Reblozyl first and only erythroid maturation agent to be approved in the EU

27 June 2020

The European Commission (EC) on Friday approved Reblozyl (luspatercept), developed by Celgene, which is now part of US pharma major Bristol-Myers Squibb (NYSE: BMY) under a $74 billion buy-out that completed in November 2019, and Acceleron Pharma (Nasdaq: XLRN).

Reblozyl is cleared in the European Union for the treatment of:

Adult patients with transfusion-dependent anemia due to very low-, low- and intermediate-risk myelodysplastic syndromes (MDS) with ring sideroblasts, who had an unsatisfactory response or are ineligible for erythropoietin-based therapy.
Adult patients with transfusion-dependent anemia associated with beta thalassemia.

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