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» Synribo Clears FDA Hurdle, Gains Nod in CML Patients
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Synribo Clears FDA Hurdle, Gains Nod in CML Patients
Oct. 29, 2012
By
Jennifer Boggs
Three years after a new drug application was first submitted for leukemia drug omacetaxine mepesuccinate, during which the product moved twice into different hands via M&A transactions, the FDA granted a long-awaited nod Friday.
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