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Intercept Pharmaceuticals Announces Positive Phase II Results for INT-747 as a Treatment for Primary Biliary Cirrhosis
Date:10/27/2009

ad drug candidate, the FXR agonist INT-747, is currently being advanced for chronic liver disease indications and the company has been granted orphan status in the US for the PBC indication. The company's next candidate in the pipeline, INT-777, is a selective TGR5 agonist being advanced to an IND, projected for the second quarter of 2010.

For more information about Intercept, please go to www.interceptpharma.com, and for information about Intercept's lead investor, Genextra S.p.A., please go to www.genextra.it.

SOURCE Intercept Pharmaceuticals, Inc.


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SOURCE Intercept Pharmaceuticals, Inc.
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