FDA Approves Freenome SimpleScreen CRC Blood Test for Abbott

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FDA Approves Freenome's SimpleScreen CRC Blood-Based Screening Test

Brisbane, Calif. and Abbott Park, Ill., USA - Freenome, Inc. (Nasdaq: FRNM) and Abbott (NYSE: ABT) have announced that the U.S. Food and Drug Administration (FDA) has granted approval for SimpleScreen CRC. This new blood-based screening test is designed for adults aged 45 and older who are at average risk for colorectal cancer (CRC). Abbott will exclusively commercialize the screening tool in the United States, offering a non-invasive option for the millions of Americans currently overdue for recommended screening.

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About Freenome Holdings, Inc.

Freenome is an early cancer detection company developing blood-based tests to detect cancer when it is most treatable. The company recognizes that no single technology can identify every cancer due to the disease’s inherent heterogeneity. Freenome’s approach combines a multiomics platform that analyzes multiple signals in the blood with artificial intelligence and machine learning to tune into cancer’s subtlest clues, even at the earliest stages of the disease.

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