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Currently, no company worldwide has completed the required oral toxicity studies, metabolism studies, and long-term safety evaluations for GHK-Cu and submitted a GRAS notification to the FDA
relevant studies Read below for studies endorsing the use of GHK-Cu
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During the Phase 3 clinical trials, the percentages of patients with elevated HbA1c ( 6.5%) from baseline to Week 26 were 4.5% and 1.3% in the tesamorelin and placebo groups, respectively
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