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InterMune Reports Second Quarter 2014 Financial Results and Business Highlights
Date:8/6/2014

of November 23, 2014.  The FDA has granted pirfenidone Breakthrough Therapy Designation.  InterMune's research programs are focused on the discovery of targeted, small-molecule therapeutics and biomarkers to treat and monitor serious pulmonary and fibrotic diseases.
For additional information about InterMune and its R&D pipeline, please visit http://www.intermune.com/http://www.intermune.com/www.intermune.com.

Forward-Looking Statements This news release contains forward-looking statements within the meaning of section 21E of the Securities Exchange Act of 1934, as amended, that reflect InterMune's judgment and involve risks and uncertainties as of the date of this release, including without limitation: InterMune's expectations regarding the time period of the FDA's completion of its review of InterMune's NDA for pirfenidone, including the possibility of expedited development due to Breakthrough Therapy Designation; InterMune's expectations regarding the timing of commercial launch of pirfenidone in the U.S. and the timing and nature of its pre-launch preparations in the United States; InterMune's expectations regarding the potential for its pirfenidone analog compounds and expanding anti-fibrotic research and development pipeline; InterMune's expectations regarding the timing and results of its clinical trials, including LOTUSS and PANORAMA; InterMune's expectations regarding European regulatory, pricing and reimbursement developments; InterMune's expectations regarding the effects of seasonality and its planned European commercial launches on revenue; InterMune's expectations with respect to Canada of securing coverage from private insurance plans and reimbursement from public (provincial) drug reimbursement plans including the timing thereof; and InterMune's projected revenue from sales of Esbriet and operating expenses f
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SOURCE InterMune, Inc.
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