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8 13 The low prevalence was interpreted as a lag time in translating novel therapies into widespread clinical practice

It showed positive results in wounds and organ damage, even at low doses

No effects were seen when glucose was not administered, compatible with the idea that DPP-4 inhibition exerts an anti-hyperglycaemic effect by preventing degradation of endogenously released GLP-1 (26), subsequent studies in glucose-intolerant rodent models did show that the improved glycaemic control following in vivo DPP-4 inhibition was associated with enhanced intact GLP-1 responses to glucose challenges (2729)

Protocol: BPC-157 250 mcg daily SC + GHK-Cu topical or SC per dermatologic protocol