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Jazz Pharmaceuticals and UCB Announce Second Phase III Study of Sodium Oxybate in Patients With Fibromyalgia Meets Primary Endpoints
Date:6/24/2009

d uncertainties, which include, without limitation, risks related to the outcome of further analysis of the data from the study, risks related to the company's financial position and default on its senior debt, and risks that regulatory filings may not be made, or may be delayed, and that the sodium oxybate (JZP-6) product candidate may not be approved for marketing for the treatment of fibromyalgia by regulatory authorities. These and other risk factors are discussed under "Risk Factors" in the Quarterly Report on Form 10-Q for the quarter ended March 31, 2009 filed by Jazz Pharmaceuticals with the Securities and Exchange Commission on May 7, 2009. Jazz Pharmaceuticals undertakes no duty or obligation to update any forward-looking statements contained in this release as a result of new information, future events or changes in its expectations.

UCB Forward-looking Statement

This press release contains forward-looking statements based on current plans, estimates and beliefs of management. Such statements are subject to risks and uncertainties that may cause actual results to be materially different from those that may be implied by such forward-looking statements contained in this press release. Important factors that could result in such differences include: changes in general economic, business and competitive conditions, effects of future judicial decisions, changes in regulation, exchange rate fluctuations and hiring and retention of employees.


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SOURCE Jazz Pharmaceuticals, Inc.; UCB
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