MK-677
Ibutamoren · MK-0677
Ghrelin-receptor agonism underlies MK-677’s role in growth hormone-axis investigations.
Not medical advice. Educational reference only.
- Typical dose
- Oral: 10–25 mg daily; separate subcutaneous research schedules: 100 mcg once daily, 200 mcg twice daily or 300 mcg 3x daily
- Route
- Oral; Subcutaneous injection
- Storage
- Keep at 2–8°C after mixing and use within 28 days.
What is MK-677?
MK-677 activates the ghrelin receptor and is used orally in research on the growth hormone axis. It is also called ibutamoren. It has no FDA approval.
Mechanism of action
Ghrelin-receptor agonism underlies MK-677’s role in growth hormone-axis investigations.
Targets: Ghrelin receptor
Research indications
Growth Hormone Support
Most effectivePituitary signaling promotes release of the body’s own growth hormone.
Body Composition
EffectivePotential changes include greater lean mass and lower amounts of body fat.
Recovery & Repair
EffectiveResearch examines tissue restoration and recovery following injury or exercise.
Sleep Quality
ModerateSome research schedules are associated with better restorative and slow-wave sleep.
Research protocols
These are commonly discussed research protocols — not medical advice. Consult a healthcare provider before use.
| Goal | Amount | Frequency | Route |
|---|---|---|---|
| Starting | 100 mcg | Once daily | Subcutaneous injection |
| Standard | 200 mcg | Twice daily | Subcutaneous injection |
| Maximum | 300 mcg | 3x daily | Subcutaneous injection |
Interactions
Insulin / IGF-1
MonitorCorticosteroids
CautionThyroid Hormones
MonitorBPC-157
CompatibleTB-500
CompatibleIpamorelin + CJC-1295
CompatibleSomatostatin Analogs
Avoid
How to reconstitute and inject
Diluent: Use bacteriostatic water; avoid saline because precipitation may occur.
- Let the refrigerated vial stand at room temperature for 15–20 minutes before preparation.
- Disinfect the stopper using an alcohol swab, then wait until it has dried fully in the air.
- Measure the calculated quantity of bacteriostatic water with a sterile syringe. Use only this diluent; avoid saline because precipitation may occur.
- Add the water gradually against the inner vial wall. Keep the stream away from the powder itself.
- Rotate the vial with a gentle swirling motion. Do not shake forcefully, because this can degrade the contents.
- Wait 2–3 minutes for the powder to dissolve completely, and check that the liquid is transparent and has no color.
- Use an insulin syringe to withdraw the calculated amount for injection beneath the skin.
- Inject in the thigh, abdomen or upper arm. Change the injection location each time to help prevent lipodystrophy.
- Refrigerate the mixed solution at 2–8°C. Use it within a maximum of 28 days after preparation.
What to expect
- Week 1–2
- Sleep may improve during weeks 1–2, although mild fluid retention can occur at the beginning.
- Week 2–4
- During weeks 2–4, sleep may become deeper and recovery improve; a modest appetite increase is possible.
- Week 4–8
- Weeks 4–8 may bring noticeable changes in energy, body composition and the speed of recovery.
- Week 8–12
- During weeks 8–12, skin changes may become evident alongside lower body fat and more lean tissue.
- Week 12+
- After week 12, gains in strength, body composition and general vitality may persist. These are research expectations, not assured outcomes.
Side effects and safety
- Fluid retention with mild bloating, particularly at initiation
- Greater appetite, especially with GHRP compounds
- Warmth or flushing around the injection location
- Numbness or tingling resembling carpal tunnel symptoms with larger doses
- Lethargy or fatigue when dosing times are unsuitable
- Possible increases in prolactin and cortisol, particularly with GHRP-6
- Raised blood glucose; monitor if you have diabetes or prediabetes · Rare
MK-677: not approved in the US.
Regulatory status
US
Not approvedFDA: no approval for human treatment; research use only. No 503A ban is identified; compounding authorization remains unknown. Telehealth is not applicable.
- Rx required
- No
- Telehealth
- N/A
Frequently asked questions
What is MK-677?
It is an unapproved compound studied for growth hormone signaling.
Which benefits are being investigated?
Research concerns GH release, lean mass, recovery and sleep.
Which dosing schedules are discussed?
The oral research range is 10–25 mg daily, with an approximate half-life of 24 hours. The separate subcutaneous schedules use 100, 200 or 300 mcg; they do not establish an oral-equivalent dose or a validated injectable regimen.
What safety issues matter?
Secretagogues may cause fluid retention, appetite changes, tingling and fatigue. Cortisol and prolactin responses vary.
References
MK-677, an orally active growth hormone secretagogue: effects on body composition (1998)
Two-year treatment with ibutamoren increases bone mineral density, body composition, and quality of life (2008)
MK-677, an orally active growth hormone secretagogue, reverses diet-induced catabolism. (1998)
Characterization of growth hormone secretagogue small molecule ibutamoren (MK-0677) and its possible metabolites in thoroughbred horses for doping control. (2022)
Ibutamoren (MK-677) studies on ClinicalTrials.gov (2024)