IR BioSciences Holdings, Inc. to Collaborate with Leading Clinical Services Company to Evaluate Radilex(TM) in Low-Level Radiati
26 February 2007 - 11:00PM
PR Newswire (US)
Parties to Explore Applications in Area of Oncology SCOTTSDALE,
Ariz., Feb. 26 /PRNewswire-FirstCall/ -- ImmuneRegen BioSciences, a
wholly owned subsidiary of IR BioSciences Holdings, Inc. (OTC:IRBO)
(BULLETIN BOARD: IRBO) announced today that it has entered into an
agreement with The Translational Genomics Research Institute
(TGen), a non- profit organization focused on developing earlier
diagnostics and smarter treatments. The parties will collaborate to
identify and develop innovative solutions to mitigate the
side-effects of radiation therapy in cancer patients using
ImmuneRegen's proprietary compound Radilex(TM). The parties believe
that the solutions, based on completed and ongoing animal and cell
culture studies, may also mitigate the effects of non-therapeutic
radiation exposure. Radilex(TM) has already demonstrated through
animal studies the potential for treatment of acute radiation
syndrome (ARS) following lethal doses of radiation. Non-therapeutic
radiation exposures might result following the explosion of a
radiological dispersion device ("dirty bomb") or nuclear weapon.
"It is our mission to participate in the identification and
accelerated development of treatment modalities for cancer
patients," said Stephen Gately, Director, Non-clinical Development
at TD2. "We are enthusiastic and pleased to be working with
ImmuneRegen on these promising applications for bio-defense and
toxic therapy radiation exposure." "Based upon the promising
results we have seen with Radilex to date in high-dose radiation
exposure, we believe that the potential exists to apply the
compound to the treatment of low-level radiation exposure, which
represents a much larger market. We are excited to explore a number
of potential applications in the area of oncology, this being the
first," said Michael Wilhelm, ImmuneRegen CEO. Recently,
ImmuneRegen announced that it had retained Battelle, the world's
largest independent research and development organization, as an
accredited testing facility. Battelle will perform additional
specialized laboratory services supporting additional studies of
the biological and radiological effectiveness of Radilex(TM). About
TD2 TGen Drug Development Services (TD2), helps investigators from
research institutions, biotech and pharmaceutical companies
evaluate the efficacy of their drug candidate by using preclinical
models, genomic tools and coordination of Phase I clinical trials
at various clinical facilities, including Mayo Clinic Scottsdale,
Scottsdale Healthcare, the Arizona Cancer Center, and U.S.
Oncology. TD2 also provides central coordination of an
international team of investigators who are conducting studies in
patients with pancreatic cancer. Although initially focused in
oncology, TD2 expects to expand its capabilities to other disease
areas including neurological diseases and diabetes. About TGen The
Translational Genomics Research Institute (TGen), a non-profit
501(c)(3) organization, is focused on developing earlier
diagnostics and smarter treatments. Translational genomics research
is a relatively new field employing innovative advances arising
from the Human Genome Project and applying them to the development
of diagnostics, prognostics and therapies for cancer, neurological
disorders, diabetes and other complex diseases. TGen's research is
based on personalized medicine and the institute plans to
accomplish its goals through robust and disease-focused research.
About Radilex(TM) and Viprovex(TM) Radilex(TM) is the trade name
used in referring to formulations of Homspera for potential
indications for treatment of exposure to ionizing radiation.
Viprovex(TM) is the trade name used in referring to formulations of
Homspera for potential indications for treatment of viral and
bacterial infections. Homspera is a generic name used by the
Company to describe the synthetic peptide Sar9, Met
(O2)11-Substance P. Sar9, Met (O2)11-Substance P is an analog of
the naturally occurring human neuropeptide Substance P, which can
be found throughout the body, including in the airways of humans
and many other species. All of the Company's research and
development efforts are early, pre-clinical stage and Homspera, as
Viprovex(TM) and Radilex(TM), has only undergone exploratory
studies to evaluate its biological activity in small animals. About
ImmuneRegen BioSciences, Inc. IR BioSciences Holdings, Inc.,
through its wholly-owned subsidiary ImmuneRegen BioSciences, Inc.,
is a development stage biotechnology company focused on the
research and development of Homspera(TM) and its derivatives
Radilex(TM) and Viprovex(TM), which are designed to be used as
countermeasures for multiple homeland security bioterrorism
threats. Homspera is derived from Substance P, a naturally
occurring peptide immunomodulator and homeostatic compound with the
dual effect of improving pulmonary function and the stimulation of
the human immune system. For more information, please visit the
company's website at http://www.immuneregen.com/. Statements about
the Company's future expectations, including statements about the
potential for the Company's drug candidates, science and
technology, and all other statements in this press release other
than historical facts, are "forward-looking statements" within the
meaning of Section 27A of the Securities Act of 1933, Section 21E
of the Securities Exchange Act of 1934, and as that term is defined
in the Private Securities Litigation Reform Act of 1995. The
Company intends that such forward-looking statements be subject to
the safe harbors created thereby. These future events may not occur
as and when expected, if at all, and, together with the Company's
business, are subject to various risks and uncertainties. The
Company's actual results could differ materially from expected
results as a result of a number of factors, including the fact that
preliminary results involved only a small number of test mice, the
subsequent investigations were limited in scope, the uncertainties
inherent in research and development collaborations, pre- clinical
and clinical trials and product development programs, (including,
but not limited to the fact that future results or research and
development efforts may prove less encouraging than current results
or cause side effects not observed in current pre-clinical trials)
the evaluation of potential opportunities, the level of corporate
expenditures and monies available for further studies, capital
market conditions, and others set forth in the Company's periodic
report on Form 10-QSB for the three months ended September 30, 2006
and on Form 10-KSB for the twelve months ended December 31, 2005 as
filed with the Securities and Exchange Commission. There are no
guarantees that any of the Company's proposed products will prove
to be commercially successful. The Company undertakes no duty to
update forward-looking statements. MEDIA CONTACT: W. Jason Grimley
Spelling Communications 310-477-9500 INVESTOR CONTACT: Josh
Reynolds CEOcast, Inc. 212-732-4300 DATASOURCE: ImmuneRegen
CONTACT: Media - W. Jason Grimley, Spelling Communications,
+1-310-477-9500, , or Investor - Josh Reynolds, CEOcast, Inc.,
+1-212-732-4300, , both for ImmuneRegen BioSciences, Inc. Web site:
http://www.immuneregen.com/
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