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Accelerated development
June 2012
SHARING OPTIONS:
WILMINGTON, Del.—Global biopharmaceutical AstraZeneca PLC
and New Haven, Conn.-based private biotech firm Axerion Therapeutics Inc. have
joined forces to develop an effective treatment for Alzheimer’s disease.
Axerion and Gaithersburg, Md.-based MedImmune, the global
biologics arm of AstraZeneca, announced May 1 that they have entered into a
research collaboration and sublicense arrangement to develop and commercialize
a biologic approach for the treatment of Alzheimer’s.
The agreement with Axerion is the first collaboration signed
within the new Neuroscience Innovative Medicines Unit that AstraZeneca
announced in February 2012. Under this model, AstraZeneca and MedImmune will
conduct neuroscience discovery research and early development for small and
large molecules by tapping into the best available external science and sharing
cost, risk and reward with other research partners active in psychiatry,
neurology and pain research.
Under the terms of the agreement, Axerion has granted
AstraZeneca’s unit an exclusive sublicense to research, develop and
commercialize a preclinical biologic that targets the binding of A-beta
oligimers to prion proteins. The license is based on research conducted by Dr.
Stephen Strittmatter, and the associated intellectual property is exclusively
licensed to Axerion from Yale University.
In exchange, the AstraZeneca unit will provide Axerion with
certain upfront and milestone payments plus research and development funding
during the time both companies are working together on the program.
Additionally, Axerion will earn royalties on product sales. The financial terms
of the deal have not been disclosed.
The two companies will collaborate to develop a biologic
approach that blocks the toxic effects of amyloid-beta (A-beta) mediated
through binding of A-beta oligomers to cellular prion protein in the brain,
according to AstraZeneca. This drug development effort will build on published
preclinical results which demonstrate that cellular prion protein mediates
A-beta oligomer-induced memory dysfunction and synaptic toxicity, and that
inhibition of this interaction can have favorable therapeutic effects. Directly
targeting toxic A-beta oligomer binding has the potential to provide superior
safety and efficacy versus agents that affect amyloid processing or clearance.
The joint project is in the preclinical stage and expected
to remain there in the next three to five years. If all goes well, human trials
will follow, McBrinn says. Past biologic experiments on mouse models with
Alzheimer’s have been successful.
Michael Poole, head of the NIMU, stated in a news release,
“A close collaboration with Axerion in this area of breaking science will
greatly enhance our chances of bringing a medicine to market for people with
Alzheimer’s disease. This biologic approach is an example of the promising
science that fuels our commitment to neuroscience research.”
Sylvia McBrinn, Axerion’s CEO and president, added, “We are
confident that this collaboration will accelerate the development of an
urgently needed therapy for Alzheimer’s disease … It is our hope that this
collaboration will advance a novel therapy that works quite differently from
the Alzheimer’s drug candidates currently in development.”
The novel therapy is actually an injectable, McBrinn says,
which differs from the usual small-molecule approach of taking pills.
“Keep in mind,” says McBrinn, “the solution to alleviating
the symptoms of Alzheimer’s could consist of a cocktail of therapies. The
problem is, nothing will be 100-percent effective.”
An estimated 5.1 million people in the United States are
living with Alzheimer’s, according to the U.S. National Institute of Health
(NIH), which also predicts that by the year 2050, 11 million additional people
in the United States—and 115.4 million worldwide—will have Alzheimer’s. The NIH
also estimates $1.1 trillion will be spent in the United States on caregiving
costs connected to Alzheimer’s patients, compared with $200 billion this year.
President Obama signed the National Alzheimer’s Project Act
into law in January 2011, which called for a coordinated national plan to fight
Alzheimer’s, including a push for a $156 million increase in funding for
Alzheimer’s research over the next two years—in addition to the $450 million
already being spent.
Code: E061224 Back |
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