Colon Cancer

Abbott Receives FDA Approval for First Automated Molecular Test for Assessing Hepatitis B Treatment

Published in Hepatitis Weekly, September 13th, 2010

Des Plaines, Illinois - Abbott (NYSE: ABT) announced it has received approval from the U.S. Food and Drug Administration (FDA) to market the Abbott RealTime HBV assay for measuring viral load or the amount of hepatitis B virus (HBV) in a patient's blood. It is the first and only approved test capable of automating HBV viral load testing from sample extraction to final results.

The Abbott RealTime HBV assay, based on real-time PCR (polymerase chain reaction) technology, is now available for laboratories that use the Abbott m2000 automated instrument system for molecular diagnostic testing. The test offers sensitive measurement (quantitation) of HBV in human plasma or...

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Source: Hepatitis Weekly (2010-09-13)

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