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statistical significance of our clinical trials;
-- our ability to successfully complete our clinical trials of VIA-2291 on
expected timetables and the outcomes of such clinical trials;
-- complexities in designing and implementing cardiovascular clinical
trials using histological examinations, measurement of biomarkers,
medical imaging and atherosclerotic plaque bioassays;
-- the results of our clinical trials, including without limitation, with
respect to the safety and efficacy of VIA-2291;
-- our ability to achieve clinical trial endpoints;
-- if the results of the ACS and CEA studies, upon further review and
are revised, interpreted differently by regulatory authorities or
negated by later stage clinical trials;
-- our ability to properly design and conduct additional clinical trials;
-- the outcome of any legal proceedings;
-- our ability to obtain necessary FDA approvals;
-- our ability to successfully commercialize VIA-2291;
-- our ability to obtain and protect our intellectual property related to
our product candidates;
-- our potential for future growth and the development of our product
pipeline;
-- our ability to form and maintain collaborative relationships to
develop and commercialize our product candidates;
-- general economic and business conditions; and
-- the other risks described under Item IA "Risk Factors" in our Annual
Report on Form 10-K for the fiscal year ended December 31, 2007 on
file with the SEC.
All forward-looking statements attributable to us or persons acting on
our behalf are expressly qualified in their entirety by the cautionary
statements set forth above. Forward-looking statements speak only as of the
date they are made, and VIA undertakes no obligation to update publicly any
of these statements in light of new information or future eve
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| SOURCE VIA Pharmaceuticals, Inc. Copyright©2008 PR Newswire. All rights reserved |