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Allos Therapeutics' PDX Granted Orphan Medicinal Product,Designation by the European Commission

X will not support an application for marketing approval in the European Union; and the risk that the Company may lack the financial resources and access to capital to fund future clinical trials for PDX or any of its other product candidates. Additional information concerning these and other factors that may cause actual results to differ materially from those anticipated in the forward-looking statements is contained in the "Risk Factors" section of the Company's Annual Report on Form 10-K for the year ended December 31, 2005 and in the Company's other periodic reports and filings with the Securities and Exchange Commission. The Company cautions investors not to place undue reliance on the forward-looking statements contained in this press release. All forward-looking statements are based on information currently available to the Company on the date hereof, and the Company undertakes no obligation to revise or update these forward-looking statements to reflect events or circumstances after the date of this presentation, except as required by law.

Note: EFAPROXYNTM and the Allos logo are trademarks of Allos Therapeutics, Inc.

CONTACT: Jennifer Neiman, Senior Manager, Corporate Communications,+1-720-540-5227, , or Derek Cole, Vice President, InvestorRelations, +1-720-540-5367, , both of Allos Therapeutics,Inc. jneiman@allos.com dcole@allos.com

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

Ticker Symbol: (NASDAQ-NMS:ALTH)

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