Genetic Cancer Test Granted FDA Breakthrough Device Designation
The designation’s accelerated regulatory review is intended to expedite use of the diagnostic in pharmaceutical trials.
Read MorePosted by Chaunie Brusie | Jun 30, 2019 | Breast, Lung Cancer |
The designation’s accelerated regulatory review is intended to expedite use of the diagnostic in pharmaceutical trials.
Read MorePosted by Chaunie Brusie | May 13, 2019 | Culture Media |
LabCorp joins Qiagen ‘Day-One’ lab readiness program designed to deliver precision medicine to patients faster.
Read MorePosted by Chaunie Brusie | Apr 30, 2019 |
Patient-specific assays detect low-volume minimal residual disease at high levels of sensitivity and characterize the landscape of relapsing lung cancer.
Read MorePosted by Chaunie Brusie | Apr 30, 2019 | Lung Cancer |
The draft LCD applies to advanced cancer patients who are covered by Medicare for next-generation sequencing of tumor tissue, but have insufficient or unavailable tissue samples.
Read MorePosted by Chaunie Brusie | Apr 18, 2019 | Lung Cancer |
The tests will use patient breath samples to identify individual biomarkers that can predict a spectrum of diseases.
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