Cardiome Reports Second Quarter Results
11 Agosto 2009 - 8:45AM
PR Newswire (US)
NASDAQ: CRME TSX: COM VANCOUVER, Aug. 11 /PRNewswire-FirstCall/ --
Cardiome Pharma Corp. (NASDAQ: CRMENASDAQ:/NASDAQ:TSX:NASDAQ:COM)
today reported financial results for the second quarter ended June
30, 2009. Amounts, unless specified otherwise, are expressed in
Canadian dollars and in accordance with Canadian Generally Accepted
Accounting Principles (Canadian GAAP). At close of business on June
30, 2009, the exchange rate was CAD$1.00=US$0.8598. Results of
Operations We recorded a net loss of $1.4 million ($0.02 per common
share) for the three months ended June 30, 2009 ("Q2-2009"),
compared to a net loss of $18.1 million ($0.28 per common share)
for the three months ended June 30, 2008 ("Q2-2008"). The decrease
in net loss for the current quarter was largely due to decreased
research and development expenditures related to vernakalant (oral)
and GED-aPC clinical activities, initial amortization of deferred
revenue related to the upfront payment of U.S. $60 million from
Merck, which was recorded as licensing fees, and foreign exchange
gain on translation of the U.S. denominated upfront payment from
Merck. Revenue for Q2-2009 was $8.6 million, an increase of $8.4
million from $0.2 million in Q2-2008. We recorded $7.9 million for
Q2-2009 as amortization of the deferred revenue related to the
upfront payment from Merck. No milestone payments were received or
recognized in Q2-2008. Research and development expenditures were
$6.3 million for Q2-2009 compared to $12.9 million for Q2-2008. The
decrease of $6.6 million in Q2-2009 was primarily due to the
completion of the Phase 2b trial for vernakalant (oral) in fiscal
2008. General and administration expenditures for Q2-2009 were $5.0
million, compared to $4.4 million for Q2-2008. Amortization for
Q2-2009 was $0.8 million compared to $1.0 million for Q2-2008.
Interest and other income for Q2-2009 and Q2-2008 was $0.1 million.
Foreign exchange gain was $2.1 million in Q2-2009 compared to a
foreign exchange loss of $0.1 million in Q2-2008. Stock-based
compensation, a non-cash item included in operating expenses,
decreased to $0.4 million for Q2-2009, as compared to $1.0 million
for Q2-2008. Liquidity and Outstanding Share Capital At June 30,
2009, we had cash and cash equivalents of $82.0 million. As of
August 10, 2009, the Company had 63,859,246 common shares issued
and outstanding, 2,272,727 Series A preferred shares, and 4,700,112
common shares issuable upon the exercise of outstanding stock
options at a weighted-average exercise price of $8.39 per share.
Agreement with Merck Co., Inc. In April 2009, we announced a
collaboration and license agreement with Merck Co., Inc. for the
development and commercialization of vernakalant. The agreement
provides Merck with exclusive global rights to vernakalant (oral),
and provides a Merck affiliate with exclusive rights outside of the
United States, Canada and Mexico to vernakalant (iv). The agreement
became effective in May 2009, triggering an initial payment to us
of U.S. $60 million. Subsequent to quarter-end, in July 2009 we
announced that we earned a further U.S. $15 million milestone
payment triggered by the submission, by a Merck affiliate, of a
Marketing Authorisation Application (MAA) to the European Medicines
Agency (EMEA) seeking marketing approval for vernakalant (iv) in
the European Union. Further terms of the Merck agreement are
outlined in our press release dated April 8, 2009. Conference Call
Notification Cardiome will hold its quarterly teleconference and
webcast at 9:00am Eastern (6:00am Pacific) on Tuesday, August 11,
2009. To access the conference call, please dial 416-340-2217 or
866-696-5910 and reference conference 2345242. There will be a
separate dial-in line for analysts on which we will respond to
questions at the end of the call. The webcast can be accessed
through Cardiome's website at http://www.cardiome.com/. Webcast and
telephone replays of the conference call will be available
approximately two hours after the completion of the call through
September 11, 2009. Please dial 416-695-5800 or 800-408-3053 and
enter code 3147267 followed by the number sign to access the
replay. About Cardiome Pharma Corp. Cardiome Pharma Corp. is a
product-focused drug development company dedicated to the
advancement and commercialization of novel treatments for disorders
of the heart and circulatory system. Cardiome is traded on the
NASDAQ National Market (CRME) and the Toronto Stock Exchange (COM).
For more information, please visit our web site at
http://www.cardiome.com/. Forward-Looking Statement Disclaimer
Certain statements in this press release contain forward-looking
statements within the meaning of the Private Securities Litigation
Reform Act of 1995 or forward-looking information under applicable
Canadian securities legislation that may not be based on historical
fact, including without limitation statements containing the words
"believe", "may", "plan", "will", "estimate", "continue",
"anticipate", "intend", "expect" and similar expressions. Such
forward-looking statements or information involve known and unknown
risks, uncertainties and other factors that may cause our actual
results, events or developments, or industry results, to be
materially different from any future results, events or
developments expressed or implied by such forward-looking
statements or information. Such factors include, among others, our
stage of development, lack of product revenues, additional capital
requirements, risk associated with the completion of clinical
trials and obtaining regulatory approval to market our products,
the ability to protect our intellectual property, dependence on
collaborative partners and the prospects for negotiating additional
corporate collaborations or licensing arrangements and their
timing. Specifically, certain risks and uncertainties that could
cause such actual events or results expressed or implied by such
forward-looking statements and information to differ materially
from any future events or results expressed or implied by such
statements and information include, but are not limited to, the
risks and uncertainties that: we, together with our collaborative
partners, may not be able to successfully develop and obtain
regulatory approval for vernakalant (iv) or vernakalant (oral) in
the treatment of atrial fibrillation or any other current or future
products in our targeted indications; our future operating results
are uncertain and likely to fluctuate; we may not be able to raise
additional capital; we may not be successful in establishing
additional corporate collaborations or licensing arrangements; we
may not be able to establish marketing and sales capabilities and
the costs of launching our products may be greater than
anticipated; we rely on third parties for the continued supply and
manufacture of vernakalant (iv) and vernakalant (oral) and we have
no experience in commercial manufacturing; we may face unknown
risks related to intellectual property matters; we face increased
competition from pharmaceutical and biotechnology companies; and
other factors as described in detail in our filings with the
Securities and Exchange Commission available at http://www.sec.gov/
and the Canadian securities regulatory authorities at
http://www.sedar.com/. Given these risks and uncertainties, you are
cautioned not to place undue reliance on such forward-looking
statements and information, which are qualified in their entirety
by this cautionary statement. All forward-looking statements and
information made herein are based on our current expectations and
we undertake no obligation to revise or update such forward-looking
statements and information to reflect subsequent events or
circumstances, except as required by law. DATASOURCE: Cardiome
Pharma Corp. CONTACT: Peter K. Hofman, Senior Director, Investor
Relations, (604) 676-6993 or Toll Free: 1-800-330-9928, Email:
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