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Abbott receives FDA Approval for hepatitis B assay

The assay is reportedly the first automated molecular test for assessing hepatitis B treatment
Written byJeffrey Bouley
| 3 min read

DES PLAINES, Ill.—The U.S. Food and Drug Administration (FDA) has given Abbott a big nod with its approval to the company to market its Abbott RealTime HBV assay for measuring viral load or the amount of hepatitis B virus (HBV) in a patient's blood.

"The Abbott RealTime HBV assay, which is the first and only automated HBV viral load test approved by the FDA, is an important tool for helping physicians make and adjust treatment decisions for newly diagnosed patients and those taking anti-viral medications," says Stafford O'Kelly, head of Abbott's molecular diagnostics business. "The test will also help improve laboratory productivity by automating the most labor intensive steps of HBV testing."

Shares of Abbott rose 99 cents to $50.33 in morning trading the day of the announcement, Sept. 1.

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