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See today's BioWorld MedTech
Home » FDA greenlights Biovica cancer biomarker assay
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FDA greenlights Biovica cancer biomarker assay

Aug. 1, 2022
By Catherine Longworth
The U.S. FDA has granted 510(k) clearance to a blood-based biomarker assay for disease monitoring of patients with metastatic breast cancer (MBC). The Divitum Tka assay, developed by Uppsala, Sweden-based Biovica International AB, measures the activity of the enzyme thymidine kinase-1 (TK1) which is highly associated with cell proliferation and a predictive marker of tumor aggressiveness. It is the first liquid cancer cell proliferation biomarker assay to be approved by the FDA for use in monitoring metastatic breast cancer.
BioWorld MedTech Cancer U.S.

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