FDA Approves VENTANA PD-L1 as a CDx for NSCLC Subtype
The FDA approved the VENTANA PD-L1 (SP263) Assay as a CDx to identify NSCLC patients eligible for treatment with Libtayo (cemiplimab).
Read MorePosted by Andy Lundin | Mar 9, 2023 | Lung Cancer |
The FDA approved the VENTANA PD-L1 (SP263) Assay as a CDx to identify NSCLC patients eligible for treatment with Libtayo (cemiplimab).
Read MorePosted by Andy Lundin | Mar 9, 2023 | Leukemia |
Research shows benefits of screening patients in remission from acute myeloid leukemia for residual disease prior to a bone marrow transplant.
Read MorePosted by Andy Lundin | Mar 3, 2023 | Urine Analyzers |
Researchers developed a urine sensor that can amplify the light signal of metabolites in urine and in diagnosing cancer in the field.
Read MorePosted by Andy Lundin | Mar 3, 2023 | Lab Automation, Molecular Diagnostics |
Automated NGS platforms can help determine if a patient is fit for a targeted therapy, enabling more effective precision medicine.
Read MorePosted by Chris Wolski | Mar 2, 2023 | Prostate, Unknown Origin & Other Cancer Types |
Veracyte CEO Marc Stapley outlines how single-cancer testing is giving pathologists, clinicians, and patients an edge.
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