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Hodara R, Norris EH, Giasson BI, Mishizen-Eberz AJ, Lynch DR, Lee VM-Y, et al

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Key properties: Stimulates GH release from the pituitary (not the hypothalamus) Does not significantly raise cortisol or prolactin Short half-life (~2 hours) produces a sharp, pulsatile GH release Does not block somatostatin (the hormone that inhibits GH release) Selective for GH minimal effect on other hormones The selectivity is what makes ipamorelin the preferred GHRP for most protocols

Though, when the critical dosage limit of the basic measurement of around 1 to 1.5 mg/kg is given intravenously (IV) or 3 to 4 mg/kg, when given intramuscularly (IM), it is reached, the overdose symptoms can be shown up

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