For informational and research purposes only. Not medical advice. Content is aggregated from public sources. Always consult a qualified healthcare provider.
Performance & Growth Hormone · Comparison

ACE-031 vs MK-677 (Ibutamoren)

A neutral, side-by-side comparison of two performance & growth hormone peptides — their mechanisms, dosing ranges, administration routes, side effects, and research evidence. For research and educational purposes only.

ACE-031MK-677 (Ibutamoren)
CategoryPerformance & Growth HormonePerformance & Growth Hormone
Also known asACVR2B-Fc, ActRIIB-Fc fusion proteinIbutamoren, Nutrobal, MK677, L-163,191
EvidenceInvestigational (in trials)Research-stage
Dosing range0.3mg/kg–3mg/kg mg/kg, every 2–4 weeks (subcutaneous injection)10mg–50mg mg, once daily oral
AdministrationSubcutaneous injectionOral (capsule/liquid)
Key side effectsNosebleeds (epistaxis — most common reported AE), Telangiectasia (visible small blood vessel dilation), Gum bleeding, Elevated hemoglobinWater retention, Increased appetite, Elevated fasting glucose (long-term), Fatigue (initial, transient)
Cited sources2 references2 references

Key differences

  • Evidence level differs: ACE-031 is investigational (in trials), while MK-677 (Ibutamoren) is research-stage.
  • Administration: ACE-031 — Subcutaneous injection; MK-677 (Ibutamoren) — Oral (capsule/liquid).
  • Dosing units differ: ACE-031 is dosed in mg/kg, MK-677 (Ibutamoren) in mg — they operate at different scales.
  • Frequency: ACE-031 is typically every 2–4 weeks (subcutaneous injection); MK-677 (Ibutamoren) is once daily oral.

How each works

ACE-031

ACE-031 functions as a decoy receptor, binding myostatin, activin A/B, GDF-11, and BMP-9 in circulation before they can activate cellular ActRIIB receptors. In the Duchenne muscular dystrophy Phase 2 trial, ACE-031 produced meaningful lean body mass increases but was halted due to vascular side effects (epistaxis, telangiectasia) requiring dose and safety optimization.

MK-677 (Ibutamoren)

MK-677 binds the ghrelin receptor (GHS-R1a) to stimulate pulsatile GH release and increase circulating IGF-1. Unlike peptide GHRPs it survives oral administration. Clinical trials demonstrate significant increases in GH pulsatility and IGF-1 without suppression of the endogenous GH axis, though long-term use raises glucose metabolism concerns.

Read the full ACE-031 profileRead the full MK-677 (Ibutamoren) profile

This comparison aggregates public research and structured profile data for informational purposes only. It is not medical advice and does not recommend either compound for human use. Consult a qualified healthcare provider before considering any peptide.