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Preclinical Toxicology: Toxicity studies in rodents indicate that even high doses (e.g., 20 mg/kg) do not result in gross organ toxicity or lethality in the acute setting

Its design pairs a stabilised growth-hormone-releasing hormone (GHRH) analog with a selective ghrelin-receptor (growth hormone secretagogue receptor, GHS-R) agonist, engaging two distinct upstream signalling pathways that converge at the somatotroph cell on enhanced GH release

This prolonged stimulation often leads to greater gains in lean muscle mass, fat reduction, and improved recovery

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