Sirna Therapeutics Announces Its Scientific Advisory Board
March 14 2006 - 8:37AM
PR Newswire (US)
Eleven Renowned Researchers to Guide Sirna's Advancing Therapeutic
Pipeline SAN FRANCISCO, March 14 /PRNewswire-FirstCall/ -- Sirna
Therapeutics (NASDAQ:RNAI), a leading RNAi therapeutics company,
has announced its Scientific Advisory Board (SAB). Joining Keith
Yamamoto, Ph.D., Executive Vice Dean for Research at the University
of California, San Francisco School of Medicine and Chairman of the
Sirna SAB are ten world-renowned scientists who bring expertise in
key areas that will be invaluable in transitioning Sirna's pipeline
programs from discovery to the clinic. Chaired by Dr. Yamamoto, the
members of the Sirna Scientific Advisory Board are: * Jeffrey A.
Bluestone, Ph.D., A.W. and Mary Margaret Clausen Distinguished
Professor of Medicine, Pathology, Microbiology & Immunology at
the University of California, San Francisco (UCSF). He is the
Director of the UCSF Diabetes Center, the Immune Tolerance Network,
and the Juvenile Diabetes Research Foundation Collaborative Center
for Cellular Therapy. Dr. Bluestone is an expert in diabetes and
immunology * Beverly Davidson, Ph.D., Roy J. Carver Professor in
Internal Medicine and Professor in Neurology, Physiology &
Biophysics at the University of Iowa. Dr. Davidson is an expert in
neurodegenerative diseases and the therapeutic use of siRNAs *
Donald Ganem, M.D., Professor, Microbiology/Immunology and Medicine
at the University of California, San Francisco and a Howard Hughes
Medical Institute Investigator. Dr. Ganem is an expert in viral
diseases * Joe W. Gray, Ph.D., Associate Laboratory Director for
Life and Environmental Sciences at the Lawrence Berkeley National
Laboratory (LBNL) and the Director of the LBNL Life Sciences
Division. Dr. Gray also is Adjunct Professor of Laboratory Medicine
at the University of California, San Francisco (UCSF). Dr. Gray is
an expert in neoplastic diseases, breast and ovarian cancer in
particular * Stanley M. Lemon, M.D., Director, Institute for Human
Infections and Immunity Professor, Departments of Microbiology
& Immunology and Internal MedicineUniversity of Texas Medical
Branch. Dr. Lemon is an expert in chronic hepatitis C and innate
immunity * Richard Locksley, M.D., Herbert and Marion Sandler
Distinguished Professorship in Asthma Research; Professor of
Medicine and Microbiology/Immunology, at the University of
California, San Francisco and a Howard Hughes Medical Institute
Investigator. Dr. Locksley is an expert in infectious disease and
immunology * Jerrold M. Olefsky, M.D., Professor of Medicine and
Co-Chair, Division of Endocrinology & Metabolism at the
University of California, San Diego. Dr. Olefsky is an expert in
type II diabetes and metabolic diseases * David W. Russell, Ph.D.,
Eugene McDermott Distinguished Chair in Molecular Genetics at the
University of Texas Southwestern. Dr. Russell is an expert in lipid
metabolism and endocrine disorders * Xiaodong Wang, Ph.D., George
L. MacGregor Distinguished Chair in Biomedical Science at the
University of Texas Southwestern Medical School and a Howard Hughes
Medical Institute Investigator. Dr. Wang is an expert in apoptosis
and the RNA interference mechanism * James A. Wells, Ph.D., Harry
Wm. and Diana V. Hind Professorship in Pharmaceutical Sciences and
Professor of Pharmaceutical Chemistry and Cellular and Molecular
Pharmacology at the University of California, San Francisco. Dr.
Wells is an expert in molecular recognitions, the protein design
and site-directed design of small molecule ligands "We are very
pleased to bring together these key thought leaders to establish
the Sirna Scientific Advisory Board," stated Barry Polisky, Sirna
Senior Vice President and Chief Scientific Officer. "Their deep
insight into the etiology of important human diseases will be
instrumental in advancing our therapeutic programs to the clinic.
Further, the interest and direct participation of these world class
scientists on our SAB reflects the progress we're making in the
development of RNAi-based therapeutics." "During the past year,
Sirna has made important advances in the development of RNAi-based
therapeutics," said Dr. Yamamoto. "The completion of the Phase I
clinical trial for Sirna-027 in age-related macular degeneration
and the demonstration of systemic efficacy in non-human primates
leading to the selection of a clinical candidate in hepatitis C has
established Sirna as a leading siRNA therapeutics company. I expect
that this exceptional SAB will make a significant contribution to
Sirna's therapeutic programs and their ultimate success in the
clinic." About Sirna Therapeutics Sirna Therapeutics is a
clinical-stage biotechnology company developing RNAi-based
therapies for serious diseases and conditions, including
age-related macular degeneration (AMD), hepatitis B and C,
dermatology, asthma, Huntington's disease, diabetes and oncology.
Sirna Therapeutics has presented interim Phase 1 clinical trial
data for its most advanced compound, Sirna-027, a chemically
optimized siRNA targeting the clinically validated vascular
endothelial growth factor pathway to treat AMD. Sirna-027, which
has been partnered with Allergan, Inc., has demonstrated that it is
safe and well tolerated with 25 of 26 patients showing visual
acuity stabilization and 23% of those patients experiencing
clinically significant improvement in visual acuity eight weeks
after a single injection. In addition, Sirna recently announced
that it has selected Sirna-034, a systemically delivered, optimized
siRNA compound, as its candidate for advancement to human clinical
testing against Hepatitis C virus. Sirna has a leading intellectual
property portfolio in RNAi with 50 issued patents and over 250
pending applications worldwide. More information on Sirna
Therapeutics is available on the Company's web site at
http://www.sirna.com/. Safe Harbor Statement Statements in this
press release which are not strictly historical are
"forward-looking" statements which should be considered as subject
to many risks and uncertainties. For example, most drug candidates
do not become approved drugs. The development of Sirna-027 and
Sirna-034 as well as Sirna's other programs are still at a
relatively early stage and subject to significant risks and
unknowns. Moreover, Sirna's ability to develop products and operate
as a going concern requires significant cash to fund its operating
programs. Additional risks and uncertainties include Sirna's early
stage of development and short operating history, Sirna's history
and expectation of losses and need to raise capital, the rate at
which Sirna uses cash, the timing of receipt of development
milestone payments from collaborating partners, Sirna's need to
obtain clinical validation and regulatory approval for products,
Sirna's need to obtain and protect intellectual property, risk of
third-party patent infringement claims, Sirna's need to attract and
retain qualified personnel, Sirna's need to engage collaborators,
availability of materials for product manufacturing, the highly
competitive nature of the pharmaceutical market, the limited
trading volume and history of volatility of Sirna's common stock,
Sirna's concentration of stock ownership, and risks from relocating
Sirna headquarters. These and additional risk factors are
identified in Sirna's Securities and Exchange Commission filings,
including the Forms 10-K and 10-Q and in other SEC filings. Sirna
undertakes no obligation to revise or update any forward-looking
statements in order to reflect events or circumstances that may
arise after the date of this release. Contacts: Rebecca Galler
Robison, Senior Director, Corporate Strategy of Sirna Therapeutics,
Inc., 303-449-6500 Alan Zachary, McKinney Chicago, 312-944-6784
x316 DATASOURCE: Sirna Therapeutics, Inc. CONTACT: Rebecca Galler
Robison, Senior Director, Corporate Strategy of Sirna Therapeutics,
Inc., +1-303-449-6500; or Alan Zachary of McKinney Chicago,
+1-312-944-6784, ext. 316, for Sirna Therapeutics, Inc. Web site:
http://www.sirna.com/
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