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Discussion 1) At the end of the trial it was recorded that 100-102 participants received an active dose of cagrilintide, 99 participants were administered a 3.0 mg dose of liraglutide and 101 participants were given volume-matched placebo

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GHK-Cu Dosing in Research Models Research dosing of GHK-Cu varies significantly by application area: Topical research formulations typically reported in % w/w of finished formulation (0.05-2%)

Gastrointestinal adverse events including nausea and vomiting were the most common side effects but were generally transient and mild to moderate in severity

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