EPIX Pharmaceuticals Receives Audit Opinion Containing Going Concern Qualification

EPIX Pharmaceuticals Receives Audit Opinion Containing Going Concern Qualification

LEXINGTON, Mass. -- Mar. 25, 2009-- EPIX Pharmaceuticals, Inc. a biopharmaceutical company focused on discovering and developing novel therapeutics through the use of its proprietary and highly efficient in silico drug discovery platform today announced that its Form 10-K filed with the Securities and Exchange Commission on March 13, 2009 included a going concern qualification from its independent registered accounting firm, Ernst & Young LLP.

This announcement is being made in order to comply with Nasdaq Marketplace Rule 4350(b)(1)(B), which requires a Nasdaq-listed issuer that receives an audit opinion that contains a going concern qualification to make a public announcement to that effect. This announcement does not represent any change or amendment to the company's 2008 financial statements or to its Annual Report on Form 10-K.

About EPIX

EPIX Pharmaceuticals is a biopharmaceutical company focused on discovering and developing novel therapeutics through the use of its proprietary and highly efficient in silico drug discovery platform. The company has a pipeline of internally-discovered drug candidates currently in clinical development to treat diseases of the central nervous system (see www.trialforAD.com) and lung conditions. EPIX also has collaborations with leading organizations, including GlaxoSmithKline, Amgen and Cystic Fibrosis Foundation Therapeutics. For more information, please visit the company's website at www.epixpharma.com.

 

Source: EPIX Pharmaceuticals, Inc.

EPIX
Kim C. Drapkin, 781-761-7602
Chief Financial Officer
or
Pure Communications
Jennifer Beugelmans, 646-596-7473
 
 
This website contains certain express or implied forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 that are subject to known and unknown risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statement. Those risks and uncertainties include, among other things: the risk that we may fail to comply with regulations relating to our products and product candidates, including FDA requirements; our inability to successfully in-license products and/or technologies; our inability to identify and interest potential partners in our technologies and products, particularly EP-2104R; our inability to successfully defend against litigation, including any appeal or re-filing of the shareholder class action lawsuit; our inability to protect our intellectual property and the cost of enforcing or defending our intellectual property rights; the risk that we will not successfully integrate Predix's business; our inability to further identify, develop and achieve commercial success for new products and technologies; the possibility of delays in the research and development necessary to select drug development candidates and delays in clinical trials; the risk that clinical trials may not result in marketable products; the risk that we may be unable to successfully secure regulatory approval of and market our drug candidates; the risks associated with reliance on outside financing to meet capital requirements; risks associated with new and uncertain technology; the development of competing systems; and risks of new, changing and competitive technologies and regulations in the U.S. and internationally. You are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof.

We undertake no obligation to update or revise the information contained on this website, whether as a result of new information, future events or circumstances or otherwise. For additional information regarding these and other risks that we face, see the disclosure contained in our filings with the Securities and Exchange Commission.