Tuesday, October 6, 2009

Genzyme Receives FDA Complete Response Letter for Clolar

Oct 6, 2009 - Genzyme Corporation announced today that the FDA provided a complete response letter regarding the company's supplemental New Drug Application for Clolar® (clofarabine) in previously untreated older adult patients with acute myeloid leukemia (AML) and at least one unfavorable baseline prognostic factor.

the details can be read here.

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