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Human Genome Sciences Announces Positive Final Results Of Phase 2b,Trial of Albuferon

Section 21E of the Securities Exchange Act of 1934, as amended. The forward-looking statements are based on Human Genome Sciences' current intent, belief and expectations. These statements are not guarantees of future performance and are subject to certain risks and uncertainties that are difficult to predict. Actual results may differ materially from these forward-looking statements because of the Company's unproven business model, its dependence on new technologies, the uncertainty and timing of clinical trials, the Company's ability to develop and commercialize products, its dependence on collaborators for services and revenue, its substantial indebtedness and lease obligations, its changing requirements and costs associated with facilities and clinical trials, intense competition, the uncertainty of patent and intellectual property protection, the Company's dependence on key management and key suppliers, the uncertainty of regulation of products, the impact of future alliances or transactions and other risks described in the Company's filings with the Securities and Exchange Commission. In addition, the Company will continue to face risks related to animal and human testing, to the manufacture of ABthrax and to FDA concurrence that ABthrax meets the requirements of the ABthrax contract. If the Company is unable to meet the product requirements associated with the ABthrax contract, the U.S. Government will not be required to reimburse the Company for the costs incurred or to purchase any ABthrax doses. Existing and prospective investors are cautioned not to place undue reliance on these forward-looking statements, which speak only as of today's date. Human Genome Sciences undertakes no obligation to update or revise the information contained in this announcement whether as a result of new information, future events or circumstances or otherwise.

CONTACT: Jerry Parrott, Vice President, Corporate Communications,+1-301-315-2777, Kate de Santis, Director, Inv
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...rship Strengthened with Clinical Trials S...PANY, N.J. and ATLANTA, Sept. 6 Image Solutions,I...quire Zurich,Biostatistics, Inc. (ZBI). With the L...gulatory submissions, the acquisition further stre...Consortium (CDISC) capabilities,the FDA-supported ...
...tor to Enter Registration Trials, HAYWARD, Calif.... KOSN ) today announced that it has successfully,... Drug Administration,(FDA) on the design of its TI...s Hsp90 inhibitor tanespimycin as a treatment for ...Special Protocol Assessment (SPA),process, Kosan a...
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(Date:11/27/2009)...s to bring unprecedented medical, economic burdens...althDay News) -- The number of people with diabete...the next 25 years, a new study predicts. , That...on people with the disease, up from 23.7 million t... people with diabetes will triple, the study also ...
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...Weiss, breast oncologist and BREASTCANCER.ORG foun...t Cancer Patient Protection ACT, ...atory drive-through,mastectomies is an unconsciona...r and President of Breastcancer.org, in,an open le...
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