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ViroPharma Initiates Phase 2 Study of VP 20621 for Prevention of Recurrence of Clostridium difficile Infection (CDI)
Date:5/19/2011

ults of the Phase 2 study may not be predictive of how VP 20621 will perform in future studies. There can be no assurance that we will conduct additional studies with VP 20621 in the timeframes we expect or at all, or that VP 20621 can significantly reduce the incidence of recurrent disease for patients with CDI. The FDA or EMA may view the data regarding VP 20621 as insufficient or inconclusive, request additional data, require additional clinical studies, delay any decision past the time frames anticipated by us, limit any approved indications, or deny the approval of VP 20621. 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 2010, 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 The forward-looking statements contained in this press release may become outdated over time.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.  These forward-looking statements should not be relied upon as representing our assessments as of any date subsequent to the date of this press release.


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SOURCE ViroPharma Incorporated
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