US FDA approves new oral thalassemia drug; Dr Sanjeev Bagai calls it 'game changer'
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Donor availability and transplantation-related risks limit the broad use of allogeneic hematopoietic-cell transplantation in patients with transfusion-dependent β-thalassemia. Read more: http://www.nejm.org/doi/full/10.1056/NEJMoa1705342?query=featured_home | Blood and Hematology
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Donor availability and transplantation-related risks limit t…
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Gene therapy is emerging as a new-age treatment for thalassemia, offering hope beyond lifelong transfusions. In this approach, a patient’s own cells are taken and the faulty gene is corrected in two key ways—either through gene editing, or by using a vector/virus to introduce a healthy gene. Catch the full conversation in Hello Apollo – Our Care on Air Stay informed, because awareness is the first step toward better treatment choices. 🎧 Watch here: www.youtube.com/@apollohospitalsdelhi #Thalass
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A new gene therapy could be a game-changer for patients with severe anemia. The cost? $2.8 million.
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Key considerations when selecting patients with thalassemia or SCD for gene therapy
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