Alnylam Pharmaceuticals, Inc. (Nasdaq: ALNY), a leading RNAi
therapeutics company, announced today that the United States Patent and
Trademark Office (USPTO) has awarded a Notice of Allowance for the
"Soutschek and Manoharan” patent (Application No. 10/916,185), which
covers certain chemically modified siRNAs of any length directed to any
target, including siRNAs with sterol conjugates for in vivo
delivery. The new patent is based on the ground-breaking research by
Alnylam scientists on systemic delivery of RNAi therapeutics as
documented in Soutschek et al. (Nature 432, 173-178 (11
November 2004)).
"We are very pleased with the USPTO’s allowance of claims from this
patent, as it heralds a new wave of Alnylam-derived patents based on the
pioneering research efforts of our scientists on in vivo delivery
of RNAi therapeutics. Importantly, these new patents significantly
broaden the scope and extend the horizon of our fundamental intellectual
property, including patents from the Crooke, Glover, Kreutzer-Limmer,
Tuschl I, and Tuschl II patent families,” said Barry Greene, President
and Chief Operating Officer of Alnylam. "The Soutschek and Manoharan
patent family derives from one of the most important scientific
publications in the field of RNAi therapeutics, as published in the
prestigious journal Nature in 2004. This landmark paper was the
first to show RNAi-mediated gene silencing in mammals with systemic
delivery of chemically modified RNAi therapeutics in vivo.”
Alnylam’s IP position is comprised of fundamental, chemistry, delivery,
and target patents and patent applications that the company believes are
necessary for the development and commercialization of RNAi
therapeutics. In aggregate, Alnylam owns or has in-licensed over 1,800
active patent cases, of which over 700 have issued or been granted
worldwide, and over 300 have issued or been granted in the U.S., Europe,
or Japan, the world’s largest pharmaceutical markets.
About Alnylam Intellectual Property (IP)
Alnylam’s IP estate includes issued, allowed, or granted fundamental
patents in many of the world’s major pharmaceutical markets that claim
the broad structural and functional properties of RNAi therapeutic
products. These include, but are not limited to:
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the Crooke Patents (U.S. Patent Nos. 5,898,031, 6,107,094, 7,432,249,
7,432,250, 7,629,321 and EP 0928290) issued in over 15 countries and
licensed exclusively from Isis Pharmaceuticals, Inc. to Alnylam for
RNAi therapeutics, which cover compositions, methods, and uses of
modified oligonucleotides, including double stranded RNAs, to
inactivate a target mRNA mediated by a double stranded RNase, such as
"RISC,” which is the cellular enzyme complex that mediates RNAi;
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the Glover ’375 patent (EP 1230375), granted in July 2005, licensed
exclusively to Alnylam from Cancer Research Technologies, Ltd., and
currently under appeal, which covers therapeutic uses of
double-stranded RNA expressed from endogenous templates or expression
vectors to mediate RNA interference in mammalian cells;
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the Kreutzer-Limmer I ’719 patent (EP 1550719), owned by Alnylam and
where the company has received a notification of ‘intent to grant’,
which covers siRNAs comprising 15-21 nucleotides in length stabilized
by chemical linkages;
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the Kreutzer-Limmer I ’235 patent (DE 10066235), granted in January
2008 and owned by Alnylam, which covers methods, uses, and medicaments
of siRNAs, with a length between 15 and 49 nucleotides, expressed
through a vector;
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the Kreutzer-Limmer I ’945 patent (EP 1214945) granted in June 2005,
currently under appeal, and owned by Alnylam, which covers
compositions, methods, and uses of siRNAs with a length between 15 and
49 nucleotides;
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the Kreutzer-Limmer I ’167 patent (DE 10080167) granted in October
2007, currently under appeal, and owned by Alnylam, which covers
pharmaceutical compositions and uses of siRNAs with a length between
15 and 49 nucleotides that target certain broad categories of
mammalian genes;
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the Kreutzer-Limmer II ’061 patent (EP 1352061), granted in May 2006
and owned by Alnylam, which covers therapeutic compositions, methods,
and uses of siRNA and derivatives directed toward approximately 130
disease targets;
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the Tuschl I patent (EP 1309726), granted in December 2009, and
exclusively licensed to Alnylam from the Max Planck Society, the
Massachusetts Institute of Technology, and Whitehead Institute, which
covers methods for using certain dsRNAs for RNAi;
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the Tuschl II ’704 patent (U.S. Patent No. 7,056,704) issued in June
2006 and exclusively licensed to Alnylam from the Max Planck Society,
which broadly covers methods of making siRNAs to silence any and all
disease target genes;
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the Tuschl II ’196 patent (U.S. Patent No. 7,078,196) issued in July
2006 and exclusively licensed to Alnylam from the Max Planck Society,
which broadly covers methods of making siRNAs with or without chemical
modifications;
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the Tuschl II ’044 patent (EP 1407044), granted in January 2008 and
exclusively licensed to Alnylam from the Max Planck Society, which
broadly covers compositions, methods, and uses of siRNAs;
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the Tuschl II patent (JP 4 095 895) granted in May 2008 in Japan and
exclusively licensed to Alnylam from the Max Planck Society, which
broadly covers compositions, methods, uses, and systems of siRNAs;
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the Tuschl II patent (Application No. 01820900.9) in China which
received an intent to grant in April 2009 and exclusively licensed to
Alnylam from the Max Planck Society, which broadly covers
compositions, methods, uses, and systems for siRNAs;
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the Kay & McCaffrey patent (AU patent application no. 2002326410)
granted in February 2009 in Australia and exclusively licensed to
Alnylam from Stanford University, which broadly covers methods and
composition for RNAi therapeutics including siRNAs and shRNAs; and,
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many divisional and continuing patent applications pending of the
aforementioned issued or granted patents and additional patent
applications pending, including patents and patent applications
covering inventions by Crooke, Fire & Mello (U.S. Patent No.
6,506,559), Kreutzer & Limmer, Glover, Li & Kirby, Pachuk, Tuschl,
Hannon, Giordano, and Kay & McCaffrey, amongst others.
In addition to fundamental patents, Alnylam is the exclusive licensee in
the field of RNAi therapeutics for more than 175 issued chemistry
patents owned or controlled by Isis Pharmaceuticals, Inc. broadly
covering chemical modifications, including motifs and patterns of
modifications of oligonucleotides, including RNAi therapeutics. These
patents include:
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phosphorothioate and 2’-O-methyl modifications of
oligonucleotides (Buhr, U.S. Patent No. 6,476,205);
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2’-Ribose modifications of oligonucleotides (Cook, U.S. Patent Nos.
5,670,633; 6,005,087; 6,531,584; and 7,138,517);
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chemical conjugates of oligonucleotides (Manoharan, U.S. Patent No.
6,153,737); and,
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"overhang,” "blunt-end,” and nucleotide pairing design motifs
(Woppmann et al., UK 2417727), which is owned by Alnylam.
In addition to fundamental and chemistry patents, Alnylam is also the
exclusive licensee in the field of RNAi therapeutics for certain
delivery patents, including those owned and controlled by Tekmira
Pharmaceuticals Corporation, broadly covering delivery of
oligonucleotides, including RNAi therapeutics, with liposomal
formulations. These patents include:
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formulations of oligonucleotides, including siRNAs, in cationic
liposomes (Wheeler, U.S. Patent Nos. 5,976,567 and 6,815,432; and
Semple, U.S. Patent No. 6,858,225); and,
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chemically modified siRNAs with "drug-like” properties for in vivo
delivery (Soutschek and Manoharan, U.S. patent application 10/916,185
/Allowed).
Alnylam is also contributing on a royalty-free/non-profit basis its
technology and more than 1,500 issued or pending patents from its RNAi
patent estate to the patent pool initiated by GlaxoSmithKline in 2009.
The patent pool was formed to aid in the discovery and development of
new medicines for the treatment of 16 neglected tropical diseases (NTD),
as defined by the U.S. Food and Drug Administration, in the world’s
least developed countries. In January 2010, BIO Ventures for Global
Health (BVGH) was chosen as administrator of patent pool. In this role,
BVGH will organize disease-specific meetings that identify the gaps in
expertise and intellectual property that currently exist in product
development for neglected diseases, and will help global health
researchers work with industry to fill these gaps to create medicines
for neglected diseases faster and more efficiently.
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 Alnylam Pharmaceuticals
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 Kirin. In
addition, the company is developing RNAi therapeutics for the treatment
of a wide range of disease areas, including liver cancers, TTR-mediated
amyloidosis, hypercholesterolemia, and Huntington’s disease. 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, Novartis, Biogen Idec, Roche,
Takeda, Kyowa Hakko Kirin, and Cubist. Alnylam and Isis are joint owners
of Regulus Therapeutics Inc., a company focused on the discovery,
development, and commercialization of microRNA-based therapeutics.
Founded in 2002, Alnylam maintains headquarters in Cambridge,
Massachusetts. For more information, please visit www.alnylam.com.
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 products and to successfully prosecute
and enforce its patents around the world, 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 Securities and Exchange
Commission. In addition, any forward-looking statements represent
Alnylam’s views only as of today and should not be relied upon as
representing its views as of any subsequent date. Alnylam does not
assume any obligation to update any forward-looking statements.