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

CJC-1295 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.

CJC-1295MK-677 (Ibutamoren)
CategoryPerformance & Growth HormonePerformance & Growth Hormone
Also known asCJC-1295 DAC, CJC-1295 without DAC (Mod GRF 1-29), Modified GRF 1-29Ibutamoren, Nutrobal, MK677, L-163,191
EvidenceResearch-stageResearch-stage
Dosing range100mcg–300mcg mcg, once daily (Mod GRF) or twice weekly (DAC version)10mg–50mg mg, once daily oral
AdministrationSubcutaneous injection (most common), Intramuscular injectionOral (capsule/liquid)
Key side effectsWater retention (especially early in protocol), Tingling or numbness in extremities, Injection site redness, Flushing (transient, shortly after injection)Water retention, Increased appetite, Elevated fasting glucose (long-term), Fatigue (initial, transient)
Cited sources2 references2 references

Key differences

  • Administration: CJC-1295 — Subcutaneous injection (most common), Intramuscular injection; MK-677 (Ibutamoren) — Oral (capsule/liquid).
  • Dosing units differ: CJC-1295 is dosed in mcg, MK-677 (Ibutamoren) in mg — they operate at different scales.
  • Frequency: CJC-1295 is typically once daily (Mod GRF) or twice weekly (DAC version); MK-677 (Ibutamoren) is once daily oral.

How each works

CJC-1295

Studies have demonstrated that CJC-1295 significantly increases plasma GH and IGF-1 levels. The DAC (Drug Affinity Complex) version extends the half-life to approximately 6–8 days via albumin binding, while Mod GRF 1-29 has a much shorter half-life (~30 minutes) and is dosed more acutely. Research in adults with GH deficiency has shown improved body composition and metabolic markers.

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 CJC-1295 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.