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The FDA approval process for peptides involves multiple phases

A 2025 regulatory analysis by Hurley and Frier at Frier Levitt outlined the practical implications: legitimate medical access to many peptides continues, but the sourcing pathway matters more than ever, and the clinician's knowledge of the current regulatory status of each specific compound is a prerequisite for appropriate prescribing

For instance, Drmic et al

Furthermore, since it shares structural similarities with HGH, it is less likely to cause immunogenic reactions, making it a promising treatment candidate that is safe to study

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