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ImCare Biotech recently published the results from its clinical study in the peer-reviewed journal Clinical and Translational Gastroenterology. The study, which was a prospective, double-blinded study, assessed Seravue’s ability to differentiate between patients with Hepatocellular Carcinoma (HCC), and benign liver conditions such as cirrhosis and chronic Hepatitis B and C. For any-stage HCC patients, Seravue demonstrated […]
(47612)(0)Pennsylvania June 8th, 2020: The FDA has granted Breakthrough Device Designation for Seravue® to support earlier diagnosis of Liver Cancer using a simple blood test. Seravue® is intended for use as an aid in the diagnosis of Hepatocellular Carcinoma (HCC), including early stage HCC, in patients with an elevated risk of developing HCC, in conjunction […]
(42354)(0)ImCare Biotech completes a prospective, blinded clinical study with over 500 patients in order to evaluate the use of their novel biomarker, Seravue®, for the purposes of detecting Hepatocellular Carcinoma in its early and later stages.
(36026)(0)August, 2019: ImCare Biotech is accepted into the CARE (Connecting Awardees with Regulatory Experts)ImCare Biotech is accepted into the CARE (Connecting Awardees with Regulatory Experts) program, which is being piloted by the NCI SBIR Development Center to encourage communications between promising small businesses and the FDA.
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