Regulus Therapeutics Inc., Alnylam Pharmaceuticals, Inc. (Nasdaq: ALNY),
and Isis Pharmaceuticals, Inc. (Nasdaq: ISIS), announced today that the
Japan Patent Office (JPO) has notified the Max Planck Society of its
intent to grant a patent from the Tuschl III patent series (JP
Application Number 2003-532675). This patent series pertains to the
discovery of over 120 novel mammalian microRNAs, including miR-122,
which is a leading pre-clinical program at Regulus. The grant of this
first Tuschl III patent in Japan extends the scope of this patent
estate, which has already yielded patents in the U.S. (U.S. Patent No.
7,232,806) and in Australia (Australian Patent No. 2002 347 035).
The Tuschl III patent series stems from groundbreaking research
(Lagos-Quintana et al., (2001) Science 294, 853-858)
performed by Alnylam founder and Regulus scientific advisory board
member Dr. Thomas Tuschl, Associate Professor of RNA Molecular Biology
at The Rockefeller University, while at the Max Planck Society. The
Tuschl III patent series is exclusively held by Regulus for microRNA
therapeutics through license agreements amongst Max Planck, Alnylam, and
Isis.
"Regulus is advancing a whole new frontier of pharmaceutical research
through the discovery of microRNA therapeutics, which have the potential
to affect broad disease pathways as opposed to single gene targets,”
said Kleanthis G. Xanthopoulos, Ph.D., President and Chief Executive
Officer of Regulus Therapeutics. "Through our partnerships with Alnylam,
Isis, and our relationships with leading academic institutions such as
the Max Planck, we have built a dominant intellectual property estate
for the development of microRNA therapeutics. This is first in the
Tuschl III series to grant in Japan, and we expect more to come from
this important and early patent series.”
"We are pleased with the continued recognition of the pioneering
contributions of Professor Tuschl’s work performed at the Max Planck,”
said Dr. Joern Erselius, Managing Director, Max Planck-Innovation GmbH.
"The Tuschl III patent series describes an important set of discoveries
for the advancement of microRNA therapeutics. With Regulus, we have an
ideal partner for the development of this seminal research into a
promising new approach for medicine.”
The newly granted claims of the Tuschl III patent cover miR-122, a
liver-specific microRNA that has subsequently been shown to facilitate
replication of hepatitis C virus (HCV) infection. The claims cover
single-stranded and double-stranded antisense compounds complementary to
mir-122, as well as precursors and analogs of mir-122.
Regulus is advancing microRNA therapeutics targeting miR-122, among
others. Pre-clinical studies suggest that miR-122 is essential for the
replication of HCV (Jopling et al. (2005) Science 309,
1577-81) and that creating an inhibitor to miR-122 may define a novel
therapeutic strategy for the treatment of HCV infection.
About microRNAs
microRNAs are small, non-coding RNAs that regulate a large number of
human genes; there are more than 700 microRNAs in the human genome that
play a role in controlling expression of over one-third of all human
genes. Abnormal expression and genetic mutation of microRNAs have been
linked to numerous diseases including cancer, cardiovascular disease,
metabolic disease, autoimmunity, and viral infection, among others. In
2005, Alnylam scientists and collaborators at The Rockefeller University
were the first to describe antagomirs, which are part of a larger class
of microRNA inhibitors known as anti-miRs (Krutzfeldt et al.,
(2005) Nature 438, 685-689). Anti-miRs were created to
selectively inhibit microRNAs expressed in a broad range of tissues and
to have pharmacological properties required for microRNA-based
therapeutics. This research has created new drug discovery strategies
focused on antagonizing microRNAs.
About Regulus Therapeutics Inc.
Regulus Therapeutics Inc. is a biopharmaceutical company aiming to
discover, develop, and commercialize microRNA-based therapeutics.
Regulus aspires to translate one of the most important new discoveries
in biology into a novel approach for innovative medicines and to build
the leading microRNA company. Regulus was established by Alnylam
Pharmaceuticals (Nasdaq: ALNY) and ISIS Pharmaceuticals (Nasdaq: ISIS)
in September of 2007, and benefits substantially from their RNA
therapeutic drug discovery expertise, unique and established
oligonucleotide-based technologies, and a broad and dominant
intellectual property estate specific to microRNA-based therapeutics.
Regulus’ patent estate includes over 600 patents and more than 300
pending patent applications pertaining primarily to chemical
modifications of oligonucleotides targeting microRNA for therapeutic
applications. In addition, through its numerous collaborations with
academic researchers, Regulus continues to expand its knowledge on the
biological role of therapeutically relevant microRNAs. In April 2008,
Regulus formed a major alliance with GlaxoSmithKline to explore microRNA
therapeutics for immuno-inflammatory diseases. Regulus is headquartered
in Carlsbad, California. For more information, visit www.regulusrx.com.
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
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. To reflect its outlook for key
scientific, clinical, and business initiatives, Alnylam established "RNAi
2010” in January 2008 which includes the company’s plan to
significantly expand the scope of delivery solutions for RNAi
therapeutics, have four or more programs in clinical development, and to
form four or more new major business collaborations, all by the end of
2010. 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.
About Isis Pharmaceuticals, Inc.
Isis is exploiting its expertise in RNA to discover and develop novel
drugs for its product pipeline and for its partners. The Company has
successfully commercialized the world’s first antisense drug and has 19
drugs in development. Isis’ drug development programs are focused on
treating cardiovascular, metabolic and severe neurodegenerative diseases
and cancer. Isis’ partners are developing antisense drugs invented by
Isis to treat a wide variety of diseases. Isis and Alnylam
Pharmaceuticals are joint owners of Regulus Therapeutics Inc., a company
focused on the discovery, development and commercialization of microRNA
therapeutics. Isis also has made significant innovations beyond human
therapeutics resulting in products that other companies, including
Abbott, are commercializing. As an innovator in RNA-based drug discovery
and development, Isis is the owner or exclusive licensee of over 1,600
issued patents worldwide. Additional information about Isis is available
at www.isispharm.com.
Forward-Looking Statements
This press release includes forward-looking statements regarding the
future therapeutic and commercial potential of Regulus’, Alnylam’s, and
Isis’ business plans, technologies and intellectual property related to
microRNA therapeutics being discovered and developed by Regulus. Any
statement describing Regulus’, Alnylam’s, and Isis’ goals, expectations,
financial or other projections, intentions or beliefs is a
forward-looking statement and should be considered an at-risk statement,
including those statements that are described as such parties’ goals.
Such statements are subject to certain risks and uncertainties,
particularly those inherent in the process of discovering, developing
and commercializing drugs that are safe and effective for use as human
therapeutics, and in the endeavor of building a business around such
products. Such parties’ forward-looking statements also involve
assumptions that, if they never materialize or prove correct, could
cause their results to differ materially from those expressed or implied
by such forward-looking statements. Although these forward-looking
statements reflect the good faith judgment of the management of each
such party, these statements are based only on facts and factors
currently known by Regulus’, Alnylam’s, and Isis’ as the case may be. As
a result, you are cautioned not to rely on these forward-looking
statements. These and other risks concerning Regulus’, Alnylam’s, and
Isis’ programs are described in additional detail in Alnylam’s and Isis’
annual reports on Form 10-K for the year ended December 31, 2008, and
their most recent quarterly reports on Form 10-Q which are on file with
the SEC. Copies of these and other documents are available from Alnylam
or Isis.