s included in this press release, particularly
those anticipating future financial performance, clinical and business
prospects for our clinical compound for neuropathic pain, Bicifadine, and
for our pre-clinical compounds for hepatitis C from our XTL-DOS program,
growth and operating strategies and similar matters, may be forward-looking
statements that involve a number of risks and uncertainties. For those
statements, we claim the protection of the safe harbor for forward-looking
statements contained in the Private Securities Litigation Reform Act of
1995. Among the factors that could cause our actual results to differ
materially are the following: our ability to start a clinical trial with
Bicifadine in 2007 and our ability to successfully complete cost-effective
pre-clinical trials for our DOS program, both of which will directly impact
our ability to continue to fund our operations; our ability to meet
anticipated development timelines for all of our drug candidates due to
recruitment, clinical trial results, manufacturing capabilities or other
factors; and other risk factors identified from time to time in our reports
filed with the Securities and Exchange Commission and the London Stock
Exchange, including our annual report on Form 20-F filed with the
Securities and Exchange Commission on March 23, 2007. Any forward-looking
statements set forth in this press release speak only as of the date of
this press release. We do not intend to update any of these forward-looking
statements to reflect events or circumstances that occur after the date
hereof. This press release and prior releases are available at
http://www.xtlbio.com. The information in our website is not incorporated
by reference into this press release and is included as an inactive textual
reference only.
XTL BIOPHARMACEUTICALS LTD.
(A Development Stage Company)
Consolidated Balance Sheets
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SOURCE XTL Biopharmaceuticals Ltd
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