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Autologous umbilical cord blood mononuclear cells is an investigational cell therapy developed by The University of Texas Health Science Center at Houston (UTHealth Houston) for the treatment of hypoxic neurologic injury in infants with high-risk congenital diaphragmatic hernia (CDH). The therapy consists of mononuclear cells isolated from the patient's own umbilical cord blood collected at birth. It is administered intravenously in four doses over the first week of life. These cells are hypothesized to mitigate brain injury by modulating the inflammatory response and promoting neuroprotection and repair mechanisms. This biologic therapy is currently being evaluated in a Phase 1 clinical trial at Children's Memorial Hermann Hospital to determine its safety and potential to improve neurological and neurodevelopmental outcomes in this high-risk population, which currently lacks approved neuroprotective treatments.
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