SAN DIEGO, Aug. 24, 2011 /PRNewswire/ -- Biocept, Inc., a privately-held CLIA-certified laboratory testing company, focused on the detection and analysis of circulating tumor cells (CTCs) in cancer patients, and Clarient, Inc. (a GE Healthcare Company) today announced a collaboration on the commercialization of a proprietary blood test for CTCs in breast cancer patients, which includes the determination of HER2 status. Clarient and Biocept will market and sell Biocept's new OncoCEE-BR™ CTC test to community hospitals, pathologists and medical oncologists. Biocept will perform the test in its laboratories, and results will be interpreted by Clarient's highly respected pathology group (Clarient Pathology Services, Inc.). The test includes CTC enumeration and HER2 status of the detected CTCs by fluorescence in situ hybridization (FISH); it is the first commercially available CTC test to include analysis of a specific treatment-associated biomarker.
David Hale, Executive Chairman of Biocept, said, "We are very excited about this collaboration with Clarient, and feel there is real synergy between our two companies. We believe the combination of the technical advantages of the OncoCEE-BR™ test, and Clarient's highly regarded marketing and pathology capabilities, will enable the rapid education of the physician community about the benefits of CTC analysis for patients with breast cancer." He continued, "We think a blood-based, CTC-directed HER2 test, which can be performed when a treatment decision arises, has high potential, and expect that it will be used to support other laboratory and clinical information to provide physicians with the most current information on a tumor to help select the most appropriate course of therapy."
The OncoCEE-BR™ test includes enumeration of CTCs as well as the determination of HER2 status by FISH. Biocept intends to add ER/PR status determination to the test, an
|SOURCE Biocept, Inc.|
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