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Questcor To Commence Phase 2 Study of Acthar for Acute Respiratory Distress Syndrome
Date:10/22/2013

events or results may differ materially. Factors that could cause or contribute to such differences include, but are not limited to, the following:

  • Research and development risks, including risks associated with our work in the area of ARDS, our reliance on third-parties to conduct research and development, and the ability of research and development to generate successful results;
  • Our reliance on Acthar for substantially all of our net sales and profits and the possible FDA approval and market introduction of competitive products;
  • The lack of patent protection for Acthar;
  • Our ability to effectively manage our growth, including the expansion of our sales forces, planned international expansion, recent acquisitions, and our reliance on key personnel;
  • The risk of product liability lawsuits;
  • Other risks discussed in Questcor's annual report on Form 10-K for the year ended December 31, 2012 as filed with the Securities and Exchange Commission, or SEC, on February 27, 2013, and other documents filed with the SEC.

The risk factors and other information contained in these documents should be considered in evaluating Questcor's prospects and future financial performance.

Questcor undertakes no obligation to publicly release the result of any revisions to these forward-looking statements, which may be made to reflect events or circumstances after the date of this release.


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SOURCE Questcor Pharmaceuticals, Inc.
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