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Motixafortide successfully mobilized stem cells in 90% of sickle cell patients, including those who failed prior treatment, advancing gene therapy access.
Ayrmid, Ltd. reported at the 2025 American Society of Hematology Annual Meeting that motixafortide, a long-acting CXCR4 inhibitor, successfully mobilized enough hematopoietic stem cells in 90% of 10 sickle cell disease patients for gene therapy, including 86% of those who previously failed plerixafor.
Two patients have undergone successful transplants, and manufacturing continues for others.
The findings suggest motixafortide could overcome a major barrier to gene therapy access, potentially expanding treatment eligibility.
It is already FDA-approved for multiple myeloma but not yet for sickle cell disease.
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Motixafortide movilizó con éxito las células madre en el 90% de los pacientes con células falciformes, incluidos los que habían fracasado en el tratamiento previo, lo que permitió el acceso a la terapia génica.