Profile of Luspatercept in the Treatment of Anemia in Adults with Non-Transfusion-Dependent β-Thalassemia (NTDT): Design, Development and Potential Place in Therapy.

Khaled M Musallam, Ali T Taher, Antonis Kattamis, Maria Domenica Cappellini, Kevin H M Kuo, Sujit Sheth

Journal: Drug design, development and therapy 2023;17():1583-1591

PMID: 37255740

Abstract

Over the past decade, evidence has been mounting on the detrimental clinical sequelae of untreated anemia in patients with non-transfusion-dependent β-thalassemia (NTDT). There are no pharmacologic agents that are specifically approved for the management of anemia in NTDT, and available options such as splenectomy, transfusion therapy, and hydroxyurea each come with their own shortcomings, especially for long-term use. Luspatercept is an erythroid maturation agent that has been evaluated in a Phase 2, randomized trial and showed a significant benefit in raising hemoglobin level by at least 1 g/dL in adults with NTDT and a baseline hemoglobin level ≤10 g/dL. These data led to luspatercept's approval by the European Commission for the treatment of anemia in adults with NTDT and presents the first evidence-based approach for a novel agent that is able to ameliorate anemia in this patient population.

© 2023 Musallam et al.

Address: Thalassemia Center, Burjeel Medical City, Abu Dhabi, United Arab Emirates.; Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon.; First Department of Pediatrics, National and Kapodistrian University of Athens, Athens, Greece.; Division of Hematology, University of Toronto, Toronto, ON, Canada.; Division of Hematology and Oncology, Department of Pediatrics, Weill Cornell Medicine, New York, NY, USA.; Department of Clinical Sciences and Community, University of Milan, Ca' Granda Foundation IRCCS Maggiore Policlinico Hospital, Milan, Italy.
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