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This study evaluated the therapeutic potential of non-gene-edited human chemically induced pluripotent stem cell-derived neural stem cells (hCiPSC-NSCs) in a prenatal valproic acid (VPA)-induced rat model of ASD, using a dual-pathway administration strategy (intravenous systemic delivery combined with an intracerebroventricular boost)

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BPC-157 has been shown in research settings to influence angiogenic signaling, nitric oxide pathways, and fibroblast activity, while TB-500 has been studied for its role in actin regulation, cell migration, and wound-healing mechanisms