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Aquavan (Fospropofol Disodium) Injection Data Presented at,Digestive Disease Week 2007

hat might cause MGI PHARMA's results to differ materially from those expressed or implied by such forward-looking statements include, but are not limited to, the ability of MGI PHARMA's product candidates to be proven safe and effective in humans, to receive marketing authorization from regulatory authorities, and to ultimately compete successfully with other therapies; continued sales of MGI PHARMA's marketed products; development or acquisition of additional products; reliance on contract manufacturing; changes in strategic alliances; continued access to capital; ability of MGI PHARMA to successfully complete the integration of Guilford with its existing operations; the risk that the perceived advantages of the Guilford transaction may not be achieved; and other risks and uncertainties detailed from time to time in MGI PHARMA's filings with the Securities and Exchange Commission including its most recently filed Form 10-Q or 10-K. MGI PHARMA undertakes no duty to update any of these forward-looking statements.

SOURCE: MGI PHARMA, INC.

Financial Dynamics
Robert Stanislaro, 212-850-5657
mgi@fd.com
or
Burson-Marsteller
Ryan McCormick, 312-596-3465
Email: ryan.mcormick@bm.com



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1. MGI Pharma Announces Positive Results from a Pivotal Phase 3 Study of Aquavan Injection in Patients Undergoing Bronchoscopy
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8. Genta Announces Results of Phase 1 Study Using Genasense Administered by Intermittent Subcutaneous Injection
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