跳至主要内容
临床试验/NCT06207032
NCT06207032招募中不适用

TEMPUS ARIES: A Biobank Registry Platform Study in Oncology

Tempus AI32 个研究点 分布在 2 个国家目标入组 500 人开始时间: 2024年6月26日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
Tempus AI
入组人数
500
试验地点
32
主要终点
Changes in ctDNA from baseline, on-treatment and post-treatment blood samples.

研究概览

简要总结

This study is a non-interventional, multicenter, multicohort evaluation of participants with cancer who will undergo longitudinal plasma ctDNA biomarker profiling at specific time points in addition to standard of care therapy.

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 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • ≥18 years of age
  • Willing to participate in the research
  • Able to provide informed consent
  • Must be diagnosed with cancer

排除标准

  • 1. Not willing or able to have additional blood samples collected

研究组 & 干预措施

Cohort 001: KRAS mutated CRC

No intervention.

Cohort 002: KRAS mutated PDAC

No intervention.

Cohort 003: KRAS mutated NSCLC

No intervention.

Cohort 004: Gastric 1L Plus

No intervention.

Cohort 005: mCRPC 1L Plus

No intervention.

Cohort 006: Pan Tumor ADCs

No intervention.

Cohort 007: Stage III-IV EGFR Activating Mutation NSCLC

No intervention.

结局指标

主要结局

Changes in ctDNA from baseline, on-treatment and post-treatment blood samples.

时间窗: 5 years

Assess ctDNA kinetics using ctDNA clearance factors such as time to clearance, best overall clearance rate, best confirmed clearance, and time to ctDNA recurrence and correlate with standard of care therapy real-world outcomes such as overall survival, progression-free survival, time to next treatment, and time to treatment discontinuation.

次要结局

  • Generation of DNA, RNA, immune and other multiomic datasets.(5 years)

研究者

发起方
Tempus AI
申办方类型
Industry
责任方
Sponsor

研究点 (32)

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