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Schering-Plough Reports Top-Line Results of the IDEAL Study
Date:1/14/2008

Please see the Pegasys and Copegus product inserts for information on

these products.

2 SVR, the protocol specified primary efficacy endpoint, is defined as

achievement of undetectable HCV-RNA at 24 weeks after the end of

treatment. Per protocol, if a patient did not have a 24-week post-

treatment assessment, the patient's 12-week post-treatment assessment

was utilized.

3 Roche Cobas Taqman 1.0 assay; lower limit of detection is 15 IU/mL.


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SOURCE Schering-Plough Corporation
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