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ViroPharma Announces Presentation of Cinryze(TM) Data in Acute Treatment of Hereditary Angioedema
Date:11/12/2008

of the results of any future testing. The FDA may view the data regarding the use of Cinryze for acute treatment of HAE we intend to submit as a supplemental BLA as insufficient or inconclusive, request additional data, delay any decision past the time frames anticipated by us, limit any approved indications, or deny the approval of Cinryze for acute treatment of HAE. These factors, and other factors, including, but not limited to those described in ViroPharma's annual report on Form 10-K and quarterly reports on Form 10-Q filed with the Securities and Exchange Commission during 2008, could cause future results to differ materially from the expectations expressed in this press release. The forward-looking statements contained in this press release may become outdated over time. ViroPharma does not assume any responsibility for updating any forward-looking statements.


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SOURCE ViroPharma Incorporated
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