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FDA Advisory Committee Recommends Approval of InterMune's Esbriet(R) (pirfenidone) for Idiopathic Pulmonary Fibrosis
Date:3/9/2010

o the European Medicines Agency (EMA), seeking approval to market Esbriet for the treatment of IPF patients in the European Union.  Esbriet (pirfenidone) has been granted Orphan Drug status in Europe.

Conference Call and Webcast Details

InterMune will host a conference call today at 5:00 p.m. EST to discuss Esbriet.  Interested investors and others may participate in the conference call by dialing 888-799-0528 (U.S.) or 973-200-3372 (international), conference ID# 61659499.  A replay of the webcast and teleconference will be available approximately three hours after the call.

To access the webcast, please log on to the company's website at www.intermune.com at least 15 minutes prior to the start of the call to ensure adequate time for any software downloads that may be required.

The teleconference replay will be available for 10 business d
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SOURCE InterMune, Inc.
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