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REVLIMID can also be accredited in the United States, Canada, Switzerland, Australia, New Zealand and several Latin American nations, as well as Malaysia and Israel, for transfusion-dependent anaemia due to low- or intermediate-1-danger myelodysplastic syndromes (MDS) related to a deletion 5q cytogenetic abnormality with or with out further cytogenetic abnormalities and in Europe for the treatment of sufferers with transfusion-dependent anemia as a consequence of low- or intermediate-1-threat MDS associated with an isolated deletion 5q cytogenetic abnormality when other therapeutic options are insufficient or inadequate.
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Fedratinib is intended to treat a bone marrow dysfunction generally known as myelofibrosis, and Celgene expects to file a brand new drug application with the FDA by the tip of 2018, with a marketing authorization software in the EU deliberate in 2019, in accordance with Chief Medical Officer Jay Backstrom.