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Research shows GHK-Cu's therapeutic dose is approximately 300-fold below its toxic threshold

Oncogenesis 7 , 8 (2018)

Differential expression of HSPA1 and HSPA2 proteins in human tissues

They are provided to help interpret the literature, not as a protocol for human use, and cagrilintide in particular has no approved dose for any application

The compound has been found to operate in the postrema and nucleus of the hindbrain solitary tract in order to both induce satiety and regulate appetite by acting on receptors found in the laterodorsal tegmental nucleus, ventral tegmental area, and the hypothalamus [1]

It also functions as an antioxidant by delivering non-toxic bioavailable copper to cells while preventing free radical activity from unbound ionic copper