FDA Approves Agilent’s NSCLC Liquid Biopsy Companion Diagnostic Test
Agilent Technologies announced that the FDA has approved the ctDx FIRST as a companion diagnostic to identify advanced NSCLC.
Read MorePosted by Andy Lundin | Dec 14, 2022 | Lung Cancer |
Agilent Technologies announced that the FDA has approved the ctDx FIRST as a companion diagnostic to identify advanced NSCLC.
Read MorePosted by Andy Lundin | Nov 29, 2022 | Cancer |
As cancers grow and potentially spread to new parts of the body, they often shed cells and DNA into the blood stream.
Read MorePosted by Andy Lundin | Nov 24, 2022 | Melanoma |
Researchers found potential biomarkers that predict the likelihood for checkpoint inhibitor drugs to cause progression of melanoma cells.
Read MorePosted by Chris Wolski | Nov 22, 2022 | Unknown Origin & Other Cancer Types |
Positive liver cancer detection data demonstrates the promise of Delfi Diagnostics’ liquid biopsy platform in a new tumor type.
Read MorePosted by Andy Lundin | Nov 18, 2022 | Unknown Origin & Other Cancer Types |
A new AI blood testing tech called DELFI successfully detected more than 80% of liver cancer cases in a new study.
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