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See Latest ArticlesPanel Will Consider Clinical Data Supporting Approval and Labeling
Genzyme, 08/31/09
Genzyme Corporation announced that its supplemental New Drug Application for Clolar will be discussed Tuesday, September at a public meeting of the FDA's Oncologic Drugs Advisory Committee in Silver Spring, Maryland. The panel is expected to consider the clinical trial results Genzyme submitted to support the approval and labeling of Clolar to treat older adult patients with acute myeloid leukemia, the most common type of acute leukemia in adults.
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