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Hollis-Eden Announces Cancellation of Acute Radiation Syndrome RFP,by Department of Health and Human Services

ditional next-generation candidate, HE3235, has also been selected for clinical development in cancer. For more information on Hollis-Eden, visit the Company's website at www.holliseden.com.

This press release contains forward-looking statements within the meaning of the federal securities laws concerning, among other things, the potential and prospects of the Company's drug discovery program and its drug candidates. Any statement included in this press release that are not a description of historical facts are forward-looking statements that involve risks, uncertainties, assumptions and other factors which, if they do not materialize or prove correct, could cause the Company's actual results to differ materially from historical results or those expressed or implied by such forward-looking statements. Such statements are subject to certain risks and uncertainties inherent in the Company's business, including, but not limited to: the ability to complete preclinical and clinical trials successfully and within specified timelines, if at all; the ability to obtain regulatory approval for NEUMUNE under the U.S. Food and Drug Administration Animal Efficacy Rule, even if shown to be effective in preclinical studies; the ability to receive any stockpiling orders for NEUMUNE from the U.S. federal, state and foreign governments or agencies, even if approved by regulatory authorities; the Company's future capital needs; the Company's ability to obtain additional funding; the ability of the Company to protect its intellectual property rights and to not infringe the intellectual property rights of others; the development of competitive products by other companies; and other risks detailed from time to time in the Company's filings with the Securities and Exchange Commission. Existing and prospective investors are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date of this press release. Except as required by law, the
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(Date:10/6/2008)...he door to the understanding of and possible ...ancer, BILLERICA, Mass., Oct. 6 /- S...the first ever analytical instrument for the,kinet... and cytoplasmic,glycolysis in cells in a 96 well ...ing cellular bioenergetics have been relatively un...
(Date:10/6/2008)...tudies with Durezol Dosed Prior to Surgery, TAMPA..., Inc., a,privately held ophthalmic-focused biopha...TM) (difluprednate ophthalmic emulsion) 0.05% is n...oved by the U.S. Food and,Drug Administration in J...ndicated for the treatment of inflammation and pai...
(Date:10/6/2008)...ll Scheduled for 9:00 AM ET Today -, SEATTLE, Oct... (Nasdaq:,DNDN) announced today that it has comple...andomized, double-blind, placebo-controlled IMPACT...ent, also known as D9902B),clinical trial designed...ational active cellular immunotherapy PROVENGE(R) ...
(Date:10/6/2008)...at drinking polyphenol-rich 100% Concord grape,jui...ergy intake or body,weight, CONCORD, Mass., Oct. ...phenol-rich Concord grape juice did not cause sign...es in appetite and was shown to reduce waist,circu...th Annual Meeting of,the American College of Nutri...
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...ly to subsequently,respond, have substantially mor...ange in treatment strategy, COLORADO SPRINGS, Colo...ta presented at the 2007 International Congress on...sychotic drug,response be assessed earlier than is...zophrenia treatment paradigm for when to,evaluate ...
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