Editas Medicine Announces Breakthrough in In Vivo Gene Editing for Sickle Cell Disease and Beta Thalassemia at European Hematology Association 2025 Congress

Reuters
12 Jun
Editas Medicine Announces Breakthrough in In Vivo Gene Editing for Sickle Cell Disease and Beta Thalassemia at European Hematology Association 2025 Congress

Editas Medicine, Inc., a leading gene editing company, has announced the presentation of new in vivo data at the European Hematology Association 2025 Congress. The data demonstrates therapeutically relevant levels of HBG1/2 promoter editing in hematopoietic stem cells using a single dose of proprietary targeted lipid nanoparticle delivery in non-human primates. This approach, which aims to upregulate fetal hemoglobin, is in pre-clinical development for treating sickle cell disease and beta thalassemia. The results, which achieved a 58% mean editing rate at five months post-treatment, will be detailed in a poster session scheduled for June 14, 2025, at the Allianz MiCo, Milano Convention Centre. A presentation of these findings is currently available on the Editas Medicine website.

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