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A randomized, placebo-controlled dose-finding trial found that PT-141 produced an increase in the number of satisfying sexual events per month when self-administered subcutaneously at doses of 0.75, 1.25, or 1.75 mg over 12 weeks (Clayton et al., 2016)

Unlike tesamorelin, ipamorelin has not been approved by the FDA for any use, and has yet to be reviewed in human clinical trials

If they persist beyond two weeks or severely limit daily function, inform your healthcare provider about dose adjustment options

GHK-Cu (targeted by GHK-Cu Cream) GHK-Cu plasma levels drop to approximately one-third of youthful levels by age 60