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FDA reschedules pixantrone and omacetaxine panel review

This article was originally published in Scrip

Executive Summary

The US FDA has rescheduled for March 22nd a meeting of the oncologic drugs advisory committee, which will review NDA submissions from Cell Therapeutics for pixantrone dimaleate (Pixuvri) in patients with non-Hodgkin's lymphoma (NHL) and ChemGenex Pharmaceuticals for omacetaxine mepesuccinate (Omapro) for patients with chronic myeloid leukaemia (CML).



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