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Reported Limitations and Considerations in GHK-Cu Research Gaps in the Current Evidence Base Despite a substantial pre-clinical record, GHK-Cu lacks large-scale human clinical trial data for most reported applications

Suspected adverse reactions should be reported through the MHRA Yellow Card scheme (yellowcard.mhra.gov.uk)

A significant decrease in the levels of T3 and T4 has been recorded after 30 days of TBT administration when compared with both the control and the TBT+ GTE groups (Tables 1 and 2)

Warnings Do not exceed the stated daily dose

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Prophylaxis and treatment of other macrocytic anaemias associated with Vitamin B12 deficiency