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The formulation succeeded in significantly reducing levels of CXCL-1 compared to placebo group [188]

A significant finding is its effect in pathological scarring models, such as keloids, where it promoted apoptosis in resistant fibroblasts and reduced cell proliferation during the G0/G1 phase of the cell cycle

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Depending on the GC selected, and the dosage administered, GC can remain in the body at levels high enough to result in an Adverse Analytical Finding (AAF) for days to weeks after administration