Long-term safety and erythroid response with luspatercept treatment in patients with β-thalassemia
Background: β-thalassemia is a hereditary blood disorder resulting in ineffective erythropoiesis and anemia. Management of anemia with regular blood transfusions is associated with complications including iron overload. Here, we report long-term safety and efficacy results of the first clinical stud...
Main Authors: | , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
SAGE Publishing
2022-12-01
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Series: | Therapeutic Advances in Hematology |
Online Access: | https://doi.org/10.1177/20406207221134404 |