Healthcare Industry News:  Oncomine Dx Target Test 

Diagnostics Oncology Regulatory

 News Release - October 17, 2018

Thermo Fisher Scientific CE Marks Oncomine Dx Target Test

CE IVD Mark brings NGS-based clinical test for solid tumors to Europe

CARLSBAD, Calif., Oct. 17, 2018 -- (Healthcare Sales & Marketing Network) -- Marking a milestone in bringing its Oncomine Dx Target Test to Europe, Thermo Fisher Scientific today announced that it has CE-IVD marked its next-generation sequencing (NGS)-based solution that screens biomarkers across solid tumors. Thermo Fisher will highlight the test during the European Society for Medical Oncology (ESMO) Congress (booth #203) being held in Munich, Germany from Oct. 19–23.

Oncomine Dx Target Test is CE marked as an in vitro diagnostic for detection of 46 cancer-driver gene variants. All biomarkers on the panel are associated with approved and investigative targeted therapies in solid tumors, including EGFR, BRAF, KRAS and ERBB2 mutations, as well as ALK, ROS1, RET, NTRK and MET fusions. It is also validated as a companion diagnostic (CDx) for approved therapies in non-small cell lung cancer (NSCLC), including ALK, ROS1 and BRAF kinase inhibitors, as well as EGFR exon 19 deletions and L858R tyrosine kinase inhibitors.

"Having access to the Oncomine Dx Target Test will improve our ability to care for cancer patients by allowing us to have multiple therapeutic targets in one test requiring very little tissue," said Fernando López-Ríos, director of the targeted therapies laboratory at the Hospital Universitario HM Sanchinarro in Madrid, Spain. "Reducing the number of tests needed to match patients with the right targeted therapy is a major advancement for precision medicine in Europe."

Oncomine Dx Target Test, which received approval by the U.S. Food and Drug Administration (FDA) as a CDx for NSCLC in 2017, is designed to return results with as little as 10 nanograms of nucleic acid. This is a critical advantage that helps reduce the risk of sample depletion and the need for additional invasive biopsies. While the single biomarker testing approach can take weeks to match patients with the right treatment, data from Oncomine Dx Target Test can be obtained in as little as four days to help expedite tumor profiling and therapy selection.

"Obtaining the CE-IVD Mark represents a significant step in our endeavor to democratize NGS testing and precision oncology across the globe," said Joydeep Goswami, president of clinical next generation sequencing at Thermo Fisher. "We are encouraged by the number of national reference laboratories that are now providing Oncomine Dx Target Test to oncologists. This indicates a shift from the single biomarker testing approach to a more efficient testing regime that saves precious time for their cancer patients."

About Thermo Fisher Scientific

Thermo Fisher Scientific Inc. is the world leader in serving science, with revenues of more than $20 billion and approximately 70,000 employees globally. Our mission is to enable our customers to make the world healthier, cleaner and safer. We help our customers accelerate life sciences research, solve complex analytical challenges, improve patient diagnostics, deliver medicines to market and increase laboratory productivity. Through our premier brands – Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific and Unity Lab Services – we offer an unmatched combination of innovative technologies, purchasing convenience and comprehensive services. For more information, please visit

Source: Thermo Fisher Scientific

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