ASH 2023 | Improving outcomes for hemophilia patients through the implementation of gene therapies
Evelien Krumb
• 12 Dec 2023
In recent years, notable progress in gene therapy for hemophilia has led to FDA approvals. In this video, Evelien Krumb, MD, UCLouvain Saint-Luc, Brussels, Belgium, discusses how gene therapy can potentially eliminate bleeding episodes, avoiding the need for regular treatments and alleviating the psychological burden of living with hemophilia. This interview took place at the 65th ASH Annual Meeting and Exposition, held in San Diego, CA.
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Disclosures
Research Funding: Swedish Orphan Biovitrum (Sobi), CSL Behring
Honoraria: BioMarin
