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US Food and Drug Administration Approval: Ruxolitinib for the Treatment of Patients with intermediate andhigh Risk Myelofibrosis

Deisseroth AB et al. – On November 16, 2011, Food and Drug Administration (FDA) granted full approval to ruxolitinib for the treatment of patients with intermediate or high risk myelofibrosis. This is the first drug approved for myelofibrosis (MF). [more...]

Clinical Cancer Research

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