Northfield Laboratories Inc. Presentation at FDA/NIH Workshop on Hemoglobin-Based Oxygen Carriers
April 29 2008 - 1:00PM
PR Newswire (US)
EVANSTON, Ill., April 29 /PRNewswire-FirstCall/ -- Northfield
Laboratories Inc. (NASDAQ:NFLD) announced today that Steven A.
Gould, M.D., Chairman and Chief Executive Officer, presented a talk
on the clinical development of PolyHeme(R), the Company's
investigational red cell substitute at an FDA/NIH Workshop on
Hemoglobin-Based Oxygen Carriers. Dr. Gould's talk focused
primarily on data from Northfield's trials in acute blood loss:
earlier trials in hospitalized trauma patients and the recent U.S.
Multicenter Trauma trial. The presentation is available on the
Company website, http://www.northfieldlabs.com/. "The indication we
are seeking for PolyHeme(R), the treatment of life-threatening
hemoglobin levels when blood transfusion is required and red blood
cells are not available or not an option, addresses a critical,
unmet medical need and presents unique challenges for the conduct
of clinical trials," said Dr. Gould. Dr. Gould reviewed data from
the study in hospitalized trauma patients, the results of which
were published in the Journal of the American College of Surgeons
in 2002. The study included 171 patients with acute blood loss who
received up to 20 units of PolyHeme(R), or twice the blood volume
of an adult, during ongoing bleeding. This study demonstrated the
life-sustaining capability of PolyHeme(R) in patients with
life-threatening red blood cell hemoglobin levels compared to
historical controls who refused blood transfusion due to their
religious beliefs. In reviewing the data from the U.S. Multicenter
study, Dr. Gould noted that Northfield's study was logistically
complex, and was the first study of a red cell substitute in the
U.S. to begin at the scene of injury. The study was conducted at 32
Level I trauma centers, enrolled 720 trauma patients, and included
the participation of 300 ambulances and 3500 EMTs in addition to
150 principal investigators and thousands of allied hospital staff.
The study compared the outcomes of patients receiving the current
standard of care, salt water at the scene and during transport,
followed by blood immediately upon arrival at the hospital, and
patients who received PolyHeme(R) for up to a dose of six units or
12 hours following injury. Dr. Gould focused his remarks on results
in two analysis populations, the 714 patients who were analyzed As
Randomized, and the 590 patients who were appropriately enrolled
and treated as specified in the protocol (Per Protocol). The
difference between the two populations was the 124 patients with
major protocol violations, who were inappropriately enrolled or not
treated according to the protocol. Dr. Gould noted that the results
in the Per Protocol population, where all aspects of the protocol
were followed, offer the clearest opportunity to assess a treatment
effect of PolyHeme. These protocol violations had an important
influence on the study results. In the PolyHeme group, there were
more patients with protocol violations, there were more protocol
violations per patient, and more of these patients had predictors
of poor outcomes present prior to treatment. New Data from
Independent Data Monitoring Subcommittee on Cardiac Events In
reviewing safety data from the study, Dr. Gould reviewed the most
commonly reported adverse and serious adverse events, providing new
data on cardiac events. He stated that in order to reconcile the
disparity between the low number of reported myocardial infarctions
(MIs) and the high incidence of abnormal EKGs and elevated cardiac
enzymes, Northfield established an independent Cardiac Subcommittee
of the IDMC to review, based on the available data, the cardiac
profiles of all 720 enrolled patients in a blinded fashion. They
used objective criteria to classify the MIs in the study as
"possible," "probable," "indeterminate," and "absent." More than
half the patients in both study groups had some evidence of
myocardial infarction. [See table.] IDMC Cardiac Subcommittee MI
Analysis PolyHeme(R) Control (n=349) (n=365) Probable MI 42 (12%)
30 (8%) Possible MI 145 (42%) 159 (44%) Total 187 (54%) 189 (52%)
Indeterminate 79 (23%) 112 (31%) Absent MI 83 (24%) 64 (18%) "This
is useful information, which confirms the difficulty of diagnosing
cardiac ischemia in trauma patients," said Dr. Gould. Dr. Gould
concluded his presentation by summarizing the development of
PolyHeme(R). "We believe our studies demonstrate that PolyHeme(R)
offers a survival benefit in cases of life-threatening red blood
cell hemoglobin levels and has an acceptable safety profile and
favorable benefit-to-risk ratio when red blood cells are not
available." About Northfield Laboratories and PolyHeme(R)
Northfield Laboratories Inc. is a leader in developing an
oxygen-carrying red blood cell substitute for the treatment of
life-threatening blood loss, when an oxygen-carrying fluid is
required and red blood cells are not available. Northfield's
product, PolyHeme(R), is under clinical investigation as
oxygen-carrying red blood cell substitute. It is a solution of
chemically modified human hemoglobin that requires no cross
matching and is therefore compatible with all blood types. It has a
shelf life in excess of 12 months. For further information, visit
http://www.northfieldlabs.com/. Forward Looking Statement This
press release may contain forward-looking statements concerning,
among other things, Northfield's future business plans and
strategies and clinical and regulatory developments affecting our
PolyHeme red blood cell substitute product. These forward-looking
statements are identified by the use of such terms as "intends,"
"expects," "plans," "estimates," "anticipates," "should,"
"believes" and similar terms. These forward-looking statements
involve inherent risks and uncertainties. Our actual results may
therefore differ materially from those predicted by the
forward-looking statements because of various factors and possible
events, including the possibility that since the full data from our
Phase III clinical trial have not been submitted to, or reviewed
by, FDA, they may not be sufficient to demonstrate the safety or
effectiveness of PolyHeme, our ability to successfully file a
Biologics License Application, our ability to be granted priority
review of our Biologics License Application, our ability to obtain
FDA approval to market PolyHeme commercially, our need to obtain
additional capital to finance our ongoing business operations and
the construction of an expanded commercial- scale manufacturing
facility, our ability to obtain adequate supplies of raw materials
and to manufacture PolyHeme in commercial quantities, our ability
to market PolyHeme successfully, the possibility that competitors
will develop products that will render PolyHeme obsolete or
non-competitive, our ability to protect our intellectual property
rights, the outcome of certain governmental inquiries and purported
class action lawsuit as described in our most recently filed annual
report on Form 10-K and quarterly report on Form 10-Q, the
possibility that we may be subject to product liability claims and
other legal actions, our dependency on a limited number of key
personnel, the uncertainty of third party reimbursement for our
product and other risks and uncertainties described from time to
time in our periodic reports filed with the Securities and Exchange
Commission, including our most recently filed annual report on Form
10-K and annual report on Form 10-Q. These forward-looking
statements speak only as of the date of this press release. We do
not undertake any obligation to update or publicly release any
revisions to forward-looking statements to reflect events,
circumstances or changes in expectations after the time such
statement is made. All subsequent written and oral forward- looking
statements attributable to Northfield or any person acting on our
behalf are qualified by this cautionary statement. Sophia H.
Twaddell Vice President, Corporate Communications (847) 864-3500
DATASOURCE: Northfield Laboratories Inc. CONTACT: Sophia H.
Twaddell, Vice President, Corporate Communications of Northfield
Laboratories Inc., +1-847-864-3500, Web site:
http://www.northfieldlabs.com/
Copyright
Northfield labs (NASDAQ:NFLD)
Historical Stock Chart
From Oct 2024 to Nov 2024
Northfield labs (NASDAQ:NFLD)
Historical Stock Chart
From Nov 2023 to Nov 2024