NASDAQ: CRME TSX: COM VANCOUVER, Aug. 12 /PRNewswire-FirstCall/ -- Cardiome Pharma Corp. (NASDAQ: CRME/TSX:NASDAQ:COM) today reported financial results for the second quarter ended June 30, 2008. 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, 2008, the exchange rate was CAD$1.00=US$0.9807. Results of Operations We recorded a net loss of $18.1 million ($0.28 per common share) for the three months ended June 30, 2008 ("Q2-2008"), compared to a net loss of $14.6 million ($0.23 per common share) for the three months ended June 30, 2007 ("Q2-2007"). The increase in net loss for the current quarter was largely due to lower licensing and research collaborative fees, and increased research and development expenditures related to vernakalant (oral), the European comparator study for vernakalant (iv) and GED-aPC clinical activities. Revenue for Q2-2008 was $0.2 million, a decrease of $0.9 million from $1.1 million in Q2-2007. Research and development expenditures were $12.8 million for Q2-2008, compared to $9.8 million for Q2 2007. General and administration expenses decreased to $4.4 million in Q2-2008 from $4.8 million in Q2-2007. Amortization was $1.1 million for Q2-2008 compared to $0.8 million for Q2-2007. Interest and other income was $0.1 million for Q2-2008 compared to $1.3 million for Q2-2007. Foreign exchange loss was $0.1 million for Q2-2008 compared to a loss of $1.6 million in Q2-2007. Stock-based compensation, a non-cash item included in operating expenses, decreased to $1.0 million for Q2-2008, as compared to $2.1 million for Q2-2007. Liquidity and Outstanding Share Capital At June 30, 2008, the Company had cash and cash equivalents of $31.0 million. Subsequent to quarter-end, in July 2008 we announced that CR Intrinsic Investments, LLC, an investment fund managed by CR Intrinsic Investors, LLC, an affiliate of S.A.C. Capital Advisors, LLC purchased Series A convertible preferred shares for gross proceeds of US$25 million. The transaction closed on July 25, 2008. As of August 12, 2008, the Company had 63,762,296 common shares issued and outstanding, 2,272,727 Series A preferred shares, and 4,949,562 common shares issuable upon the exercise of outstanding stock options at a weighted-average exercise price of $8.38 per share. Conference Call Notification Cardiome will hold a teleconference and webcast on Tuesday, August 12, 2008 at 4:30pm Eastern (1:30pm Pacific). To access the conference call, please dial 416-641-6117 or 866-299-6655. 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 12, 2008. Please dial 416-695-5800 or 800-408-3053 and enter code 3268411 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 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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