Bristol-Myers Squibb's BARACLUDE Approved by the European Commission for the Treatment of Chronic Hepatitis B

Bristol-Myers Squibb BMY announced today that BARACLUDE (entecavir) has been approved by the European Commission on February 28th 2011 to treat chronic hepatitis B (CHB) in adult patients with evidence of decompensated liver disease. BARACLUDE(r) was already approved in Europe in June 2006 for use in adult patients with CHB with compensated liver disease and evidence of active viral replication, persistently elevated serum alanine aminotransferase (ALT) levels and histological evidence of active inflammation and/or fibrosis.