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The model was first fitted to the training concentrations (37.5 and 25 M doxorubicin), and then used to simulate the test concentrations (50, 12.5 and 10 M doxorubicin) as a means of blind validation, showing good accordance between the experimental and in silico outputs for all concentrations of doxorubicin

The pharmacokinetic groundwork that is also missing Even before an efficacy trial, injectable GHK-Cu lacks the basic human pharmacokinetic characterization that any injectable drug candidate would require: measured plasma half-life of the intact complex, the fraction of administered copper that binds to plasma proteins versus remains peptide-bound, tissue distribution, and how much functional complex if any actually reaches the dermis

10.1016/j.theriogenology.2018.12.017 28

Compounded medications such as MIC + B12 are not FDA approved

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