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An investigational cell therapy regimen developed by Bundang CHA Hospital for the treatment of subacute stroke. The therapy consists of allogeneic umbilical cord blood (UCB) cells, matched for human leukocyte antigens (HLA-A, B, and DR) and sourced from the CHA Cord Blood Bank. In clinical development (e.g., NCT04013646), the UCB infusion is administered as a single intravenous dose, often in combination with recombinant human erythropoietin (rhEPO) to enhance therapeutic outcomes. The biological mechanism involves the neuroprotective, neuroregenerative, and anti-inflammatory properties of the cord blood cells, while the erythropoietin component is intended to synergistically promote angiogenesis and neurogenesis via the erythropoietin receptor. The treatment is targeted at patients in the subacute phase of stroke, typically one to nine months post-onset, to facilitate neurological recovery and functional improvement.
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