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FDA Approves Five-Day Dosing Regimen for Dacogen(R) (decitabine) for Injection, Offering a New Outpatient Dosing Option for Myelodysplastic Syndromes (MDS)
Date:3/11/2010

ED QUOTE

"We are very pleased that the FDA has granted approval of the alternate five-day dosing regimen for Dacogen (decitabine) for Injection," said Kathy Heptinstall, operating director, The MDS Foundation, Inc.  "This increases dosing options and provides alternatives for our MDS patients, particularly those who are being treated in the outpatient setting."  

For media inquiries, contact Kathy Heptinstall, operating director, The MDS Foundation, Inc. at 1-800-MDS-0839, outside the U.S. only (609) 298-6746; fax (609) 298-0590.

SOURCE Eisai Inc.

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