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Right in time: Mitapivat for the treatment of anemia in α- and β-thalassemia

Kuo and colleagues(1) evaluated the safety and efficacy of mitapivat, an oral pyruvate kinase activator, in adults with non-transfusion-dependent α-thalassemia or β-thalassemia. The high rate of hemoglobin response and good tolerability encourages further development in thalassemia.

Detalles Bibliográficos
Autores principales: Musallam, Khaled M., Taher, Ali T., Cappellini, Maria Domenica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9589095/
https://www.ncbi.nlm.nih.gov/pubmed/36260990
http://dx.doi.org/10.1016/j.xcrm.2022.100790