ClinicalTrials.Veeva

Menu

TEMPUS ARIES: A Biobank Registry Platform Study in Oncology

Tempus AI logo

Tempus AI

Status

Enrolling

Conditions

Cancer

Study type

Observational

Funder types

Industry

Identifiers

NCT06207032
Pro00076336 (Other Identifier)
TP-CA-007

Details and patient eligibility

About

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.

Enrollment

500 estimated patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. ≥18 years of age
  2. Willing to participate in the research
  3. Able to provide informed consent
  4. Must be diagnosed with cancer

Exclusion criteria

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

Trial design

500 participants in 6 patient groups

Cohort 001: KRAS mutated CRC
Description:
No intervention.
Cohort 002: KRAS mutated PDAC
Description:
No intervention.
Cohort 003: KRAS mutated NSCLC
Description:
No intervention.
Cohort 004: Gastric 1L Plus
Description:
No intervention.
Cohort 005: mCRPC 1L Plus
Description:
No intervention.
Cohort 006: Pan Tumor ADCs
Description:
No intervention.

Trial contacts and locations

26

Loading...

Central trial contact

Lauren Lopez

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems