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Idenix Announces Data Presentations at the 2007 Digestive Disease,Week Meeting

a poster session beginning on Sunday, May 20, 2007 at 8:00 a.m. EDT.

Dr. David Standring, Senior Vice President, Biology at Idenix Pharmaceuticals, will present "Resistance Determination in Patients Experiencing Virologic Breakthrough Following Telbivudine or Lamivudine Therapy in the International GLOBE Trial" in a poster session beginning on Sunday, May 20, 2007 at 8:00 a.m. EDT.

Important Information About TYZEKA(R) (telbivudine)

TYZEKA is indicated for the treatment of chronic hepatitis B in adult patients with evidence of viral replication and either evidence of persistent elevations in serum aminotransferases (ALT or AST) or histologically active disease. This indication is based on virologic, serologic, biochemical and histologic responses after one year of treatment in nucleoside-treatment-naive adult patients with HBeAg-positive and HbeAg-negative chronic hepatitis B with compensated liver disease. For full prescribing information please visit http://www.tyzeka.com .

    Important Safety Information about TYZEKA (telbivudine)


    -- Lactic acidosis and severe hepatomegaly with steatosis, including fatal

       cases, have been reported with the use of nucleoside analogues alone or

       in combination with antiretrovirals. Severe acute exacerbations of

       hepatitis B have been reported in patients who have discontinued anti-

       hepatitis B therapy, including TYZEKA. Hepatic function should be

       monitored closely with both clinical and laboratory follow-up for at

       least several months in patients who discontinue anti-hepatitis B

       therapy. If appropriate, resumption of antihepatitis B therapy may be

       warranted.

    -- Cases of myopathy have been reported with TYZEKA use several weeks to

       months after starting therapy. Myopathy has also been reported with

       some other drugs in this class. Physicians considering concomitan
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