This in vitro diagnostic (IVD) assay, which has been cleared by the U.S. Food and Drug Administration (FDA), supports physicians in delivering guideline-based care for patients with solid tumors. Its ability to simultaneously analyze multiple biomarkers, even with limited tissue samples, enables insights that can support patient care and clinical management. For many, this could mean the difference between starting an effective patient management plan sooner or facing delays that could impact their prognosis. With this CE-marking, the test can now be offered by more laboratories across the EU, expanding patient access to personalized cancer care.

“This accomplishment reflects Labcorp’s commitment to advancing precision medicine and improving patient care,” said Shakti Ramkissoon, M.D., Ph.D., MBA, vice president, medical lead for oncology at Labcorp. “With both FDA clearance and IVDR CE-mark, this test sets a new standard for quality and performance in cancer diagnostics. Importantly, it also provides our biopharma partners with a reliable, regulatory-ready solution to de-risk multiyear clinical trial strategies, ensuring continuity in NGS testing for trials that will extend beyond the IVDR transition timelines.”