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

MK-677 (Ibutamoren) vs Mod-GRF(1-29)

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.

MK-677 (Ibutamoren)Mod-GRF(1-29)
CategoryPerformance & Growth HormonePerformance & Growth Hormone
Also known asIbutamoren, Nutrobal, MK677, L-163,191Modified GRF(1-29), CJC-1295 without DAC, Tetrasubstituted GRF, Sermorelin analog
EvidenceResearch-stageResearch-stage
Dosing range10mg–50mg mg, once daily oral100mcg–200mcg mcg, 2–3x daily, co-administered with a GHRP (pre-sleep, pre-workout, and/or upon waking)
AdministrationOral (capsule/liquid)Subcutaneous injection, Intramuscular injection
Key side effectsWater retention, Increased appetite, Elevated fasting glucose (long-term), Fatigue (initial, transient)Water retention (mild, dose-dependent), Tingling / numbness in extremities (carpal tunnel-like at high doses), Increased appetite (via GHRP component — less with Mod-GRF alone), Flushing or warmth at injection site
Cited sources2 references2 references

Key differences

  • Administration: MK-677 (Ibutamoren) — Oral (capsule/liquid); Mod-GRF(1-29) — Subcutaneous injection, Intramuscular injection.
  • Dosing units differ: MK-677 (Ibutamoren) is dosed in mg, Mod-GRF(1-29) in mcg — they operate at different scales.
  • Frequency: MK-677 (Ibutamoren) is typically once daily oral; Mod-GRF(1-29) is 2–3x daily, co-administered with a GHRP (pre-sleep, pre-workout, and/or upon waking).

How each works

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.

Mod-GRF(1-29)

Native GHRH(1-29) is rapidly cleaved by plasma dipeptidyl peptidase IV (DPP-IV) within 2–3 minutes. Mod-GRF(1-29) incorporates four amino acid substitutions (positions 2, 8, 15, 27) that resist DPP-IV degradation, extending the half-life to approximately 30 minutes while preserving GHRH receptor binding affinity. This creates a half-life window aligned with physiological GH pulsatility, making it suitable for 2–3x daily injections that mimic natural GH release patterns.

Read the full MK-677 (Ibutamoren) profileRead the full Mod-GRF(1-29) 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.