Aptose Submits Formal Response to Clinical Hold for APTO-253
12 9월 2016 - 9:00PM
Aptose Biosciences Inc. (NASDAQ:APTO) (TSX:APS), a clinical-stage
company developing new therapeutics and molecular diagnostics that
target the underlying mechanisms of cancer, announced today that it
has submitted a formal response to the U.S. Food and Drug
Administration (FDA) regarding the previously announced clinical
hold of Aptose’s Phase 1b clinical trial of APTO-253 in patients
with hematologic cancers. Aptose provided responses to all of
the questions cited in the clinical hold letter issued by the FDA.
“This submission represents months of
disciplined labor to resolve a manufacturing matter related to
APTO-253 that arose during our Phase 1b Trial in patients with AML
and high-risk MDS,” commented Dr. William G. Rice, Chairman,
President and Chief Executive Officer. “Although the FDA will make
the ultimate decision whether our clinical trial may resume, all of
their questions have been addressed.”
During a Phase 1b clinical trial with APTO-253,
a clinical site experienced stoppage of the infusion pump during an
IV infusion caused by back pressure as a result of clogging of the
in-line filter. The Company determined the root cause was a
chemistry-based issue with the molecule, and the Company is now
working with a drug product that does not cause filter clogging or
pump stoppage during mock infusion studies performed to confirm the
acceptability of the updated product through the clinical infusion
procedures. Such improvements to the APTO-253 manufacturing process
required to address the filter clogging event will be incorporated
into a Chemistry, Manufacturing and Control (CMC) amendment to our
Investigational New Drug application.
About Aptose
Aptose Biosciences is a clinical-stage
biotechnology company developing personalized therapies to address
unmet medical needs in oncology, with a particular focus on
hematologic malignancies. Aptose is advancing new therapeutics
focused on well validated and novel drug targets on the leading
edge of cancer research, coupled with validated biomarkers to
identify the optimal patient population for our products. The
company's small molecule cancer therapeutics pipeline includes
products designed for potent single agent activity and to enhance
the efficacy of existing anti-cancer therapies without overlapping
toxicities. Aptose Biosciences Inc. is listed on NASDAQ under the
symbol APTO and on the TSX under the symbol APS. For further
information, please visit www.aptose.com.
Forward Looking Statements
This press release contains forward-looking
statements within the meaning of Canadian and U.S. securities laws.
Such statements include, but are not limited to, statements
relating to the return of APTO-253 to the clinic and the process to
have the clinical hold lifted by the FDA and statements relating to
the Company’s plans, objectives, expectations and intentions and
other statements including words such as “continue”, “expect”,
“intend”, “will”, “should”, “would”, “may”, and other similar
expressions. Such statements reflect our current views with respect
to future events and are subject to risks and uncertainties and are
necessarily based upon a number of estimates and assumptions that,
while considered reasonable by us are inherently subject to
significant business, economic, competitive, political and social
uncertainties and contingencies. Many factors could cause our
actual results, performance or achievements to be materially
different from any future results, performance or achievements
described in this press release. Such factors could include, among
others: our ability to obtain the capital required for research and
operations; the inherent risks in early stage drug 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; uncertainty in the length of the clinical hold
and the conditions the FDA may impose to lift it; inability of new
manufacturers to produce acceptable batches of GMP in sufficient
quantities; unexpected manufacturing defects; and other risks
detailed from time-to-time in our ongoing quarterly filings, annual
information forms, annual reports and annual filings with Canadian
securities regulators and the United States Securities and Exchange
Commission.
Should one or more of these risks or
uncertainties materialize, or should the assumptions set out in the
section entitled "Risk Factors" in our filings with Canadian
securities regulators and the United States Securities and Exchange
Commission underlying those forward-looking statements prove
incorrect, actual results may vary materially from those described
herein. These forward-looking statements are made as of the date of
this press release and we do not intend, and do not assume any
obligation, to update these forward-looking statements, except as
required by law. We cannot assure you that such statements will
prove to be accurate as actual results and future events could
differ materially from those anticipated in such statements.
Investors are cautioned that forward-looking statements are not
guarantees of future performance and accordingly investors are
cautioned not to put undue reliance on forward-looking statements
due to the inherent uncertainty therein.
For further information, please contact:
Aptose Biosciences
Greg Chow, CFO
647-479-9825
gchow@aptose.com
SMP Communications, Inc.
Susan Pietropaolo
845-638-6290
susan@smpcommunications.com
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