize tarlatamab in real-world setting

研究概览

简要总结

The overall objective of this project is to prospectively collect blood samples throughout treatment with tarlatamab in patients with small cell lung cancer (SCLC). These samples will then be analyzed through a variety of assays to better characterize tarlatamab in the real-world setting.

The investigators will prospectively collect blood samples from 25 patients on days 1, 8, and 15 of tarlatamab treatment, as well as after each interval scan for disease monitoring. The investigators will also collect patient data including demographics and baseline characteristics, primary diagnosis, treatment history, and disease monitoring and progression.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

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

  • Pathologically documented small cell lung cancer (SCLC) or neuroendocrine tumor
  • Appropriate candidate for treatment with tarlatamab based on investigator discretion
  • Age > 18 years
  • Signed written informed consent including HIPAA according to institutional guidelines

排除标准

  • Does not meet all inclusion criteria

结局指标

主要结局

Number of blood samples collected to better characterize tarlatamab in real-world setting

时间窗: Days 1, 8, and 15 of tarlatamab and after each interval scan for disease assessment

Studies to better understand tarlatamab may include, but are not limited to, the following: 1) predictors of response to treatment with tarlatamab, 2) identification of predictive biomarkers for the development of cytokine release syndrome (CRS) and/or immune effector cell-associated neurotoxicity syndrome (ICANS), 3) characterization of the immune cell environment induced by tarlatamab, 4) identification of resistance mechanisms to tarlatamab treatment, and 5) development of potential translational correlates.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

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