Tempus’ Solid Tumor CDx Test Gets Breakthrough Device Designation
The U.S. FDA has granted Tempus Breakthrough Device Designation for its HLA-LOH assay as a companion diagnostic (CDx) test for solid tumors.
Read MorePosted by Andy Lundin | Aug 17, 2023 | Cancer |
The U.S. FDA has granted Tempus Breakthrough Device Designation for its HLA-LOH assay as a companion diagnostic (CDx) test for solid tumors.
Read MorePosted by Melanie Hamilton-Basich | Jun 15, 2023 | Cancer |
Culmination Bio and Cofactor Genomics are partnering to leverage biobank samples and data to develop the OncoPrism test for 11 cancers.
Read MorePosted by Melanie Hamilton-Basich | Jun 7, 2023 | Cancer |
The analysis showed strong performance of Grail’s MCED methylation-based platform in the symptomatic population of more than 6,000 patients
Read MorePosted by Chris Wolski | Jun 1, 2023 | Cancer |
Labcorp has launched Labcorp Plasma Focus, a new liquid biopsy test enabling targeted therapy selection for solid tumors.
Read MorePosted by Melanie Hamilton-Basich | Apr 28, 2023 | Uncategorized |
Generalist medical AI models can integrate multiple data types — such as MRI scans, X-rays, blood test results, medical texts, and genomic testing — to perform a range of tasks
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