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Gene Therapy
Genome-Edited Cells for Sickle Cell Disease
Recruiting1 awardPhase 1
Memphis, Tennessee
This trial uses genetically modified blood stem cells from patients to treat Sickle Cell Disease. It works by reducing a gene's activity to increase beneficial fetal hemoglobin, aiming to lessen disease complications. The treatment involves a gene therapy that helps produce a type of hemoglobin that reduces the effects of the disease.
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