Sep 15, 2009 Press Release for Alnylam
Alnylam and Medtronic Present New Late-Stage Pre-clinical Data on ALN-HTT, an RNAi Therapeutic for the Treatment of Huntington's Disease
Sep 15, 2009
The newly presented pre-clinical research, performed in collaboration
with Professor
“We are very pleased with these promising results in our Huntington’s
disease program, as it continues to represent an exciting opportunity to
combine innovative medicines with our state-of-the-art drug device
delivery technology in an area of extreme unmet medical need,” said
Gregory Stewart Ph.D., Director of CNS Drug Therapy R&D at
technologies could provide a novel treatment strategy for this
devastating neurodegenerative disease.”
The new pre-clinical studies presented at this meeting employed direct delivery of ALN-HTT to the striatum using implantable infusion pumps and convection-enhanced delivery (CED), or continuous infusion under positive pressure. Specifically, the new data showed that direct CNS administration of ALN-HTT resulted in:
- broad distribution of the siRNA across the CNS, including the striatum and surrounding brain regions;
- silencing of the huntingtin gene mRNA by an average of approximately 45% in the putamen following continuous infusion over seven days, as well as reductions in the levels of huntingtin protein as demonstrated by immunohistochemistry;
- silencing of the huntingtin gene messenger RNA (mRNA) in the CNS at significant distances from the infusion site; and,
- a safe and well tolerated profile following continuous infusion over 28 consecutive days, with no clinical abnormalities, neurological behavioral signs, and no clinically significant findings in histopathological examination of the brain.
“We are very excited by our new findings as they represent a major leap
forward in our Huntington’s disease program across multiple dimensions,”
said
This research was done with the laboratory of
In
About Huntington’s Disease
Huntington’s disease is an autosomal dominant neurodegenerative genetic disease that afflicts approximately 30,000 patients in the U.S., with an estimated 200,000 additional patients having a 50% risk of developing the disease. The average lifespan for patients after onset is approximately 10 to 20 years. There are currently no effective therapies available for the treatment of Huntington’s disease.
About RNA Interference (RNAi)
RNAi (RNA interference) is a revolution in biology, representing a breakthrough in understanding how genes are turned on and off in cells, and a completely new approach to drug discovery and development. Its discovery has been heralded as “a major scientific breakthrough that happens once every decade or so,” and represents one of the most promising and rapidly advancing frontiers in biology and drug discovery today which was awarded the 2006 Nobel Prize for Physiology or Medicine. RNAi is a natural process of gene silencing that occurs in organisms ranging from plants to mammals. By harnessing the natural biological process of RNAi occurring in our cells, the creation of a major new class of medicines, known as RNAi therapeutics, is on the horizon. Small interfering RNAs (siRNAs), the molecules that mediate RNAi and comprise Alnylam’s RNAi therapeutic platform, target the cause of diseases by potently silencing specific mRNAs, thereby preventing disease-causing proteins from being made. RNAi therapeutics have the potential to treat disease and help patients in a fundamentally new way.
About
About
Alnylam is a biopharmaceutical company developing novel therapeutics
based on RNA interference, or RNAi. The company is applying its
therapeutic expertise in RNAi to address significant medical needs, many
of which cannot effectively be addressed with small molecules or
antibodies, the current major classes of drugs. Alnylam is leading the
translation of RNAi as a new class of innovative medicines with
peer-reviewed research efforts published in the world’s top scientific
journals including Nature, Nature Medicine, and Cell.
The company is leveraging these capabilities to build a broad pipeline
of RNAi therapeutics; its most advanced program is in Phase II human
clinical trials for the treatment of respiratory syncytial virus (RSV)
infection and is partnered with Cubist and Kyowa Hakko. In addition, the
company is developing RNAi therapeutics for the treatment of a wide
range of disease areas, including liver cancers, hypercholesterolemia,
Huntington’s disease, and TTR amyloidosis. The company’s leadership
position in fundamental patents, technology, and know-how relating to
RNAi has enabled it to form major alliances with leading companies
including
Medtronic Forward Looking Statement
Any forward-looking statements are subject to risks and uncertainties
such as those described in Medtronic’s Annual Report on Form 10-K for
the year ended
Alnylam Forward-Looking Statement
Various statements in this release concerning Alnylam’s future
expectations, plans and prospects, constitute forward-looking statements
for the purposes of the safe harbor provisions under The Private
Securities Litigation Reform Act of 1995. Actual results may differ
materially from those indicated by these forward-looking statements as a
result of various important factors, including the company’s ability to
successfully research and develop ALN-HTT, including the ability to
achieve acceptable safety and efficacy results in humans, as well as
those risks more fully discussed in the “Risk Factors” section of its
most recent quarterly report on Form 10-Q on file with the
Source:
Alnylam Pharmaceuticals, Inc.
Cynthia Clayton (Investors),
617-551-8207
or
Yates Public Relations
Kathryn Morris
(Media), 845-635-9828
or
Medtronic, Inc.
Jeff
Warren, 763-505-2696
Investors Relations
or
Chuck
Grothaus, 763-505-2614
Public Relations
For Media Inquiries, please contact:
Christine Akinc
Chief Corporate Communications Officer media@alnylam.com 617-682-4340
For Investor Inquiries, please contact:
Josh Brodsky
VP, Investor Relations & Corporate Communications investors@alnylam.com 617-551-8276
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