LINCOLN, R.I.,
'As we enter 2008, our initial efforts will be on fund raising efforts,
and advancing MCT-125 in our planned Phase IIb trial,' said
The foregoing event is further described in a Current Report on Form 8-K
that MultiCell Technologies filed on
MultiCell Technologies, Inc. is a biopharmaceutical company developing new therapeutics including:
MCT-125 for the treatment of primary fatigue in MS patients.
MCT-175 for the treatment of relapsing-remitting MS.
MCT-465 for the treatment of TLR3 positive breast cancers.
MCT-475 for the treatment of TLR3 positive cervical cancers.
MultiCell also sells and/or licenses immortalized human liver cells to the pharmaceutical industry and holds patents on the Sybiol(R) synthetic bio-liver device and liver-derived adult human stem cells.
For more information about MultiCell Technologies, please visit http://www.multicelltech.com
Caution Regarding Forward-Looking Statements
Any statements in this press release about MultiCell's expectations,
beliefs, plans, objectives, assumptions or future events or performance are
not historical facts and are forward-looking statements for purposes of the
Private Securities Litigation Reform Act of 1995 (the 'Act'). These
statements are often, but not always, made through the use of words or phrases
such as 'believe,' 'will,' 'expect,' 'anticipate,' 'estimate,' 'intend,'
'plan,' 'forecast,' 'could,' and 'would.' Examples of such forward looking
statements include statements regarding the timing, design, scope, and
anticipated results of our clinical development of MCT-125 and the likelihood
of the successful conclusion of current financing and business negotiations.
MultiCell bases these forward-looking statements on current expectations about
future events. They involve known and unknown risks, uncertainties and
assumptions that may cause actual results, levels of activity, performance or
achievements to differ materially from those expressed or implied by any
forward-looking statement. Some of the risks, uncertainties and assumptions
that could cause actual results to differ materially from estimates or
projections in the forward-looking statement include, but are not limited to,
the risk that we might not achieve our anticipated clinical development
milestones, receive regulatory approval, or successfully commercialize MCT-125
as expected, the market for our products will not grow as expected, the risk
that we will not successfully conclude discussions with prospective partners
or complete our fund raising efforts and the risk that our products will not
achieve expectations. For additional information about risks and
uncertainties MultiCell faces, see documents MultiCell files with the SEC,
including MultiCell's report on Form 10-KSB for the fiscal year ended
SOURCE MultiCell Technologies, Inc.
