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Factors that may cause actual results to differ materially from current expectations include, but are not limited to:
* our ability to obtain necessary financing;
* our ability to control our operating expenses;
* our ability to recruit and enroll patients for the CEA, ACS and FDG-PET
clinical trials;
* our ability to successfully complete our clinical trials of VIA-2291 on
expected timetables and the outcomes of such clinical trials;
* the results of our clinical trials, including without limitation, with
respect to the safety and efficacy of VIA-2291;
* 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 the heading "Risk Factors" in our
Quarterly Report on Form 10-Q for the quarter ended June 30, 2007 on
file with the SEC and in our Form S3 Amendment No. 3 filed with the SEC
October 15, 2007.
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 o
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