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COMPANY:
Datar Cancer Genetics

i
Other names: Datar Cancer Genetics | Datar PGx
Related tests:
Evidence

News

1year
Datar Cancer Genetics partners with Goodbody Health to offer innovative cancer screening (EIN News)
"Datar Cancer Genetics...announced its partnership with Goodbody Health Limited (Goodbody Health) to offer its innovative Circulating Tumor Cell (CTC) based multi-cancer screening solution Trucheck in the UK."
Licensing / partnership
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Trucheck™
over1year
US FDA Grants Breakthrough Designation for Blood Test to Help Diagnose Inaccessible Brain Tumors (PRNewswire)
"Datar Cancer Genetics Inc announced today that the US Food and Drug Administration (FDA) has granted 'Breakthrough Device Designation' for its 'TriNetra-Glio', a blood test to help in the diagnosis of brain tumors. This is the third test from the Company to have received the Breakthrough Device Designation from the US FDA. The Company's early-stage breast and prostate cancer detection tests became the first liquid biopsies to receive the Breakthrough Device Designation....A prospective, blinded study by a research team at the Imperial College, London, showed the test to be highly accurate. The test requires 15 ml blood and is indicated for patients where a brain biopsy, although necessary, cannot be performed or has been unsuccessful."
Breakthrough therapy designation • FDA event
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TriNetra™-Glio
almost2years
Artemis DNA to provide Datar Cancer Genetics liquid biopsy tests in the US, Vietnam under $250M deal (Genomeweb)
"Datar Cancer Genetics said...that it has struck a $250 million contract with US diagnostic laboratory company Artemis DNA, which will provide Datar's cancer detection liquid biopsies in the US and Vietnam...The five-year exclusive agreement covers two Datar cancer screening and diagnostic tests: Trucheck Pragma, a noninvasive, blood-based screening test for lung, stomach, colon, pancreas, prostate, breast, and ovarian cancers; and Cancertrack, which evaluates therapy response, resistance, and cancer recurrence in patients. The assays will be initially offered as laboratory-developed tests in the US, according to Datar."
Licensing / partnership
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Cancertrack™ • Trucheck™
2years
Artemis DNA, genetic and diagnostic testing company, expands services internationally to Vietnam (PRNewswire)
"Starting April 2022, Artemis DNA will begin offering its genetic testing technology and portfolio, as well as a new, revolutionary cancer screening called Trucheck™ Pragma through a partnership with Datar Cancer Genetics (Datar)...Under the partnership, Artemis DNA will be the exclusive distributor for Trucheck™ Pragma in Vietnam. Datar will support the successful rollout of the cancer screening solution, which has been proven through extensive clinical validations involving more than 40,000 participants."
Licensing / partnership
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Trucheck™
2years
Datar Cancer Genetics enters into partnership with The London Clinic to offer enhanced cancer testing services (EIN News)
"Datar Cancer Genetics has announced its partnership with The London Clinic...to provide precision oncology-based solutions to improve the detection and treatment of cancers. The partnership brings together two organisations that are dedicated to finding ever better ways to detect and treat cancers for the betterment of patients around the world."
Licensing / partnership
2years
FDA grants breakthrough designation for Datar Cancer Genetics early-stage prostate cancer detection blood test (PRNewswire)
"Datar Cancer Genetics today announced that the US Food and Drug Administration (FDA) has granted 'Breakthrough Device Designation' for its blood test to detect early-stage prostate cancer...The test has previously received CE certification and is already available in Europe as 'Trublood-Prostate'. The UK-NICE last year issued a MedTech Innovation Briefing that described the Test as a 'Game Changer'."
FDA event
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TruBlood®
over2years
FDA Grants Breakthrough Designation for Early-Stage Breast Cancer Detection Blood Test Developed by Datar Cancer Genetics (PRNewswire)
"Datar Cancer Genetics...announced that the US Food and Drug Administration (FDA) has granted 'Breakthrough Device Designation' for its 'TriNetra™' blood test to detect early-stage Breast Cancer...TriNetra™ uses a proprietary technology developed by the Company to detect Circulating Tumor Cells (CTCs) specific to Breast Cancer. Studies have shown that TriNetra™ can detect even Stage 0 (DCIS) and Stage 1 cancers with high accuracy. The test requires only 5 ml blood and is indicated for asymptomatic women above the age of 40 years with a physician's prescription."
Breakthrough therapy designation • FDA event
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TriNetra™