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Eisai says FDA approved new Dacogen dosing

Fri, 03/12/2010 - 2:17am
The Associated Press

Drugmaker Eisai Inc. said the Food and Drug Administration approved a new, longer dosing regimen of its bone marrow disease treatment Dacogen.

Eisai said the FDA cleared a five-day regimen of Dacogen as a treatment for myelodysplastic syndrome. The drug, which was developed through a partnership between SuperGen Inc. and MGI Pharma, was approved in May 2006 in a three-day dosing regimen. The new approval was announced late Thursday.

Myelodysplastic syndrome affects the production of blood cells.

The new regimen is intended for outpatient use: patients can get a larger dose of Dacogen once per day for five days, repeated once every four weeks. Previously the drug was given for three days. Each dose was given over a three-hour period, with eight-hour breaks between doses.

Eisai, a Japanese drugmaker, acquired MGI Pharma in early 2008. SuperGen is based in Dublin, Calif.

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