Release Details
Regulus, Alnylam, and Isis Announce First microRNA Patent Grant in Japan from Tuschl III Patent Series
– Tuschl III Patent Exclusively Licensed from Max Planck –
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.
“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
“We are pleased with the continued recognition of the pioneering
contributions of Professor Tuschl’s work performed at the Max Planck,”
said Dr.
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
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
About
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.
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
Source:
Regulus Therapeutics
Garry E. Menzel, Ph.D., 760-268-6811
or
Media
Russo
Partners
Heidi Chokeir, Ph.D., 619-528-2217
or
Alnylam
Pharmaceuticals
Investors
Cynthia Clayton,
617-551-8207
or
Media
Yates Public Relations
Kathryn
Morris, 845-635-9828
or
Isis Pharmaceuticals
Investors
Kristina
Lemonidis, 760-603-2490
or
Media
Amy Blackley,
Ph.D., 760-603-2772