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Adeona Executes Agreement to Initiate Phase IIb Clinical Trial of Proprietary Zinc-Based Therapy in Lou Gehrig's Disease (ALS)
Date:6/23/2011

nts are based upon current beliefs, expectations and assumptions and are subject to a number of risks and uncertainties, many of which are difficult to predict and include statements regarding the planned Phase llb clinical trial, the ability to conduct the clinical trial under an IND application, the suggested role of zinc in the treatment of  ALS, the planned primary and secondary endpoints and the anticipated number of clinical trial centers and enrolled patients. The forward-looking statements are subject to risks and uncertainties that could cause actual results to differ materially from those set forth or implied by any forward-looking statements. Important factors that could cause actual results to differ materially from those reflected in Adeona's forward-looking statements include, among others, our failure to obtain regulatory approval or market approval of the use of AEN-100 and AEN-200 in the treatment of ALS, failure to obtain approval to conduct the trial under the IND , failure of the clinical trial evaluating AEN-100 and AEN-200 to have favorable result such as  a failure to show benefits of zinc therapy in ALS patients, a failure of the treatment group to have a decrease in toxicity from unbound glutamate or a  failure of ALS patients treated with our proprietary zinc to successfully meet the planned primary and secondary endpoints,  and other factors described in Adeona's report on Form 10-K for the year ended December 31, 2010 and any other filings with the SEC. The information in this release is provided only as of the date of this release, and Adeona undertakes no obligation to update any forward-looking statements contained in this release on account of new information, future events, or otherwise, except as required by law.


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SOURCE Adeona Pharmaceuticals, Inc.
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