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The Sanderson Study: A Case Control Study for the Development of Multiomics Blood Tests for Cancer Screening

Completed
Conditions
Newly-diagnosed Cancers
Non-cancer Controls
Interventions
Diagnostic Test: Freenome Test
Registration Number
NCT05516927
Lead Sponsor
Freenome Holdings Inc.
Brief Summary

This protocol is a prospective, case-control multi-center diagnostic study to assess the sensitivity and specificity of blood-based screening tests for the early detection of multiple cancers.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
788
Inclusion Criteria
  • Age โ‰ฅ30 years within 30 days of enrollment
  • Able and willing to provide blood samples per protocol
  • Able to comprehend and willing to sign and date the informed consent and HIPAA
  • Authorization documents
  • Able and willing to allow existing health data to be utilized for study purposes

Key

Exclusion Criteria
  • Any history of solid organ or bone marrow transplantation
  • Any physical trauma or surgery requiring inpatient overnight hospitalization in the 30 days preceding enrollment
  • Received a blood transfusion in the 30 days preceding enrollment
  • A medical condition that, in the opinion of the Investigator, should preclude enrollment in the study
  • Known to be pregnant
  • Any therapy for cancer, including but not limited to surgery, chemotherapy, biologic therapy, immunotherapy, and/or radiation therapy in the 5 years preceding enrollment
  • Participated or currently participating in a clinical research study in which an experimental medication has been administered during the 30 days preceding enrollment
  • Participated or currently participating in another Freenome-sponsored clinical study
  • For non-cancer groups: Any previous cancer diagnosis in the 5 years preceding enrollment; OR recurrence of the same primary cancer within any timeframe; OR concurrent diagnosis of multiple primary cancers within any timeframe
  • For the cancer groups: Any previous cancer diagnosis in the 5 years preceding enrollment, apart from the current cancer diagnosis; OR recurrence of the same primary cancer within any timeframe; OR concurrent diagnosis of multiple primary cancers within any timeframe

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Non-cancer GroupFreenome Test* Collect Subject Data * Collect Blood Specimen
Cancer GroupFreenome Test* Collect Subject Data * Collect Blood Specimen
Primary Outcome Measures
NameTimeMethod
Comparison of Blood Samples from Cancer Case and Non-cancer Control Participants12 months

To compare blood samples from cancer case and non-cancer control subjects in order to develop and characterize blood-based multiomics tests in specific cancer types or in a combination of multiple cancers.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (23)

INOVA

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Fairfax, Virginia, United States

Crisp Regional Hospital

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Cordele, Georgia, United States

Advocate Lutheran General Hospital

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Park Ridge, Illinois, United States

Silver Cross Hospital and Medical centers

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Orland Park, Illinois, United States

Margaret Mary

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Batesville, Indiana, United States

Carroll County Memorial Hospital

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Carrollton, Missouri, United States

Hannibal Regional Hospital

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Hannibal, Missouri, United States

MUSC

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Charleston, South Carolina, United States

North Kansas City Hospital

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North Kansas City, Missouri, United States

St Joseph University

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Paterson, New Jersey, United States

Winona Health System

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Winona, Minnesota, United States

Renown Regional Medical Center

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Reno, Nevada, United States

University Health Truman Medical Center

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Kansas City, Missouri, United States

Cleveland Clinic

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Cleveland, Ohio, United States

Iredell Memorial Hospital

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Statesville, North Carolina, United States

Geisinger Bloomsburg Hospital

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Bloomsburg, Pennsylvania, United States

MacLeod Center for Cancer Treatment and Research

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Florence, South Carolina, United States

Elligo Health Research, Inc.

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Austin, Texas, United States

Allina Health Cancer Institute

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Minneapolis, Minnesota, United States

Henry Ford Health

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Detroit, Michigan, United States

Oregon Health and Science University

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Portland, Oregon, United States

Inspira Medical Center

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Mullica Hill, New Jersey, United States

Aurora St. Luke's Medical Center

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Milwaukee, Wisconsin, United States

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