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its derivative PT-141 (Bremelanotide) was FDA approved in 2019 as Vyleesi (HSDD in women)
Reference: In Silico Pharmacogenomic Assessment of Glucagon-like Peptide-1 (GLP1) Agonists and the Genetic Addiction Risk Score (GARS) Related Pathways: Implications for Suicidal Ideation and Substance Use Disorder by Alireza Sharafshah, Kai-Uwe Lewandrowski, Mark S
In practice, an exploratory therapeutic trial of 10002000 mg EPA/DHA daily for at least 8 weeks could be considered, and personalised based on testing of the O3I
GHK-Cu is not a controlled substance in the UK and can be legally supplied for laboratory research purposes only
Patent number 4,602,039 *These statements have not been evaluated by the Food & Drug Administration
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