Bristol Myers Squibb announced the Committee for Medicinal Products for Human Use of the European Medicines Agency has recommended approval of Reblozyl as a treatment for adult patients with transfusion-dependent anemia due to very low, low and intermediate-risk myelodysplastic syndromes. The recommendation will now be reviewed by the European Commission, which has the authority to approve medicines for the European Union. Upon approval, this would represent the fourth authorized indication for Reblozyl in the EU.
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