500 Participants Needed

Biomarker Profiling for Cancer

Recruiting at 27 trial locations
LL
Overseen ByLauren Lopez
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: Tempus AI
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to study cancer patients by analyzing their blood over time to identify specific DNA markers. Researchers seek to understand how these markers change and their implications for cancer treatment. The trial does not test a new drug; instead, it focuses on gaining a deeper understanding of the disease. Patients with cancer who are willing to provide additional blood samples during regular treatment may be suitable for this study. As an unphased study, this trial offers participants the chance to contribute to groundbreaking research that could enhance cancer understanding and treatment for future patients.

Why are researchers excited about this trial?

Researchers are excited about the TEMPUS ARIES biobank registry platform because it offers a new way to gather and analyze large-scale genomic and clinical data in oncology. Unlike traditional studies that focus on a single treatment or drug, this platform aims to create a comprehensive database that can accelerate the understanding of cancer biology and the development of personalized treatments. By enabling real-time data sharing among researchers, TEMPUS ARIES could lead to more effective and tailored treatment plans, potentially improving patient outcomes faster than current methods.

Who Is on the Research Team?

MT

Michelle Ting-Lin, MD

Principal Investigator

Tempus AI, Inc.

Are You a Good Fit for This Trial?

Inclusion Criteria

You are able to understand and agree to participate in the study.
You must have been told by a doctor that you have cancer.
You are happy to take part in the study.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Biomarker Profiling

Participants undergo longitudinal plasma ctDNA biomarker profiling at specific time points in addition to standard of care therapy

5 years

Follow-up

Participants are monitored for safety and effectiveness after biomarker profiling

5 years

What Are the Treatments Tested in This Trial?

Find a Clinic Near You

Who Is Running the Clinical Trial?

Tempus AI

Lead Sponsor

Trials
18
Recruited
20,700+
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