SAN DIEGO and
TORONTO, Nov. 4, 2014 /PRNewswire/ - Aptose Biosciences
Inc. (NASDAQ: APTO, TSX: APS) ("Aptose" or the "Company") today
reported financial results for the four months ended September 30, 2014 and provided a corporate
update. Unless specified otherwise, all amounts are in Canadian
dollars.
Effective July 15,
2014 the Company changed its fiscal year end from
May 31 to December 31. As a
result of that change, the current interim period being reported is
for the four months ended September 30,
2014, while the prior year comparative period is for the
three months ended August 31, 2013
and therefore not directly comparable to the current four-month
period. The current fiscal year will be from June 1, 2014 to December
31, 2014.
The net loss for the four months ending
September 30, 2014 was $4.2 million, or ($0.36) per share, compared with a net loss of
$1.1 million, or ($0.31) per share, for the three months ended
August 31, 2013. Total cash and cash
equivalents and short term investments as of September 30, 2014 totaled $33.1 million.
"The four-month period ended September 30, 2014 has been marked by significant
corporate achievement," said William G.
Rice, Ph.D., Chairman, President and Chief Executive
Officer. "Our listing on the NASDAQ Exchange is a major milestone
for the Company and caps off a year of solid execution under a new
leadership team. We are now well-positioned to advance our
lead program APTO-253 into later stage clinical development."
Corporate Highlights
- On September 2, 2014 the Company
announced a name change to Aptose Biosciences Inc. Aptose
reflects the Company's focus as an oncology research and
development organization advancing new therapeutics and molecular
diagnostics that are based on insights into the genetic profiles of
certain cancers and patient populations.
- On September 8, 2014 Aptose
announced that Stephen B. Howell,
M.D. would act in the capacity of Chief Medical Officer. Dr.
Howell is a renowned medical oncologist and leader in the
development of novel drugs and drug delivery systems for the
treatment of cancer and in the discovery of the molecular and
genetic mechanisms underlying drug resistance. Dr. Howell joined
the Aptose team as a medical consultant to provide expert clinical
guidance.
- During the four months ended September
30, 2014 Aptose received cash proceeds of $6.6 million related to warrant
exercises. This additional capital further strengthened the
balance sheet and demonstrated strong support from the Company's
investor base.
- Subsequent to September 30, 2014,
on October 23, 2014 the Company
announced that its common shares began trading on the NASDAQ
Capital Market under the symbol "APTO". Aptose will continue
to trade on the Toronto Stock Exchange under the symbol "APS".
APTO-253 Update
Phase 1b Trial
- On July 28, 2014 Aptose announced
that the U.S. Food and Drug Administration (FDA) had completed its
review and cleared the Investigational New Drug (IND) application
of APTO-253 for the treatment of hematologic malignancies,
including acute myeloid leukemia (AML), high-risk myelodysplastic
syndromes (MDS), lymphomas and multiple myeloma. Clearance of
the IND allows the Company to initiate a Phase 1b, multi-center,
open-label, clinical study of APTO-253 in patients with relapsed or
refractory hematologic malignancies. The Phase 1b trial will
evaluate safety, tolerability, pharmacokinetics, pharmacodynamic
responses and efficacy of APTO-253 as a single agent. The
trial is expected to enroll 45-60 patients as part of a
dose-escalation program and two separate disease-specific
single-agent expansion cohorts.
- The study will include two separate arms: one group of up to 15
patients dedicated to AML only and high-risk MDS and another group
of up to 15 patients for lymphomas and multiple myelomas. The
additional arm will allow a focused look at AML and high-risk MDS,
will allow exploration of the effect of APTO-253 on lymphomas and
myelomas, and will provide patient data on two times the
number of patients during 2015 than would have been possible with a
single arm study.
- The primary objectives of this Phase 1b trial are: (i) to
further assess safety on a new and optimized dosing schedule, and
(ii) to identify the recommended dose for APTO-253 for the upcoming
Phase 2 single-agent trials in hematologic malignancies, and in
subsequent Phase 2 combination trials.
- Aptose plans to monitor patient KLF4 and CDX2 levels upon entry
into the study, throughout the study, and during a post-treatment
period. Aptose will not exclude patients based on Krüppel-like
factor 4 (KLF4) or CDX2 status from participating in this first
study as it believes this approach may be useful in further
validating Aptose's companion diagnostic and observing potential
responses among the broader population.
- The Company anticipates dosing the first patient imminently in
the Phase 1b dose-escalation study, providing a potential update on
the dose-escalation study during the first half of 2015, completing
enrollment of the Phase 1b dose-escalation study by late-2015,
starting the expansion cohort studies for this study in 2016; and
starting Phase 2 combination studies in 2016.
Beat AML Collaboration
- On September 29, 2014 the Company
announced, along with the Knight Cancer Institute at Oregon Health
& Science University (OHSU) and The Leukemia & Lymphoma
Society (LLS), that Aptose has joined the Beat AML collaboration in
order to profile Aptose's lead investigational anticancer
therapeutic APTO-253 against primary cells from AML patient
samples. The collaboration is intended to provide further insights
into the genetic profile of patients likely to benefit from
APTO-253 therapy and to identify promising treatment combinations
that may further increase therapeutic efficacy. Beat AML is a
groundbreaking research initiative focused on accelerating the
development of new therapeutics for AML that brings together
industry and academic collaborators led by top scientists within
the Knight Cancer Institute in collaboration with the LLS.
American Society of Hematology
- Aptose will present an abstract on APTO-253 at the upcoming
56th American Society of Hematology (ASH) annual
meeting in San Francisco,
California which will be held in December 2014.
FINANCIAL RESULTS
Net loss for the four months ended September 30, 2014 was $4.2 million ($0.36
per share) compared with $1.1 million
($0.31 per share) during the three
months ended August 31, 2013. The
increase in net loss is due to the comparison of a four-month
period in the current period with a three-month period in the prior
year, in addition to increased research and development costs
associated with increased clinical activity on APTO-253 and higher
general and administrative costs associated with higher stock-based
compensation and increased corporate activities including the
Company's name change, share consolidation and NASDAQ listing.
Research and development expenses totaled
$1.3 million in the four months ended
September 30, 2014 compared to
$615 thousand during the three months
ended August 31, 2013. Research
and development costs consist of the following:
Components of research and development expenses: |
|
|
|
|
|
|
|
|
|
(amounts in 000's of Canadian
Dollars) |
|
Four months ended
September 30, 2014 |
|
Three months ended
August 31, 2013 |
|
|
|
|
|
|
|
|
|
|
Program costs |
|
$
1,272 |
|
$
578 |
Stock-based compensation |
|
37 |
|
33 |
Depreciation of equipment |
|
2 |
|
4 |
|
|
$
1,311 |
|
$
615 |
|
|
|
|
|
The increase in research and development costs in
the four months ended September 30,
2014 compared with the three months ended August 31, 2013 is due to a four-month period
compared with a three-month period in the prior year, as well as
increased costs associated with APTO-253 and research, clinical and
manufacturing activities as the Company prepares to launch a Phase
I clinical trial. In the prior year period there were minimal
research and development activities ongoing.
General and administrative expenses totaled
$3.0 million for the four months
ended September 30, 2014 compared to
$451 thousand in the three months
ended August 31, 2013. General
and administrative expenses consist of the following:
Components of general and administrative expenses: |
|
|
|
|
|
|
|
|
|
(amounts in 000's of Canadian
Dollars) |
|
Four months ended
September 30, 2014 |
|
Three months ended
August 31, 2013 |
|
|
|
|
|
|
|
|
|
|
General and administrative excluding salaries |
|
$
1,111 |
|
$
255 |
Salaries |
|
836 |
|
141 |
Stock-based compensation |
|
1,047 |
|
55 |
Depreciation of equipment |
|
6 |
|
− |
|
|
$
3,000 |
|
$
451 |
General and administrative costs excluding
salaries are higher in the four months ended September 30, 2014 due to a four-month period
compared with a three-month period ended August 31, 2013. In addition, in the current
period, the Company had higher legal and patent costs associated
with corporate activities (including the name change, share
consolidation and NASDAQ listing), as well as re-branding costs
associated with Aptose's name change and new website and higher
levels of administrative costs associated with additional
employees.
Salary costs have increased in the four-month
period ended September 30, 2014
compared with the three-month period ended August 31, 2013 due to an additional month in the
period as well as the addition of senior executives who were not
employed at Aptose in the three months ended August 31, 2013.
Stock-based compensation costs increased in the
four months ended September 30, 2014
compared with the three months ended August
31, 2013 due to option grants during the four-month period
compared with no option grants in the three-month period in the
prior year.
Aptose utilized cash of $3.9 million in operating activities in the four
months ended September 30, 2014
compared with $933 thousand in the
three months ended August 31,
2013. The increase in cash used in operating activities
during the four-month period is primarily related to an increased
net loss as well as a reduction in accounts payable and accrual
balances compared with the three months ended August 31, 2013.
At September 30,
2014 Aptose had cash and cash equivalents and short-term
investments of $33.1 million compared
to $30.4 million at May 31, 2014.
Subsequent to the four months ended September 30, 2014, the Board of Directors
approved a 1-for-12 share consolidation which became effective
October 1, 2014. The share
consolidation affected all of Aptose's common shares, stock options
and warrants outstanding at the effective time. Fractional
shares were not issued. Prior to consolidation there were
approximately 139 million shares outstanding and following the
share consolidation, there are approximately 11.6 million common
shares outstanding. Similarly, prior to consolidation, Aptose
had approximately 17.1 million stock options and 2.6 million
warrants to purchase common shares outstanding. Following the
share consolidation, there are approximately 1.4 million stock
options and 218 thousand warrants to purchase common shares
outstanding.
For further details and to view Aptose's
May 31, 2014 Audited Consolidated
Financial Statements and Management's Discussion and Analysis,
please see Aptose's filings on www.sedar.com and
on www.aptose.com.
|
|
|
|
Aptose Biosciences Inc. |
|
|
|
Condensed Consolidated Interim
Statements of Loss and Comprehensive Loss |
|
(unaudited) |
|
(amounts in 000's of Canadian Dollars except for per common
share data)
|
Four
months ended
Sep. 30, 2014 |
|
Three
months ended
Aug. 31, 2013 |
|
|
|
|
REVENUE |
$
- |
|
$
- |
|
|
|
|
EXPENSES |
|
|
|
Research and development |
1,311 |
|
615 |
General and administrative |
3,000 |
|
451 |
Operating expenses |
4,311 |
|
1,066 |
Finance expense |
37 |
|
36 |
Finance income |
(161) |
|
(1) |
Net financing expense (income) |
(124) |
|
35 |
Net loss and total comprehensive loss for the
period |
4,187 |
|
1,101 |
Basic and diluted loss per common
share |
$
0.36 |
|
$
0.31 |
|
|
|
|
Weighted average number of common
shares |
|
|
|
outstanding used
in the calculation of |
|
|
|
basic and
diluted loss per common share (000's) |
11,610 |
|
3,521 |
|
|
|
|
CONFERENCE CALL AND WEBCAST
Aptose will host a conference call to discuss
results for the four months ended September
30, 2014 on Tuesday, November 4,
2014 at 5:00 p.m. EDT.
Participants can access the conference call by dialing
1-888-231-8191 (North American toll free number) or 647-427-7450
(local). The conference call will be available via a live
webcast at
http://www.newswire.ca/en/webcast/detail/1435873/1595769, and will
also be available through a link on the Investor Relations section
of Aptose's website at http://www.aptose.com/events/. Please
log on to the webcast at least 10 minutes prior to the start of the
call to ensure time for any software downloads that may be
required. An archived version of the webcast will be available
on the Company's website for 30 days. An audio replay of the
webcast will be available approximately two hours after the
conclusion of the call for 30 days by dialing 1-855-859-2056, using
the passcode 28685150.
NOTE
The information contained in this news release
is unaudited.
About Aptose
Aptose Biosciences is a clinical-stage
biotechnology company committed to discovering and 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 research, coupled with
companion diagnostics to identify the optimal patient population
for our products. The Company's small molecule cancer therapeutics
pipeline includes products designed to provide enhanced efficacy
with existing anti-cancer therapies and regimens without
overlapping toxicities. Aptose Biosciences Inc. is listed on NASDAQ
under the symbol APTO and on the TSX under the symbol APS.
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 Aptose'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 expressed or implied factors
include, among others: changes in our stock price; our ability to
meet listing requirements; 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; stock market
volatility; 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.
SOURCE Aptose Biosciences Inc.
PDF available at:
http://stream1.newswire.ca/media/2014/11/04/20141104_C9365_DOC_EN_43173.pdf