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 Andy Lundin | Aug 9, 2023 | Lung Cancer |
Millions of Americans with tobacco-related lung disease have symptoms that do not fit any existing tobacco-related disease criteria.
Read MorePosted by Andy Lundin | Aug 8, 2023 | Unknown Origin & Other Cancer Types |
Blood disorders known as MDS are difficult to diagnose putting patients at increased risk for treatment mistakes from misdiagnosis.
Read MorePosted by Andy Lundin | Jul 28, 2023 | Cancer |
A team of scientists developed a label-free SERS-Artificial intelligence method for cancer screening (SERS-AICS).
Read MorePosted by Andy Lundin | Jul 27, 2023 | Cancer |
New blood testing tech combines genome-wide sequencing of single molecules of DNA shed from tumors and machine learning.
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