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InterMune Announces Progress on Pirfenidone in IPF
Date:4/21/2008

to failure to achieve the clinical trial results required to commercialize our product candidates; (iii) risks related to timely patient enrollment and retention in clinical trials; and (iv) risks that the results of the InterMune CAPACITY trials of pirfenidone may differ materially from those of the Shionogi & Co., Ltd. Phase 3 trial of pirfenidone. The risks and other factors discussed above should be considered only in connection with the fully discussed risks and other factors discussed in detail in the Form 10-K and InterMune's other periodic reports filed with the SEC, all of which are available via InterMune's web site at http://www.intermune.com.


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SOURCE InterMune, Inc.
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