
HepaLife™ to Present New Bioartificial Liver Device
Data at Major National Scientific Conference
Boston, MA – March 25, 2008 – HepaLife
Technologies, Inc. (OTCBB: HPLF) (FWB: HL1) (WKN: 500625) today announced
that the Company will present new data from ongoing research and
development of its artificial liver device technology in three presentations
at the 54th Annual Meeting of the American Society of Artificial
Internal Organs (ASAIO), June 19-21, 2008. The conference, “Concept
to Commercialization of Organ Replacement & Repair Therapies”,
will be held at the Hilton Hotel in San Francisco, California.
Among industry insiders and researchers, the ASAIO Annual Meeting
is reputed as the premier scientific and business gathering for new
discoveries in the development of artificial internal organ technologies.
Notably, ASAIO members include the inventors of the artificial kidney,
the heart-lung machine that made open heart surgery possible, and
the first artificial heart.
“It’s an honor to be invited to present our exciting
technology at this prestigious meeting,” stated Mr. Frank Menzler,
President and CEO of HepaLife Technologies, Inc. “In recent
months, our research team has made tremendous progress on both the
hardware components of our bioartificial liver device, and our patented
PICM-19 liver stem cell line which is seeded inside the device to
mimic the biological functions of the liver. We very much look forward
to sharing new data from our bioartificial liver program with the
scientific community.”
HepaLife’s presentations at the ASAIO Annual Meeting include:
1. “Bioartificial Liver Device Utilizing the PICM-19 Porcine
Liver Stem Cell Line” presented by F. Menzler, President & CEO
HepaLife Technologies, Inc.
2. “Morphology and Metabolic Activity of a Porcine Liver Stem
Cell Line (PICM-19) Maintained in a Multicompartment Hollow Fiber
Bioreactor for Two Weeks” presented by R. Willard, USDA, ARS-ABBL
3. “Characterization of PICM-19H Porcine Liver Stem Cell Line
for Potential Use in a Bioartificial Liver” presented by R.
Willard, USDA, ARS-ABBL
HepaLife™ Bioartificial Liver
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 the patented PICM-19
liver stem cell line which biologically mimics 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.
Positive results from recent in-vitro tests of HepaLife's proprietary
bioartificial liver were announced last month. Researchers 'seeded'
the Company's patented PICM-19 liver cells inside its artificial
liver device and favorably demonstrated the important ability to
reduce levels of toxic ammonia by 75% in fewer than 24 hours, a feature
considered necessary to the successful treatment of acute liver failure
using an artificial liver. In contrast to HepaLife's early preclinical
results, published in-vivo data from clinical trials of systems utilizing
liver cells other than the Company's PICM-19, have only reported
ammonia reduction levels between 0 to 44%.
American Society of Artificial Internal Organs (ASAIO)
The Annual Conference of the American Society of Artificial Internal
Organs (ASAIO) draws up to 800 attendees with a broad range of primary
interests. This Conference includes presentations from over 400 speakers
from more than a dozen countries. ASAIO’s Conference is unique
in that it provides a forum for individual researchers to present
not only to fellow investigators, but also to members of industry
and to government representatives who will be involved in regulatory
affairs as the projects are developed into the production of clinical
devices. Among ASAIO’s members are the inventors of the artificial
kidney, the heart-lung machine that made open heart surgery possible
and the first artificial heart.
ABOUT HEPALIFE TECHNOLOGIES, INC.
Based in Boston, Massachusetts, HepaLife Technologies, Inc. (OTCBB:
HPLF) (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.
To receive future press releases via email, please visit:
http://www.hepalife.com/investor-alerts.php
To view the full HTML text of this release, please visit:
http://hepalife.com/press_releases/20080325-1.html.php
# # # #
Legal
Notice Regarding Forward-Looking Statements
No statement herein should be considered an offer
or a solicitation of an offer for the purchase or sale of any securities.
This release contains forward-looking statements that are based upon
current expectations or beliefs, as well as a number of assumptions
about future events. Although the Company believes that the expectations
reflected in the forward-looking statements and the assumptions upon
which they are based are reasonable, it can give no assurance that
such expectations and assumptions will prove to have been correct.
Forward-looking statements, which involve assumptions and describe
our future plans, strategies, and expectations, are generally identifiable
by use of the words “may,” “will,” “should,” “could,” “expect,” “anticipate,”
“estimate,” “believe,” “intend,” or “project” or
the negative of these words or other variations on these words or
comparable terminology. The reader is cautioned not to put undue
reliance on these forward-looking statements, as these statements
are subject to numerous factors and uncertainties, including but
not limited to adverse economic conditions, intense competition,
lack of meaningful research results, entry of new competitors and
products, adverse federal, state and local government regulation,
inadequate capital, unexpected costs and operating deficits, increases
in general and administrative costs, termination of contracts or
agreements, technological obsolescence of the Company's products,
technical problems with the Company's research and products, price
increases for supplies and components, litigation and administrative
proceedings involving the Company, the possible acquisition of new
businesses or technologies that result in operating losses or that
do not perform as anticipated, unanticipated losses, the possible
fluctuation and volatility of the Company's operating results, financial
condition and stock price, losses incurred in litigating and settling
cases, dilution in the Company's ownership of its business, adverse
publicity and news coverage, inability to carry out research, development
and commercialization plans, loss or retirement of key executives
and research scientists, changes in interest rates, inflationary
factors, and other specific risks. We currently have no commercial
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
not been evaluated by the Food and Drug Administration. There can
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
Commission at 1-800-SEC-0330. The U.S. Securities & Exchange
Commission also maintains an Internet site that contains reports,
proxy and information statements, and other information regarding
issuers that file electronically with the U.S. Securities & Exchange
Commission at http://www.sec.gov.
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
reflect the occurrence of unanticipated events. |