The Duet System is intended for
in-vitro diagnostic use as an aid to the pathologist in thedetection, classification and counting of cells of interest based on color,intensity, size, pattern and shape. Duet has
U.S. Food and Drug Administration(FDA) clearances for the automated imaging and analysis of certainhematopoietic cells, amniotic cells, cells in urine specimens and FFPE breasttissue specimens.
BioView is engaged in clinical trials that will supportfuture global regulatory submissions for the use of the company's automatedscanning microscope and image analysis system with Abbott's Vysis ALK FISHtest. The imaging system is designed to scan specimen slides after FISHanalysis and enable automated enumeration to assist in determining fluorescentsignal counts in lung tissue samples. This can aid the pathologist indetecting, classifying and counting cells examined with the ALK FISH test onany computer screen and/or fluorescent microscope. The scans can be convertedinto electronic files for permanent medical records and allow consultationswith other physicians locally or remotely. In addition, Abbott plans to conductclinical studies to develop a version of the Vysis ALK FISH kit for use withits VP2000 Processor to automate the sample pretreatment steps.
Abbott's Vysis ALK FISH Probe test is FDA-approved and isalso available in South Korea, Japan, Israel, Canada and Europe as a companiondiagnostic, to detect rearrangements of the 2p23 chromosome of the ALK gene inNSCLC patients. The test is performed on lung tissue specimens with aready-to-use kit that includes positive ALK control slides and a probe that ispremixed with a buffer optimized for use in the formalin-fixed, paraffinembedded protocol.