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EntreMed's Aurora Kinase Inhibitor Induces Tumor Regression in,Preclinical Models

ture financial or business performance (including the timing of royalty revenues and future R&D expenditures), strategies, expectations and goals. Forward-looking statements are subject to numerous assumptions, risks and uncertainties, which change over time. Forward-looking statements speak only as of the date they are made, and no duty to update forward-looking statements is assumed. Actual results could differ materially from those currently anticipated due to a number of factors, including those set forth in Securities and Exchange Commission filings under "Risk Factors," including risks relating to the need for additional capital and the uncertainty of additional funding; variations in actual sales of Thalomid(R), risks associated with the Company's product candidates; the early-stage products under development; results in preclinical models are not necessarily indicative of clinical results, uncertainties relating to preclinical and clinical trials; success in the clinical development of any products; dependence on third parties; future capital needs; and risks relating to the commercialization, if any, of the Company's proposed products (such as marketing, safety, regulatory, patent, product liability, supply, competition and other risks).

     CONTACT:

     Ginny Dunn

     EntreMed, Inc.

     Associate Director

     Corporate Communications &

     Investor Relations

     (240) 864-2643

CONTACT: Ginny Dunn, Associate Director Corporate Communications &Investor Relations, of EntreMed, Inc., +1-240-864-2643

Web site: http://www.entremed.com/

Ticker Symbol: (NASDAQ-NMS:ENMD)

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