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Cardiome Updates Guidance
Date:11/26/2007

NASDAQ: CRME TSX: COM

VANCOUVER, Nov. 26 /PRNewswire-FirstCall/ - Cardiome Pharma Corp. (NASDAQ: CRME / TSX: COM) today announced updated guidance for expected interim results from its Phase 2b clinical trial for vernakalant (oral). Cardiome had originally intended to complete and disclose the interim analysis in the fourth quarter of 2007. The Company has decided to complete and disclose the interim analysis in March 2008, with the final study results to be presented in mid-2008.

"While we remain blinded to the efficacy data from the ongoing study, we do know that a significant proportion of our enrollment has occurred in the past two months, meaning that those patients have not yet progressed deeply into the 90-day program," stated Doug Janzen, President and Chief Business Officer of Cardiome. "By delaying one quarter we expect to add roughly 20 percent more patients into the interim analysis than originally planned, and as a result more data will be available on patients with longer-term exposure. More than 400 patients have been randomized in the study, and enrollment is expected to be complete in early 2008."

"In the context of current business development activities and corporate discussions, we have decided that generating a very robust interim analysis with a large number of patients is in the best interests of shareholders," stated Bob Rieder, Chairman and Chief Executive Officer of Cardiome. "While we are all looking forward to seeing data from this study as soon as possible, we believe that the larger dataset that we can gather under this revised timeline will be highly beneficial in our efforts to drive shareholder value in the first half of 2008. In accordance with our disclosure practice, we will release the results of the interim analysis in a timely manner upon receipt of un-blinded results."

The Phase 2b clinical trial of vernakalant (oral) for the prevention of recurrence of atrial fibrillat
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SOURCE Cardiome Pharma Corp.
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