| CPC A61K 35/545 (2013.01) [A61K 35/28 (2013.01); A61K 35/33 (2013.01); A61K 35/38 (2013.01); A61K 35/50 (2013.01); A61K 35/51 (2013.01); A61K 40/10 (2025.01); A61K 40/40 (2025.01); A61K 40/414 (2025.01); A61K 45/06 (2013.01); A61P 25/28 (2018.01); A61K 2035/124 (2013.01); A61K 2239/31 (2023.05); A61K 2239/38 (2023.05)] | 16 Claims |
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1. A method of treating a brain disease, disorder or a symptom thereof in a human patient in need of such treatment comprising administering a pharmaceutical composition to the patient, the pharmaceutical composition comprising about 5×105 to 5×109 human CD34+ stem cells, wherein the human stem cells are enriched with functional human exogenous mitochondria, wherein the brain disease or disorder is not a primary mitochondrial disease or disorder caused by a pathogenic mutation in mitochondrial DNA or by a pathogenic mutation in nuclear DNA encoding a mitochondrial protein; and wherein the disease or disorder is selected from the group consisting of Parkinson Disease (PD), Alzheimer Disease (AD), adrenoleukodystrophy (ALD), Huntington Disease (HD), Guillain Barre Syndrome (GBS), and autism.
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