⚠️ Research Use Only — Compounds discussed are research chemicals, not FDA-approved for human use. Not medical advice. Full disclaimers →
Also known as: Ibutamoren, Ibutamoren Mesylate, L-163,191, Nutrobal
MK-677 is a gh secretagogue (oral) research compound (not FDA-approved for human use) studied for sustained gh/igf-1 elevation. MK-677 (Ibutamoren) is an orally bioavailable growth hormone secretagogue studied for sustainably elevating GH and IGF-1 levels over 24 hours with a single daily pill. Research dose: 12.50–12.50 mg 7x/wk. Half-life: 1 days. Available from COA-verified vendors with code PEPTIDEX for up to 20% off.
Sourcing data for MK-677 is updating.
We verify new listings weekly — check back soon.
Sourcing data for MK-677 is updating.
We verify new listings weekly — check back soon.
Non-peptide ghrelin receptor (GHSR1a) agonist that stimulates prolonged, pulsatile growth hormone release from the pituitary gland. Unlike injectable GH peptides, MK-677 is orally bioavailable with a
COA-verified vendors · Use code PEPTIDEX for up to 20% off
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Compare All VendorsNon-peptide ghrelin receptor (GHSR1a) agonist that stimulates prolonged, pulsatile growth hormone release from the pituitary gland. Unlike injectable GH peptides, MK-677 is orally bioavailable with a ~24-hour half-life, enabling once-daily dosing. Increases IGF-1 levels for up to 12 months without desensitization of the GH axis. Does not suppress natural GH secretion patterns or affect cortisol levels at standard doses.
Chapman et al. (J. Clin. Endocrinol. Metab.): 25mg daily MK-677 for 2 weeks in healthy elderly subjects restored IGF-1 and GH profiles to young adult levels without altering cortisol, prolactin, insulin, or thyroid hormones.
ModerateNass et al. (J. Clin. Endocrinol. Metab.): 2-year RCT in 65 healthy elderly adults. 25mg/day MK-677 increased GH and IGF-1 to young adult levels, increased fat-free mass by ~1.1kg, and did not affect BMD. Notable: fasting glucose increased by ~0.3 mmol/L.
StrongSvensson et al. (J. Clin. Endocrinol. Metab.): 8-week RCT in obese males. 25mg/day MK-677 significantly increased GH secretion, IGF-1, and fat-free mass. Transient increase in appetite and mild insulin resistance noted.
ModerateMurphy et al. (J. Clin. Endocrinol. Metab.): MK-677 reversed diet-induced nitrogen wasting in healthy young volunteers on caloric restriction, demonstrating potent anti-catabolic properties.
ModerateCopinschi et al. (Neuroendocrinology): MK-677 increased duration of stage IV (deep) sleep by 50% and REM sleep by 20% in both young and older subjects, correlating with enhanced overnight GH secretion.
ModerateMurphy et al. (J. Clin. Endocrinol. Metab.): 12-month study in postmenopausal women showing MK-677 (25mg/day) increased osteocalcin and bone-specific alkaline phosphatase, suggesting improved bone formation.
ModerateA study published in Annals of medicine investigating the effects and mechanisms.
ModerateA study published in Recent progress in hormone research investigating the effects and mechanisms.
PreclinicalA study published in The Journal of clinical endocrinology and metabolism investigating the effects and mechanisms.
PreclinicalA study published in Annales d'endocrinologie investigating the effects and mechanisms.
PreclinicalOral GH secretagogue with extensive clinical data (2+ year RCTs). Key concern: impairs insulin sensitivity and raises fasting glucose, especially in elderly/obese populations. One hip fracture trial in elderly was stopped early due to CHF signals. WADA prohibited. Not FDA-approved. Use caution in pre-diabetic or insulin-resistant individuals.
See our evidence grading methodology for how we evaluate and grade peptide safety data.
* Dosing data from published literature — not a human use recommendation.
Standard dose: 10-25mg once daily. Oral capsule or liquid. Start at 10mg to assess appetite increase and glucose response. Pre-bed dosing leverages natural GH pulse. 5-on/2-off cycles used to manage appetite and insulin sensitivity.
Week 1
Significant appetite increase; deeper sleep onset; vivid dreams; mild water retention
Weeks 2–4
Sustained IGF-1 elevation confirmed on bloodwork; improved recovery; skin quality improvement; morning puffiness from water retention
Month 2–3
Measurable fat-free mass increase (~1-2 lbs); improved bone turnover markers; hair/nail growth acceleration; monitor fasting glucose
Long-term
2-year clinical data shows sustained IGF-1 without tachyphylaxis; continued body composition benefits; requires ongoing glucose monitoring
| Side Effect | Incidence | Severity |
|---|---|---|
Increased appetite Most pronounced in first 2-4 weeks; often the dose-limiting factor | ~40-60% of users | moderate |
Water retention / bloating Mainly facial/periorbital puffiness; dose-dependent | ~30% of users | moderate |
Insulin resistance / elevated fasting glucose Monitor HbA1c and fasting glucose; more pronounced in obese/elderly | ~15-25% of users | moderate |
Lethargy / drowsiness Mitigated by pre-bed dosing | ~15% of users | mild |
Numbness / tingling (paresthesia) | ~8% of users | mild |
Joint pain Related to rapid GH/IGF-1 elevation; usually transient | ~5% of users | mild |
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⚠️ Educational only · Not medical advice · For research use only. Information on this page is compiled from peer-reviewed literature and is intended strictly for educational and informational purposes. Peptides discussed may be unapproved research chemicals — consult a licensed healthcare professional before considering any peptide compound. Read our full disclaimer
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