AstraZeneca and AVANIR Announce Global Alliance to Discover and Develop Novel Reverse Cholesterol Transport Enhancing Compounds
July 11 2005 - 8:15AM
Business Wire
AstraZeneca PLC today announced an exclusive global licensing and
research collaboration agreement with AVANIR Pharmaceuticals
(AMEX:AVN) to discover, develop and commercialise Reverse
Cholesterol Transport (RCT) enhancing compounds for the treatment
of cardiovascular disease. RCT enhancing compounds are designed to
directly increase the flow of lipids from blood vessel walls by
promoting a natural process known as Reverse Cholesterol Transport.
Compounds that enhance this pathway may potentially reverse
existing vascular disease in comparison to current agents that have
to date only been shown to prevent disease progression.
"AstraZeneca has a strategic commitment to find new treatments for
dyslipidaemia, and Reverse Cholesterol Transport is an exciting
therapeutic area for us. We wish to build on our existing strengths
and this alliance will open up new opportunities for AstraZeneca in
the treatment of cardiovascular disease," said Gunnar Olsson, Head
of the Cardiovascular Therapy Area, AstraZeneca. Under the terms of
the agreement, AVANIR will receive an upfront payment of $10
million. In addition, AVANIR is eligible for milestone payments
totaling $330 million, contingent upon achievement of development
and regulatory milestones and on achievement of sales targets,
together with the payment of stepped royalties rising from single
digit to low double digit rates, dependent on sales achieved.
AstraZeneca will assume responsibility for development and for both
product discovery and development costs, with both parties
contributing scientific expertise in the research collaboration.
"Reverse cholesterol transport is an attractive target for the
development of drugs for cardiovascular disease. AstraZeneca has a
long-standing record of achievement in development and
commercialization in this area. Their leadership in cardiovascular
therapies makes them the ideal partner to maximize the potential of
this programme," said Marty Emanuele, Ph.D., Vice President of
Business Development, AVANIR Pharmaceuticals. RCT is a natural
process that involves the flow of cholesterol from tissues,
including the walls of blood vessels, and its subsequent transport
to the liver for metabolism and removal from the body. The process
is complex, involving several steps, and a variety of specialized
transporter molecules and carrier proteins to take cholesterol out
of body tissues into the liver. Once cholesterol is taken up by the
liver, it can then be transported to the gall bladder for
excretion. Enhancement of the natural reverse cholesterol pathway
is promising because it is likely to provide a more effective
process for protecting blood vessels from vascular disease induced
by abnormal blood lipids. Currently available agents are effective
in prevention of the fuller development of additional lipid rich
plaque, but have yet to be proved effective in regressing or
decreasing the existing plaque burden. Enhancing the RCT pathway
may be more effective at reducing pre-existing vascular disease.
AstraZeneca is a major international healthcare business engaged in
the research, development, manufacture and marketing of
prescription pharmaceuticals and the supply of healthcare services.
It is one of the world's leading pharmaceutical companies with
healthcare sales of over $21.4 billion and leading positions in
sales of gastrointestinal, cardiovascular, respiratory, oncology
and neuroscience products. In the United States, AstraZeneca is a
$9.6 billion healthcare business with more than 12,000 employees.
AstraZeneca is listed in the Dow Jones Sustainability Index
(Global) as well as the FTSE4Good Index. For more information about
AstraZeneca, please visit: http://www.astrazeneca-us.com/ AVANIR
Pharmaceuticals is a pharmaceutical company focused on developing
and commercializing novel therapeutic products for the treatment of
chronic diseases. AVANIR's product candidates address therapeutic
markets that include central nervous system and cardiovascular
disorders, inflammation, and infectious disease. AVANIR recently
submitted to the FDA the last modules of its "rolling" new drug
application for Neurodex(TM) for the treatment of pseudobulbar
affect. Additionally, AVANIR has initiated a Phase 3 clinical trial
of Neurodex in patients with diabetic neuropathic pain. Recently,
AVANIR partnered its preclinical research and development program
for inflammatory disease with Novartis. The Company's first
commercialized product, Abreva(R), is marketed in North America by
GlaxoSmithKline Consumer Healthcare and is the leading
over-the-counter product for the treatment of cold sores. Further
information about AVANIR can be found at www.avanir.com. Except for
the historical information presented herein, matters discussed in
this press release contain forward-looking statements that are
subject to certain risks and uncertainties that could cause actual
results to differ materially from any future results, performance
or achievements expressed or implied by such statements. Statements
that are not historical facts, including statements that are
preceded by, followed by, or that include such words as "estimate,"
"anticipate," "believe," "plan" or "expect" or similar statements
are forward-looking statements. Risks and uncertainties for AVANIR
Pharmaceuticals include risks associated with product discovery and
development as well as risks shown in AVANIR's most recent Annual
Report on Form 10-K and Quarterly Report on Form 10-Q and from
time-to-time in other publicly available information regarding the
company. Copies of such information are available from AVANIR upon
request. Such publicly available information sets forth many risks
and uncertainties related to AVANIR's business and technology. Our
anti-inflammation research program is in the early stages of
development and competes with other research approaches and
compounds under development by large pharmaceutical and
biotechnology companies. Preclinical research findings are not
always supportable by evidence obtained from clinical trials. Final
review decisions made by the FDA and other regulatory agencies
concerning clinical trial results are unpredictable and outside the
influence and/or control of the Company. The company disclaims any
intent or obligations to update these forward-looking statements.
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