MK-677 Reference
Educational, not medical advice reference for MK-677: GH Release; regulatory status, evidence posture, source review, and schedule notes. Also k…
Plain English
- What it is
- MK-677, also called ibutamoren, is a lab-made pill that nudges the body to release more of its own growth hormone and a linked growth signal called IGF-1. It is a small molecule, not a peptide, and not a hormone replacement. It is not approved by the FDA for any use; the maker tested it in people for years and then stopped its development.
- What people use it for
- It is the rare compound in this group that is taken by mouth instead of by injection, which is its main draw. People reach for it hoping for deeper sleep, higher IGF-1, more appetite, and gains in lean body mass.
- What the science shows
- Unlike most research compounds, MK-677 has real multi-year human trials in older adults. Those studies confirmed it raises growth hormone and IGF-1 and can add lean mass, but the gains did not turn into a clear health benefit, which is part of why it was never approved.
- The catch
- The same trials kept finding fluid buildup and swelling, higher fasting blood sugar, and lower insulin sensitivity. One study in elderly hip-fracture patients was stopped early over a heart-failure safety signal. It is also banned in sports by the World Anti-Doping Agency.
Reference summary
Multiple multi-year human trials in elderly sarcopenia and osteoporosis populations documented sustained increases in GH and IGF-1 with oral MK-677. Clinical benefit on lean mass and bone turnover was limited, and fluid retention and fasting glucose increases were consistent findings. No FDA approval followed.
Regulatory and posture
- Categories
- GH Release
- Aliases
- Ibutamoren, Ibutamoren mesylate, MK-0677, L-163,191, Oral ghrelin receptor agonist (non-peptide)
- Evidence posture
- human - Large human trials exist, but development was discontinued. Water retention and raised fasting glucose are consistently reported; a congestive-heart-failure signal was reported in one elderly hip-fracture trial.
- Regulatory status
- Investigational non-peptide ghrelin-receptor agonist. Merck discontinued development after trials for sarcopenia and osteoporosis did not reach approval. There is no FDA-approved MK-677 drug label. MK-677 is an orally active small molecule, not a peptide, but is commonly grouped with peptide GH secretagogues. A September 18, 2024 FDA Federal Register notice (document 2024-21241) listed ibutamoren mesylate among bulk drug substances the Pharmacy Compounding Advisory Committee considered for inclusion on the section 503A Bulks List; this nomination review is not an approval, and MK-677 remains not FDA-approved.
- Content review status
- research reference
Selected public sources
- PubMed: MK-677 (ibutamoren) reverses diet-induced catabolism, healthy adults (Murphy 1998, JCEM)
- PubMed: Nass 2008 MK-677 body-composition and clinical-outcomes RCT in healthy older adults (Ann Intern Med)
- PubMed: Adunsky 2011 MK-0677 hip-fracture Phase IIb RCT (Arch Gerontol Geriatr)
- FDA Federal Register notice (Sept 18, 2024): Pharmacy Compounding Advisory Committee considered ibutamoren mesylate, ipamorelin, and kisspeptin-10 for the 503A Bulks List
Related tools
- Protocol builder overview - Public overview of the Pro protocol builder.
For research and educational purposes only. Not medical advice.