20.03.2008 12:00:00
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Alnylam Grants Shanghai GenePharma License to Kreutzer-Limmer Patents for the RNA Interference (RNAi) Research Products Market
Alnylam Pharmaceuticals, Inc. (Nasdaq: ALNY), a leading RNAi
therapeutics company, and Shanghai GenePharma Co., Ltd, a leading siRNA
supplier in China, announced today that Alnylam has granted Shanghai
GenePharma a non-exclusive world-wide license to manufacture and provide
RNAi research products and services under the Kreutzer-Limmer patent
family. This patent family, owned exclusively by Alnylam, covers
fundamental aspects of the structure and uses of RNAi products including
their use to mediate RNAi in mammalian cells and of RNAi-related
mechanisms.
"The Kreutzer-Limmer patent family is one of
the critical components of fundamental intellectual property in the
field of RNAi, and we are pleased to grant Shanghai GenePharma a license
to manufacture and provide siRNA reagents to its industry and academic
customers around the world for research purposes,”
said Jason Rhodes, Vice President of Business Development at Alnylam. "Providing
this license to Shanghai GenePharma represents our first business
transaction in China, which is regarded as having one of the fastest
growing life science markets in the world. With more than 16 license
agreements with global research product suppliers, we believe the vast
majority of industrial sales of RNAi products for research purposes are
currently being made under a license from Alnylam.” "This agreement with Alnylam, a leader in the
field of RNAi, reinforces our ability to become a leading global
supplier of RNAi reagent products to the pharmaceutical and research
community in China and worldwide,” said Peter
Zhang, Ph.D., Chairman and Chief Executive Officer of Shanghai
GenePharma. "Access to the Kreutzer-Limmer
patent estate allows us to augment our RNAi products, thereby
strengthening our position in the life sciences marketplace.”
Alnylam’s intellectual property estate
includes certain fundamental patents and patent applications, including
the Kreutzer-Limmer I and II patents, which claim the broad structural
and functional properties of synthetic RNAi products.
About RNA Interference (RNAi)
RNAi 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, and 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. RNAi therapeutics target the cause of diseases by
potently silencing specific messenger RNAs (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. In addition, the company is developing
RNAi therapeutics for the treatment of a wide range of disease areas,
including hypercholesterolemia, liver cancers, 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, and Roche. To reflect its outlook for
key scientific, clinical, and business initiatives, Alnylam has
established "RNAi 2010”
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 is a joint owner of Regulus Therapeutics LLC, a joint
venture focused on the discovery, development, and commercialization of
microRNA therapeutics. Founded in 2002, Alnylam maintains headquarters
in Cambridge, Massachusetts. For more information, visit www.alnylam.com.
About Shanghai GenePharma
Shanghai GenePharma Co., Ltd is specialized in developing, manufacturing
and supplying RNA synthesis monomers, modified RNA monomers, siRNA
oligos, miRNA oligos, etc. Currently it is expanding quickly into large
scale siRNA synthesis. At the same time, Shanghai GenePharma is very
active in developing new chemically modified siRNA synthesis
technologies, miRNA purification, detection technologies, and it started
to supply comprehensive RNAi related services to academic and industrial
customers. Founded in 2003, Shanghai GenePharma is headquartered in
Shanghai, China, and serves thousands of research and industry customers
worldwide through its global network of operations. For more
information, visit www.genepharma.com.
Alnylam Forward-Looking Statements
Various statements in this release concerning Alnylam’s
future expectations, plans, and prospects, including its views with
respect to the importance of its intellectual property rights,
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 risks related to: Alnylam’s
approach to discover and develop novel drugs, which is unproven and may
never lead to marketable products; Alnylam’s
ability to fund and the results of further pre-clinical and clinical
trials; obtaining, maintaining and protecting intellectual property
utilized by its products; Alnylam’s ability
to enforce its patents against infringers and to defend its patent
portfolio against challenges from third parties; Alnylam’s
ability to obtain additional funding to support its business activities;
Alnylam’s dependence on third parties for
development, manufacture, marketing, sales, and distribution of
products; the successful development of Alnylam’s
product candidates, all of which are in early stages of development;
obtaining regulatory approval for products; competition from others
using technology similar to Alnylam’s and
others developing products for similar uses; Alnylam’s
dependence on collaborators; and its short operating history; as well as
those risks more fully discussed in the "Risk
Factors” section of our most recent report on
Form 10-K 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.
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