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The ODAC meeting was planned two New Drug Applications, outputted from those brought the application by ChemGenex to OMAPRO was public counseling session of 10 February 2010 plan was suspended due to extreme weather Service Washington DC omacetaxine mepesuccinate) for treatment of adult patients with chronic myeloid leukemia , to. Do not against therapy with imatinib and that Bcr-Abl T315I mutation of developing ChemGenex the NDA on the 9 September 2009. The NDA came approved by the FDA on 10 Assumed November 2009 granted priority review status.

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ChemGenex believe in safety and efficacy of OMAPRO for the treatment of patients with chronic myeloid leukemia , which is resistant to imatinib and which Bcr-Abl T315I mutations. The company faced up to question FDA and we are confident our ability to answered these issues during ODAC meeting. OMAPRO depends a considerable unmet needs of patients with of the T315I mutation, a marker is for the resistance towards tyrosine kinase inhibitors, who currently have no effective treatment option and is often a bad prognosis.