MK-677
Overview
MK-677, also known as ibutamoren, is an orally active, non-peptide agonist of the ghrelin receptor. Its oral bioavailability distinguishes it from injectable growth-hormone secretagogues and gives it a research-friendly profile as a tool compound in growth-hormone-axis studies.
MK-677 has been studied for its activity at the ghrelin, or growth-hormone-secretagogue, receptor (GHS-R1a), where it is characterized for stimulating pulsatile growth-hormone release and raising IGF-1. It has been investigated in clinical trials in contexts such as growth-hormone deficiency, frailty, and catabolic states, although it is not an approved drug and those studies do not establish sex-specific regimens.
What makes MK-677 notable for a performance and endocrine catalog is the combination of an oral route with a defined secretagogue mechanism. Some of its trials included women; our evidence review tracks how many of the underlying studies reported outcomes by sex, an open research question at this stage.
Summary
MK-677 (ibutamoren) is an orally active ghrelin-receptor agonist that raises growth hormone and IGF-1. It has been investigated in clinical trials, for growth-hormone deficiency, frailty, and catabolic states, but is not an approved drug. Some of those trials included women; none establish female-specific dosing.
Evidence in women
Mechanism
Agonist at the ghrelin / growth-hormone-secretagogue receptor (GHS-R1a). Stimulates pulsatile GH release and raises IGF-1, with the practical distinction of oral bioavailability.
Free research guide
How to tell real female data from male-extrapolated claims, with the questions to ask about any compound.
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Educational information for laboratory and research use only. Not medical advice, a recommendation, or a claim of safety or efficacy; no personal dosing. “Unstudied” means no qualifying study was found, not that a compound is safe or unsafe.