|

Tempus CRC Surveillance Study: A ctDNA Biomarker Profiling Study of Patients With CRC Using NGS Assays

RECRUITINGSponsored by Tempus AI
Actively Recruiting
SponsorTempus AI
Started2022-06-21
Est. completion2027-02
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations20 sites

Summary

The study is an observational multicenter evaluation of participants with colorectal cancer (CRC) who will receive longitudinal plasma ctDNA biomarker profiling in addition to their standard-of-care therapy and disease surveillance.

Eligibility

Age: 18 Years+Healthy volunteers accepted
Inclusion Criteria:

* Known or suspected colorectal adenocarcinoma (Stage I to IVA disease)
* Planning to undergo or has undergone a surgical resection for suspected adenocarcinoma of the colon or rectum with curative intent.
* 18 years old or older
* Willing and able to provide informed consent
* Willing to have additional blood samples collected during routine surveillance visits

Exclusion Criteria:

* Not willing to have additional blood samples collected
* Pathology that is not consistent with colorectal adenocarcinoma

Conditions2

CancerColorectal Cancer

Locations20 sites

Mercy Clinic Oncology - Fort Smith
Fort Smith, Arkansas, 72903
MemorialCare
Fountain Valley, California, 92708
Laura Macias562.706.2701LMacias@memorialcare.org
The Center for Cancer and Blood Disorders
Bethesda, Maryland, 20817
Kosunique Jenkins301-571-2016kosunique.jenkins@tempus.com
Mercy Clinic Oncology and Hematology - Joplin
Joplin, Missouri, 64804
Mercy Clinic Cancer and Hematology - Chub O'Reilly Cancer Center
Springfield, Missouri, 65804

Browse More Trials

Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.

This site does not provide medical advice. Always consult your doctor before considering enrollment in a clinical trial. Learn more on our About page.