-Experienced alliance management team in place to advance
partnered microRNA therapeutic programs -
LA JOLLA, Calif., Feb 28, 2011 (BUSINESS WIRE) --
Regulus
Therapeutics Inc. today announced the appointment of Renee Lamb as
senior director of global alliance and strategic planning and Kevin
Steffy, Ph.D. as director of alliance and project management. Together
they will lead global alliance and strategic planning efforts at
Regulus. Ms. Lamb will be responsible for the management of the
company's key alliances and Dr. Steffy will direct specific
collaboration programs.
"Regulus believes in establishing deep and meaningful relationships with
its strategic partners," said Garry E. Menzel, Ph.D., chief operating
officer and executive vice president of finance of Regulus. "We treat
our alliances with sanofi-aventis and GlaxoSmithKline as true
collaborations rather than business transactions and the addition of
Renee and Kevin to specifically focus on delivering successful microRNA
therapeutics from these collaborations is a clear demonstration of that
commitment."
Ms. Lamb brings over twenty years of proven expertise in program and
portfolio management, regulatory, compliance, and quality at biotech
startups, including Anadys Pharmaceuticals, Biogen IDEC, and Genentech.
She has led the alliance management function for numerous global
strategic alliances, and has contributed to the approval and
commercialization of several biologics, including Rituxan, Zevalin,
Pulmozyme, and Activase. Lamb received a B.S. in Biology from Gonzaga
University in Spokane, WA and an M.S. in Computer Science from the
University of Southern California in Los Angeles, CA.
Dr. Steffy is a trained virologist with previous experience as a
director of virology at Anadys Pharmaceuticals, where he directed
discovery research and participated in the clinical development of
inhibitors of HCV. Prior to that, Dr. Steffy was the group leader in the
anti-infective research division at Abbott Laboratories, where he
participated in the discovery and pre-clinical development of inhibitors
to HIV, HCV, and Influenza. Dr. Steffy received a Ph.D. in Molecular
Biology from the University of Tennessee and a B.S. in Microbiology from
the University of Pittsburgh.
About microRNAs
The discovery of microRNA
in humans during the last decade is one of the most exciting scientific
breakthroughs in recent history. microRNAs are small RNA molecules,
typically 20 to 25 nucleotides in length, that do not encode proteins
but instead regulate gene expression. More than 700 microRNAs have been
identified in the human genome, and over one-third of all human genes
are believed to be regulated by microRNAs. A single microRNA can
regulate entire networks of genes. As such, these molecules are
considered master regulators of the human genome. microRNAs have been
shown to play an integral role in numerous biological processes,
including the immune response, cell-cycle control, metabolism, viral
replication, stem cell differentiation and human development. Most
microRNAs are conserved across multiple species, indicating the
evolutionary importance of these molecules as modulators of critical
biological pathways. Indeed, microRNA expression or function has been
shown to be significantly altered in many disease states, including
cancer, heart failure and viral infections. Targeting microRNAs with
anti-miRs, antisense oligonucleotide inhibitors of microRNAs, or
miR-mimics, double-stranded oligonucleotides to replace microRNA
function opens potential for a novel class of therapeutics and offers a
unique approach to treating disease by modulating entire biological
pathways. To learn more about microRNAs, please visit http://www.regulusrx.com/microrna/microrna-explained.php
About Regulus Therapeutics Inc.
Regulus Therapeutics is a biopharmaceutical company leading the
discovery and development of innovative new medicines targeting
microRNAs. Regulus is using a mature therapeutic platform based on
technology that has been developed over 20 years and tested in more than
5,000 humans. In addition, Regulus works with a broad network of
academic collaborators and leverages the oligonucleotide drug discovery
and development expertise of its founding companies, Alnylam
Pharmaceuticals (NASDAQ:ALNY) and Isis Pharmaceuticals (NASDAQ:ISIS).
Regulus is advancing microRNA therapeutics towards the clinic in several
key areas including hepatitis C infection, immuno-inflammatory diseases,
fibrosis, oncology, and cardiovascular/metabolic diseases. Regulus'
intellectual property estate contains both the fundamental and core
patents in the field and includes over 600 patents and more than 300
pending patent applications pertaining primarily to chemical
modifications of oligonucleotides targeting microRNAs for therapeutic
applications. In April 2008, Regulus formed a major alliance with
GlaxoSmithKline to discover and develop microRNA therapeutics for
immuno-inflammatory diseases. In February 2010, Regulus and
GlaxoSmithKline entered into a new collaboration to develop and
commercialize microRNA therapeutics targeting microRNA-122 for the
treatment of hepatitis C infection. In June 2010, Regulus and
sanofi-aventis entered into the largest-to-date strategic alliance for
the development of microRNA therapeutics. This alliance is focused
initially on fibrosis. For more information, visit http://www.regulusrx.com
Forward-Looking Statements
This press release includes forward-looking statements regarding the
future therapeutic and commercial potential of Regulus' business plans,
technologies and intellectual property related to microRNA therapeutics
being discovered and developed by Regulus. Any statement describing
Regulus' goals, expectations, financial or other projections, intentions
or beliefs is a forward-looking statement and should be considered an
at-risk statement. 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 forward-looking statements also
involve assumptions that, if they never materialize or prove correct,
could cause the 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 Regulus'
management, these statements are based only on facts and factors
currently known by Regulus. As a result, you are cautioned not to rely
on these forward-looking statements. These and other risks concerning
Regulus' programs are described in additional detail in Alnylam's annual
report on Form 10-K for the year ended December 31, 2011, and Isis'
annual report on Form 10-K for the year ended December 31, 2010 and
Isis' most recent quarterly report on Form 10-Q, which are on file with
the SEC. Copies of these and other documents are available from either
Isis or Alnylam.

SOURCE: Regulus Therapeutics
Regulus Therapeutics
Zachary Zimmerman, Ph.D., 858-202-6300
busdev@regulusrx.com
or
Russo Partners
Heidi Chokeir, Ph.D., 619-528-2217 (Media)
heidi.chokeir@russopartnersllc.com