SGX Pharmaceuticals BCR-ABL Program to be Presented at the American Society of Hematology 49th Annual Meeting and Exposition
December 06 2007 - 6:00AM
PR Newswire (US)
SAN DIEGO, Dec. 6 /PRNewswire-FirstCall/ -- SGX Pharmaceuticals,
Inc. (NASDAQ:SGXP) announced today details of two presentations
from the Company's BCR-ABL program for the treatment of chronic
myelogenous leukemia (CML) at the upcoming American Society of
Hematology's 49th Annual Meeting and Exposition. The conference is
being held December 8th - 11th, 2007 in Atlanta, Georgia. The
schedule for these sessions, together with the abstract
information, is listed below: Date: Saturday, December 8, 2007 from
5:30pm - 7:30pm EST Session Type: Poster Session, Board #172-I
Abstract: #1018 Title: "Co-Crystal Structures of 7-Azaindole
Inhibitors of Wild-Type and T315I Imatinib-Resistant Mutant Forms
of the BCR-ABL Tyrosine Kinase." Description: This poster
presentation describes how the SGX393 chemical family of BCR-ABL
inhibitors discovered by SGX can provide potent, selective
inhibition of both wild type and major drug resistant mutant forms
of BCR-ABL including T315I. The poster discusses the impact of
seven BCR-ABL mutations on the co-crystal structures of the SGX393
family of inhibitors, including the challenging T315I, G250E and
F317L mutations. SGX393 represents an illustrative example of how
the integrated SGX FAST fragment-based, structure-guided drug
discovery platform can be used to generate high-quality, low
molecular weight inhibitors of oncology targets. Date: Monday,
December 10, 2007 from 1:30pm - 3:00pm EST Session Type: Oral
Session Abstract: #535 Title: "SGX70393 Inhibits BCR-ABL &
T315I In Vitro and In Vivo and Completely Suppresses Resistance
When Combined with Nilotinib or Dasatinib." Description: An oral
presentation, coauthored with collaborators at the Oregon Health
& Science University Cancer Institute, describes a proof of
principle study demonstrating the potential of combination targeted
therapy for CML. SGX393 (also known as SGX70393) is a potent,
selective orally-bioavailable inhibitor of both wild type and major
drug resistant mutant forms of BCR-ABL, including the most
challenging T315I mutation. "These two ASH presentations explain
how SGX is using its drug discovery platform to discover and
optimize potent, selective and orally-bioavailable inhibitors of
important oncology drug discovery targets," said Stephen Burley,
Chief Scientific Officer of SGX Pharmaceuticals. "Moreover, the
results obtained with our collaborators at the Oregon Health &
Science University Cancer Institute demonstrate the potential of
targeted combination therapy for CML. A number of influential
thought leaders believe that effective management of
newly-diagnosed CML will depend on long-term treatment with
multiple agents possessing non-overlapping resistance profiles."
About the SGX BCR-ABL Program SGX393 is an internally developed,
orally-bioavailable, small molecule inhibitor of the abnormal
BCR-ABL tyrosine kinase, which results from a characteristic
chromosome abnormality (also known as the Philadelphia chromosome)
that causes chronic myelogenous leukemia or CML, a cancer of the
bone marrow. SGX393 has shown both potent in vitro blockade of the
activity of BCR-ABL and in vivo activity against human leukemic
cells that depend on BCR-ABL for their uncontrolled growth and
proliferation. In addition, SGX393 has shown potent activity
against a broad spectrum of mutant forms of BCR-ABL that render
this cancer target resistant to imatinib (Gleevec (R)), the current
standard of care for CML. One of the key drug resistant forms of
BCR-ABL inhibited by SGX393 is the T315I mutation, which is also
resistant to the two second-generation BCR-ABL inhibitors,
nilotinib (Tasigna (R)) and dasatinib (Sprycel (R)). In addition,
SGX is engaged in a strategic collaboration with Novartis that aims
to discover and develop next generation BCR-ABL inhibitors for
treatment of newly-diagnosed CML patients. About SGX
Pharmaceuticals SGX Pharmaceuticals is a biotechnology company
focused on the discovery, development and commercialization of
innovative cancer therapeutics. The SGX oncology pipeline includes
drug candidates from its FAST(TM) drug discovery platform, such as
next generation BCR-ABL inhibitors being developed by SGX and in
partnership with Novartis and cMET tyrosine kinase inhibitors,
including SGX523, and JAK2 inhibitors. More information on the
pipeline and drug discovery platform can be found at
http://www.sgxpharma.com/ and in the Company's various filings with
the Securities and Exchange Commission. Forward-looking Statements
Statements in this press release that are not strictly historical
in nature are forward-looking statements. These statements include,
but are not limited to, research and development programs, the
potential of SGX's BCR-ABL inhibitors as treatments for chronic
myelogenous leukemia and the ability to discover, develop and
commercialize cancer therapeutics. These statements are only
predictions based on current information and expectations and
involve a number of risks and uncertainties. Actual events or
results may differ materially from those projected in any of such
statements due to various factors, including the risks and
uncertainties inherent in drug discovery, development and
commercialization. The results of early preclinical studies or
clinical trials may not be predictive of future results, and the
Company cannot provide any assurances that any of its compounds or
development candidates will have favorable results in preclinical
studies or future clinical trials. For a discussion of these and
other factors, please refer to the risk factors described in the
Company's annual report on Form 10-K for the year ended December
31, 2006, the Company's quarterly report on Form 10-Q for the three
and nine months ended September 30, 2007, as well as other filings
with the Securities and Exchange Commission. You are cautioned not
to place undue reliance on these forward-looking statements, which
speak only as of the date hereof. This caution is made under the
safe harbor provisions of the Private Securities Litigation Reform
Act of 1995. All forward-looking statements are qualified in their
entirety by this cautionary statement and SGX undertakes no
obligation to revise or update this press release to reflect events
or circumstances after the date hereof. DATASOURCE: SGX
Pharmaceuticals, Inc. CONTACT: Todd Myers, Chief Financial Officer
of SGX Pharmaceuticals, +1-858-558-4850; or Jason Spark, Media
& Investor Relations of Porter Novelli Life Sciences,
+1-619-849-6005, for SGX Pharmaceuticals, Inc. Web site:
http://www.sgxpharma.com/
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