
HepaLife™ Enters Into New Cooperative Research and
Development Agreement with U.S. Government Agency
Boston, MA – November 27, 2007 - HepaLife
Technologies, Inc. (OTCBB: HPLF) (FWB: HL1) (WKN: 500625) today announced
that the Company has entered into a new Cooperative Research and
Development Agreement (CRADA) with the U.S. Department of Agriculture,
Agricultural Research Service (USDA, ARS) for further optimization
of HepaLife’s PICM-19 liver stem cell line for application
in the first-of-its-kind bioartificial liver device.
Incorporating the PICM-19 cell line, HepaLife is developing the
first-of-its-kind bioartificial liver. HepaLife's bioartificial liver,
currently under development, is designed to operate outside the patient's
body. The bioartificial liver is envisioned to mimic important functions
of the human liver by circulating the patient's blood inside the
device, where it is exposed to HepaLife's PICM-19 liver stem cells,
thus processing the patient's blood-plasma by removing toxins, enhancing
metabolic function, and ultimately, imitating the liver's natural
function.
“The execution of our new CRADA and the announcement of our
exclusive worldwide PICM-19 license agreement with the USDA earlier
this month, together mark important objectives for HepaLife and for
the development of our bioartificial liver device,” stated
Mr. Frank Menzler, President and CEO of HepaLife. “We continue
to achieve the goals set in our business plan, both from a corporate
and scientific perspective, and are moving closer to initial in-vivo
trials.”
Intended for the treatment of liver failure, the HepaLife™ Bioartificial
Liver device consists of three basic components: (1) a plasma filter,
separating the patient’s blood into blood plasma and blood
cells; (2) the bioreactor, a unit filled with PICM-19 cells which
biologically mimic the liver’s function; and (3), the HepaDrive™,
a perfusion system for pumping the patient's plasma through the bioreactor
while controlling gas supply and temperature for best possible performance
of the cells.
ABOUT HEPALIFE TECHNOLOGIES, INC.
HepaLife Technologies, Inc. (OTCBB: HPLF - News; FWB: HL1) (WKN:
500625) is a developer of cell-based medical technologies addressing
prevalent human health concerns.
Current cell-based technologies under development by HepaLife include
1) the first-of-its-kind artificial liver device, 2) proprietary
in-vitro toxicology and pre-clinical drug testing platforms, and
3) novel cell-culture based vaccine production methods for the manufacture
of vaccines against H5N1 avian influenza and other viruses.
For additional information, please visit www.hepalife.com.
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http://www.hepalife.com/investor-alerts.php
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http://www.hepalife.com/20071127-1.html.php
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products intended to diagnose, treat, prevent or cure any disease.
The statements contained in this press release regarding our on going
research and development and the results attained by us to-date have
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be no assurance that further research and development, and /or whether
clinical trial results, if any, will validate and support the results
of our preliminary research and studies. Further, there can be no
assurance that the necessary regulatory approvals will be obtained
or that HepaLife will be able to develop commercially viable products
on the basis of its technologies. In addition, other factors that
could cause actual results to differ materially are discussed in
the Company's most recent Form 10-Q and Form 10-K filings with the
Securities and Exchange Commission. These reports and filings may
be inspected and copied at the Public Reference Room maintained by
the U.S. Securities & Exchange Commission at 100 F Street, N.E.,
Washington, D.C. 20549. You can obtain information about operation
of the Public Reference Room by calling the U.S. Securities & Exchange
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The Company makes no commitment to publicly release the results of
any revisions to these forward looking statements that may be made
to reflect the events or circumstances after the date hereof or to
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