Response Biomedical Corporation Announces Third Quarter Results 2009-11-10 07:00 ET - News Release -
Total revenues double over last year’s comparable nine months
-
Clinical products revenue up 139% over last year’s comparable nine
months
 Company Website:
http://www.responsebio.com VANCOUVER -- (Business Wire)
Response
Biomedical Corporation (TSX: RBM, OTCBB: RPBIF) today announced
financial results for the third quarter and nine months ended September
30, 2009.
Total revenues for the three and nine month periods ended September 30,
2009 increased 39% and 106% to $2,047,523 and $7,495,339, respectively,
compared to $1,471,130 and $3,641,766 for the same periods in 2008.
Given the success of our commercial partners’ efforts, clinical products
revenue showed the largest growth at 62% and 139% to $1,688,423 and
$5,236,438 for the three and nine month periods ended September 30,
2009, respectively, compared to $1,040,649 and $2,191,409 for the same
periods in 2008.
Net loss for the three and nine month periods ended September 30, 2009
was reduced by 14% and 38% to $3,177,221 and $6,807,623, respectively,
compared to $3,684,602 and $10,969,207 for the same periods in 2008.
Expenses were reduced by 15% and 29% to $2,813,195 and $7,552,556,
respectively, for the three and nine month periods ended September 30,
2009, compared to $3,294,694 and $10,636,832 for the same periods in
2008.
“We are on track to conclude our best year ever, with total revenues at
September 30, 2009 well in excess of total revenues for all of 2008. As
we work with our partners and global distributors to introduce the RAMP®
technology to a growing international market, we see this trend
continuing in 2010 and beyond,” said S. Wayne Kay, Chief Executive
Officer. “Looking at our strengthened cash position, we had
approximately $7.5 million in cash and cash equivalents as at September
30, 2009, compared to $2.3 million as at December 31, 2008,” said S.
Wayne Kay, Chief Executive Officer. “Our working capital as at September
30, 2009 was approximately $9.0 million compared to $2.9 million as at
December 31, 2008. As you can see, we continue to show strong revenue
growth, quarter over quarter when compared to revenues from last year.”
Conference Call Information
Response Biomedical management will host an analyst conference
call beginning at 10:00 a.m. (Eastern Time) today to discuss these
results and other corporate matters. During the conference call, the
Company may discuss and answer questions concerning business and
financial developments and trends.
The analyst conference call may be accessed by dialing 1-416-981-9000
(domestic and international) or 1-800-954-0691 (toll free in North
America). An access code is not required. It is also available to listen
via Web cast at http://www.snwebcastcenter.com/event/?event_id=589.
An archive of the call will be available from the same link
approximately two hours after the live call has concluded and will be
accessible for 30 days.
About Response Biomedical
Response Biomedical develops, manufactures and markets rapid on-site
diagnostic tests for use with its RAMP® Platform for clinical
and environmental applications. RAMP® represents a new
paradigm in diagnostics that provides high sensitivity and reliable
information in minutes. It is ideally suited to both point of care
testing and laboratory use.
The RAMP® system consists of a Reader and single-use
disposable test cartridges, and has the potential to be adapted to more
than 250 medical and non-medical tests currently performed in
laboratories. RAMP® clinical tests are commercially available
for the early detection of heart attack, congestive heart failure,
influenza and RSV through our commercial partners, Roche and 3M Health
Care respectively.
In the non-clinical market, RAMP® Tests are currently
provided for the environmental detection of West Nile Virus, and
Biodefense applications including the rapid on-site detection of
anthrax, smallpox, ricin and botulinum toxin. Several other product
applications are under development.
Response has achieved CE Marking for its Reader and clinical tests and
its Quality Management System is registered to ISO 13485: 2003 and ISO
9001: 2000.
Response Biomedical is a publicly traded company, listed on the TSX
under the trading symbol "RBM" and quoted on the OTC Bulletin Board
under the symbol "RPBIF". For further information, please visit the
Company's website at www.responsebio.com.
Statements contained in this press release relating to future
results, events or developments, for example, statements containing the
words "believes," "may," "could", "plans," "will," "estimate,"
"continue," "anticipates," "intends," "expects", “goal” and similar
expressions, are "forward-looking statements" or “forward-looking
information” under applicable United States and Canadian securities laws.Forward-looking statements or information may involve, but are not
limited to, comments with respect to our planned activities, business
plan and strategies and their future implementation, and our
expectations for our financial condition and the results of, or outlook
for, our business operations generally. Forward-looking statements or
information are subject to the related assumptions made by us and
involve known and unknown risks, uncertainties and other factors that
may cause actual results, events or developments to be materially
different from those expressed or implied by such statements or
information. Many of such risks, uncertainties and other factors form part of our
underlying assumptions, and include, among other things, financial risks
that would affect our operations such as our limited available working
capital and cash flows and whether and for how long available funds will
be sufficient to fund our operations and our ability to raise additional
capital as and when needed; our need for substantial additional funding
to conduct research and development and commercialization activities;
current financial market conditions which may negatively affect our
ability to obtain financing; changing facility costs and other risks
relating to our facilities expansion plans; our ability to establish,
and our dependence upon, relationships with strategic alliance partners
to develop and commercialize products; technological changes that impact
our existing products or our ability to develop and commercialize our
products; our ability to obtain and enforce timely patent and other
intellectual property protection for our technology and products;our
ability to obtain and maintain rights to technology from licensors;
liability for patent, product liability and other claims asserted
against us; commercialization limitations imposed by patents owned or
controlled by third parties; technical risk in research and development;
adverse results or unexpected delays in product development and clinical
trials; our ability to retain, and our reliance upon, third party
suppliers, manufacturers, distributors and alliance partners; our
ability to attract and retain qualified personnel; our ability to
effectively and efficiently manage the planned growth of our operations;
our ability to obtain, and the timing of, necessary regulatory
approvals; our ability to profitably sell our products at prices that
would be acceptable to third-party reimbursement programs; competition
including competition from others with significantly more resources;
market acceptance of our products and the size of our markets; changes
in business strategy or development plans; changes in, or the failure to
comply with, governmental regulations; fluctuations in interest rates
and foreign exchange rates; seasonality including government budget
cycles; general economic and business conditions where we operate; and
other factors referenced in our annual report, our Annual Information
Form (AIF) (Form 20-F in the U.S.) and other filings with Canadian and
United States securities regulatory authorities. Given these uncertainties, assumptions and risks, readers are
cautioned not to place undue reliance on such forward-looking statements
or information. We disclaim any obligation to update, or to publicly
announce any revisions to, any such statements or information to reflect
future results, events or developments, except as required by law. |
|
|
| |
| | | | | | Three Months Ended September 30, | | Nine Months Ended September 30, | |
|
|
|
| 2009 |
| 2008 |
| 2009 |
| 2008 | |
CLINICAL PRODUCTS REVENUE
|
|
|
| $ | 1,688,423 |
|
$
|
1,040,649
|
| $ | 5,236,438 |
|
$
|
2,191,409
| |
NON CLINICAL PRODUCTS REVENUE
|
|
|
| $ | 260,954 |
|
$
|
331,309
|
| $ | 1,059,710 |
|
$
|
1,124,641
| |
CONTRACT SERVICE FEES
|
|
|
| $ | 98,146 |
|
$
|
99,172
|
| $ | 1,199,191 |
|
$
|
325,716
| | TOTAL REVENUES |
|
|
| $ | 2,047,523 |
| $ | 1,471,130 |
| $ | 7,495,339 |
| $ | 3,641,766 | |
EXPENSES
|
|
|
| $ | 2,813,195 |
|
$
|
3,294,694
|
| $ | 7,552,556 |
|
$
|
10,636,832
| |
LOSS FOR THE PERIOD
|
|
|
| $ | 3,177,221 |
|
$
|
3,684,602
|
| $ | 6,807,623 |
|
$
|
10,969,207
| |
LOSS PER SHARE
|
|
|
| $ | 0.01 |
|
$
|
0.03
|
| $ | 0.03 |
|
$
|
0.08
|
Contacts:
Response Biomedical Corporation Bill Wickson, 604-456-6073 Director,
Investor Relations bwickson@responsebio.com Source: Response Biomedical Corporation |