QUEBEC CITY, Sept. 11, 2014 /PRNewswire/ - DiagnoCure, Inc.
(TSX: CUR) (OTCQX: DGCRF) (the "Corporation") today reported
financial and operational results for the third quarter 2014 ended
July 31, 2014. The Corporation
announced a net loss of $504,105 or
$0.01 per share for this quarter
compared with a loss of $595,262 or
$0.01 per share for the same period
last year. During the third quarter ended July 31, 2014, total revenues decreased by 19%
compared with the same quarter of 2013, due to a decrease in PCA3
royalties paid to DiagnoCure. Operating expenses decreased by
$127,318 or 16%, to $657,529 for the third quarter of 2014 from
$784,847 for the same period of 2013.
At the end of the quarter, cash and short-term investments stood at
$2,541,852.
Based in part upon recent recommendations by the American
Society for Clinical Pathology and the College of American
Pathologists, the United States Centers for Medicare and Medicaid
Services is expected to make a decision before the end of 2014
about the amount of reimbursement for PCA3 for calendar year 2015.
"This important milestone about reimbursement, the PCA3 test
inclusion in American and European guidelines, and several
business-related actions taken in the last months lead us to
believe that shareholders should expect a positive impact on PCA3
future sales and royalties," said Dr. Yves
Fradet, President and Chief Medical Officer of the
Corporation.
The results of the VITAR II retrospective clinical study of the
Previstage™ GCC test were published in the August 15, 2014
issue of the Clinical Cancer Research journal. This multicenter
study led by Dr. Dan Sargent of the
Mayo Clinic confirmed that the GCC status in lymph nodes of 366
stage II colon cancer patients can classify up to 60% of them as
having a very low (8%) risk of recurrence at five years suggesting,
that these patients may gain little benefit from toxic adjuvant
chemotherapy. The Previstage™ GCC colorectal cancer staging test is
now offered in Canada by
DiagnoCure's licensed medical biology laboratory.
The Corporation also has completed the enrollment of more than
500 patients in the clinical study of its new multi-marker prostate
cancer test that does not include PCA3. Collection of final
clinical data is underway and completion of data analysis is
expected before year's end.
Results of the Third Quarter 2014
Total revenues for the third quarter of 2014 were $153,424 compared with $189,585 for the same period of 2013. This
decrease of $36,161 or 19% is mostly
attributable to PCA3 royalties, reflecting a decrease in U.S.
royalty revenues.
Operating expenses decreased by $127,318, to $657,529 for the third quarter of 2014 from
$784,847 for the same period of 2013.
This decrease is mainly attributable to reduction in professional
fees and amortization of the intangible asset. Total operating
expenses decreased primarily as a result of the following:
- Research and development expenses, net of investment tax
credits, decreased by $55,243, to
$307,294 for the third quarter of
2014 from $362,537 for the same
period of 2013. This decrease in research and development expenses
is attributable to the amortization charge of the GCC intangible
asset following the review of its useful life and to the
amortization of the Shc intangible asset, since the Corporation
recognized a full impairment charge in the last quarter of fiscal
year 2013. Without the amortization charges of intangible assets,
the research and development expenses increased by $74,874 to $237,637
for the third quarter of 2014 compared to $162,763 for the same period of 2013. This
increase is mainly attributable to the new multi-marker prostate
cancer test.
- General and administrative expenses decreased by $69,678, to $305,660 for the third quarter of 2014 from
$375,338 for the same period of 2013.
This decrease is attributable to reduction in professional
fees.
Financial Data
|
For the three
months periods ended
July
31
|
2014
|
2013
|
|
$
|
$
|
License and royalty
revenues
|
153,424
|
189,585
|
Total
revenues
|
153,424
|
189,585
|
Operating expenses
(before stock-based compensation, depreciation and
amortization)
|
560,277
|
541,338
|
Net loss (before
stock-based compensation, depreciation and amortization)
|
(406,853)
|
(351,753)
|
Stock-based
compensation
|
13,513
|
26,929
|
Depreciation of
property, plant and equipment
|
14,082
|
16,806
|
Amortization of
intangible asset
|
69,657
|
199,774
|
Net loss and
comprehensive loss
|
(504,105)
|
(595,262)
|
Basic and diluted net
loss per share
|
(0.01)
|
(0.01)
|
Weighted average
number of common shares outstanding
|
43,040,471
|
43,040,471
|
Consolidated Balance Sheets
|
July 31,
2014
|
October 31,
2013
|
|
$
|
$
|
Cash and short term
investments
|
2,541,852
|
4,190,296
|
Total
assets
|
5,958,079
|
7,849,267
|
Shareholders'
equity
|
5,490,473
|
7,009,261
|
Number of commons
shares outstanding
|
43,040,471
|
43,040,471
|
About DiagnoCure
DiagnoCure (TSX: CUR; OTCQX: DGCRF) is a life science
corporation that develops and provides molecular and genomic tests
to support effective clinical decisions enabling personalized
medicine in oncology. In 2008, the Corporation launched a
colorectal cancer staging test through its U.S. CLIA laboratory.
PrevistageTM GCC is currently available for licensing.
The Corporation has granted a worldwide exclusive license on the
diagnostic applications of its proprietary molecular biomarker PCA3
to Gen-Probe, now a wholly-owned subsidiary of Hologic Inc. Hologic
Gen-Probe's PROGENSA® PCA3 prostate cancer test is commercialized
in Europe under CE mark and is
approved for commercialization in Canada and the
United States. For more information, please visit
www.diagnocure.com.
Forward‐looking statements
This release may contain forward‐looking statements that involve
known and unknown risks, uncertainties and assumptions that may
cause actual results to differ materially from those expected.
Forward-looking statements can be identified by the use of the
conditional or forward-looking terminology such as "anticipates",
"assumes", "believes", "estimates", "expects", "intend", "may",
"plans", "projects", "should", "will", or the negative thereof or
other variations thereon. Forward-looking statements also include
any other statements that do not refer to historical facts. All
such forward-looking statements are made pursuant to the
"safe-harbour" provisions of applicable Canadian securities laws.
By their very nature, forward‐looking statements are based on
expectations and hypotheses and also involve risks and
uncertainties, known and unknown, many of which are beyond
DiagnoCure's control. Forward-looking statements are presented for
the purpose of assisting investors and others in understanding
certain key elements of the Corporation's current objectives,
strategic priorities, expectations and plans, and in obtaining a
better understanding of the Corporation's business and anticipated
operating environment. Readers are cautioned that such information
may not be appropriate for other purposes and that they should not
place undue reliance on these forward‐looking statements. For
instance, any forward-looking statements regarding the outcome of
research and development projects, clinical studies and future
revenues, including those related to PROGENSA® PCA3, are based on
management expectations and such outcome may vary materially
depending on global political and economic conditions, dependence
on collaboration partners, uncertainty of healthcare reimbursement,
and marketing and distribution challenges. In addition, the reader
is referred to the applicable general risks and uncertainties
described in DiagnoCure's most recent Annual Information Form under
the heading "Risk Factors". DiagnoCure undertakes no obligation to
publicly update or revise any forward‐looking statements contained
herein unless required by the applicable securities laws and
regulations.
SOURCE DiagnoCure inc.