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Genta Completes Appeal of FDA Decision for Genasense(R) in CLL
Date:10/25/2007

- the Company's ability to obtain necessary regulatory approval for

Genasense(R) from the U.S. Food and Drug Administration ("FDA") or

European Medicines Agency ("EMEA");

- the safety and efficacy of the Company's products or product candidates;

- the Company's assessment of its clinical trials;

- the commencement and completion of clinical trials;

- the Company's ability to develop, manufacture, license and sell its

products or product candidates;

- the Company's ability to enter into and successfully execute license and

collaborative agreements, if any;

- the adequacy of the Company's capital resources and cash flow

projections, and the Company's ability to obtain sufficient financing to

maintain the Company's planned operations;

- the adequacy of the Company's patents and proprietary rights;

- the impact of litigation that has been brought against the Company and

its officers and directors and any proposed settlement of such

litigation; and

- the other risks described under Certain Risks and Uncertainties Related

to the Company's Business, as contained in the Company's Annual Report

on Form 10-K and Quarterly Report on Form 10-Q.

The Company does not undertake to update any forward-looking statements. There are a number of factors that could cause actual results and developments to differ materially. For a discussion of those risks and uncertainties, please see the Company's Annual Report on Form 10-K for 2006 and its most recent quarterly report on Form 10-Q.

CONTACT:

Brian Korb

The Trout Group

908-286-3980

info@genta.com


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SOURCE Genta Incorporated
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