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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
View on ClinicalTrials.gov →
NCT05234177
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
The Center for Cancer and Blood Disorders
Bethesda, Maryland, 20817
Mercy Clinic Oncology and Hematology - Joplin
Joplin, Missouri, 64804
Cynthia MeyerCynthia.Meyer@mercy.net
Mercy Clinic Cancer and Hematology - Chub O'Reilly Cancer Center
Springfield, Missouri, 65804
Jennifer HyltonJennifer.Hylton@mercy.net
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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.
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Actively Recruiting
SponsorTempus AI
Started2022-06-21
Est. completion2027-02
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations20 sites
View on ClinicalTrials.gov →
NCT05234177