Zeffix Approved For Chronic Hepatitis B Treatment In The E.U.
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Zeffix Approved For Chronic Hepatitis B Treatment In The E.U.

LAVAL, QC -- Aug. 2, 1999 -- The European Commission has approved BioChem Pharma Inc.’s Zeffix (lamivudine), an oral treatment for chronic hepatitis B, in all 15 countries of the European Union for the treatment of adult patients with chronic hepatitis B and evidence of viral replication.

In addition to significantly reducing liver inflammation, it has been shown in clinical trials to produce, after three years of continued treatment, seroconversion rates of 65 percent in patients with active liver disease and 40 percent in the overall patient group.

According to World Health Organization data, approximately 350 million people around the world are long-term (chronic) carriers of the hepatitis B virus (HBV), including an estimated four million people in the European Union.

Zeffix is already available in a number of countries including the United States (as Epivir-HBV), Canada (as Heptovir) and South Korea, and has been approved and is awaiting launch in others such as China.

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