Aptose Biosciences to Present CG’806 Data at AACR Hematologic Malignancies Meeting
19 Abril 2017 - 7:30AM
Aptose Biosciences Inc. (NASDAQ:APTO) (TSX:APS), a clinical-stage
company developing highly differentiated therapeutics that target
the underlying mechanisms of cancer, today announced that
preclinical data for its pan-FLT3/BTK inhibitor CG’806 will be
presented in two separate posters at the 2017 American Association
for Cancer Research (AACR) Conference Hematologic Malignancies:
Translating Discoveries to Novel Therapies, being held May 6-9 in
Boston, MA.
Aptose is developing CG’806, a first-in-class
pan-FLT3/BTK inhibitor, for acute myeloid leukemia (AML) and other
hematologic malignancies. CG’806 is a highly potent inhibitor of
the wild type and mutant forms of FLT3 (including internal tandem
duplication, or ITD, and mutations of the receptor tyrosine kinase
domain and the gatekeeper region), eliminates AML tumors in the
absence of toxicity in murine xenograft models, and represents a
potential best-in-class therapeutic for patients with FLT3-driven
AML. In addition, CG’806 is a reversible, non-covalent, inhibitor
of the wild type and mutant forms of the BTK enzymes. The spectrum
of activity against specific clusters of kinase enzymes supports
the development of CG’806 for AML, certain B cell malignancies and
other hematologic malignancies.
Two separate presentations are planned for
CG’806. Aptose scientists, with researchers from the Knight Cancer
Institute at Oregon Health & Science University (OHSU), will
present data related to the potency of CG’806 against various
hematologic malignancy cell lines and patient bone marrow
specimens. In a separate presentation, Aptose scientists, with
researchers from the MD Anderson Cancer Center, will present data
demonstrating CG’806’s potent activity against AML cells harboring
specific wild type or mutant forms of FLT3.
Abstract Details
- Title: “CG’806, a first-in-class FLT3/BTK inhibitor, exhibits
potent activity against AML patient samples with mutant or
wild-type FLT3, as well as other hematologic malignancy
subtypes”
- Presenter: Stephen E. Kurtz, Ph.D, Oregon Health & Science
University, Portland, OR
- Date/Time: May 7, 2017 / 1:00 p.m. ET – 3:00 p.m. ET
- Location: Harbor 1/2, Westin Boston Waterfront, Boston, MA
- Session: Poster Session
Abstract Details
- Title: “CG’806, a first-in-class FLT3/BTK inhibitor, exerts
superior potency against AML cells harboring ITD, TKD and
gatekeeper mutated FLT3 or wild-type FLT3”
- Presenter: Weiguo Zhang, M.D., Ph.D, UT MD Anderson Cancer
Center, Houston, TX
- Date/Time: May 7, 2017 / 1:00 p.m. ET – 3:00 p.m. ET
- Location: Harbor 1/2, Westin Boston Waterfront, Boston, MA
- Session: Poster Session
About CG’806
CG’806 is a once daily, oral, first-in-class
pan-FLT3/BTK inhibitor. This small molecule demonstrates potent
inhibition of mutant forms of FLT3 (including internal tandem
duplication, or ITD, and mutations of the receptor tyrosine kinase
domain and gatekeeper region), eliminates AML tumors in the absence
of toxicity in murine xenograft models, and represents a potential
best-in-class therapeutic for patients with FLT3-driven AML.
Likewise, CG’806 demonstrates potent, non-covalent inhibition of
the Cys481Ser mutant of the BTK enzyme, as well as other oncogenic
kinases operative in B cell malignancies, suggesting the CG’806 may
be developed for CLL and MCL patients that are
resistant/refractory/intolerant to covalent BTK inhibitors.
About Aptose
Aptose Biosciences is a clinical-stage
biotechnology company committed to developing personalized
therapies addressing unmet medical needs in oncology. Aptose is
advancing new therapeutics focused on novel cellular targets on the
leading edge of cancer. The company's small molecule cancer
therapeutics pipeline includes products designed to provide single
agent efficacy and to enhance the efficacy of other anti-cancer
therapies and regimens without overlapping toxicities. For further
information, please visit www.aptose.com.
Forward Looking Statements
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considered reasonable by us are inherently subject to significant
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performance or achievements to be materially different from any
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obtain the capital required for research and operations and to
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development including demonstrating efficacy; development time/cost
and the regulatory approval process; the progress of our clinical
trials; our ability to find and enter into agreements with
potential partners; our ability to attract and retain key
personnel; changing market conditions; inability of new
manufacturers to produce acceptable batches of GMP in sufficient
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Should one or more of these risks or
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For further information, please contact:
Aptose Biosciences
Greg Chow, CFO
647-479-9828
gchow@aptose.com
SMP Communications
Susan Pietropaolo
201-923-2049
susan@smpcommunications.com
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