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Carey et al

(1998, Eur J Endocrinol) as a GHS-R1a agonist with GH-release potency comparable to GHRP-6 but without the ACTH, cortisol or prolactin elevation that limits other secretagogues

You will also find out about the possible side effects

However, Hagen and Jones reported an increase in plasma glutathione levels in four out of five subjects after a single oral dose of 15 mg/kg body weight