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On the hunt for Huntington’s disease therapy
July 2012
SHARING OPTIONS:
DEERFIELD, Ill.—Two leaders in Huntington’s disease
research, global pharmaceutical company H. Lundbeck AS and not-for-profit
biomedical research organization CHDI Foundation Inc., have joined forces to
conduct preclinical studies on a targeted therapy for the neurodegenerative
condition.
The partners announced this endeavor in May, coinciding with
HD Awareness Month, and it is part of Lundbeck’s HD Research Initiative, a
commitment announced in 2010 to identify and ultimately commercialize therapies
that may slow or halt the progression of HD. The initiative is driven by
collaborations with like-minded academic institutions, research organizations
and companies.
Although the collaboration is a first for the two parties,
CHDI is no stranger to partnerships in HD research. The organization actively
enables HD research by collaborating with research organizations and
pharmaceutical companies conducting promising research, often providing
financial support. CHDI’s activities include exploratory biology, clinical
studies and trials and educational workshops.
In Lundbeck, CHDI gains a partner that is well established
in central nervous system drug research and development, said the
organization’s vice president of translational biology, Ignacio Munoz-Sanjuan,
in a press release announcing the deal.
“Lundbeck has a proven track record of not only bringing new
therapies to market, but also working to support the needs of their patient
communities,” Munoz-Sanjuan added. “We hope this research collaboration
provides a stepping stone for future therapies that slow the progression of
HD.”
But Lundbeck “can’t do research all by ourselves,” says
Stevin Zorn, executive vice president for Lundbeck Research USA. “That is only
part of how we do business. In a number of interactions with CHDI in the past
few years, we developed a deep respect for each other. CHDI is very closely
focused on biomedical research, and since we don’t have much experience in that
area, we thought getting together would benefit us both by bringing something
they could help us advance.”
As part of the collaboration, CHDI will conduct preclinical
studies on a Lundbeck investigative compound. The research will focus on the
compound’s effect on P2X receptors that may be involved in HD. P2X receptors
are membrane ion channels that open in response to the binding of extracellular
adenosine triphosphate (ATP), the molecule that cells use for energy to power
all their processes.
In 2011, Lundbeck and the University of Massachusetts
Medical School began to investigate RNAi-based therapies to suppress the
production of mutant huntingtin (mHtt), the abnormal protein that causes HD.
“We worked with scientists to study RNAi-based therapy that
should provide a way of suppressing the protein mHtt, which could potentially
change the course of this illness,” says Zorin.
According to the partners, the study results will influence
future research into this and other compounds for HD. Currently available
therapies for HD treat only its symptoms.
HD is a neurodegenerative genetic disorder that affects
muscle coordination and leads to cognitive decline and psychiatric problems.
These symptoms can vary from patient to patient. The survival time after the
onset of symptoms can range from 10 to 30 years.
Complications such as pneumonia, heart disease and physical
injury contribute to that figure. There is no cure for HD, and full-time care
is usually required in the later stages of the disease.
“There are about 20,000 people who suffer from HD. There is
no cure, and the disease can be devastating. Coming up with an effective
treatment for this illness could have a fairly robust impact on society,” says
Zorin.
Code: E071224 Back |
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