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 Tesamorelin

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)Tesamorelin
CategoryPerformance & Growth HormonePerformance & Growth Hormone
Also known asIbutamoren, Nutrobal, MK677, L-163,191Egrifta, Egrifta SV, TH9507, GHRH analog
EvidenceResearch-stageFDA-approved
Dosing range10mg–50mg mg, once daily oral1.28mg–2mg mg, once daily (subcutaneous)
AdministrationOral (capsule/liquid)Subcutaneous injection (abdomen, with site rotation)
Key side effectsWater retention, Increased appetite, Elevated fasting glucose (long-term), Fatigue (initial, transient)Injection site reactions (erythema, pruritus), Peripheral edema, Arthralgia (joint pain), Myalgia
Cited sources2 references5 references

Key differences

  • Evidence level differs: MK-677 (Ibutamoren) is research-stage, while Tesamorelin is fda-approved.
  • Administration: MK-677 (Ibutamoren) — Oral (capsule/liquid); Tesamorelin — Subcutaneous injection (abdomen, with site rotation).
  • Frequency: MK-677 (Ibutamoren) is typically once daily oral; Tesamorelin is once daily (subcutaneous).
  • Research depth: this profile cites 2 sources for MK-677 (Ibutamoren) vs 5 for Tesamorelin.

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.

Tesamorelin

Tesamorelin stimulates pulsatile growth hormone (GH) release from the pituitary, raising serum IGF-1 and preferentially reducing visceral adipose tissue (VAT). FDA-registration trials (Falutz et al., NEJM 2007; JAIDS 2010) showed ~15% VAT reduction versus placebo over 26 weeks. Later randomized trials (Stanley et al., JAMA 2014; Lancet HIV 2019) extended the evidence to liver fat, showing meaningful reductions in hepatic fat fraction and attenuated fibrosis progression in HIV-associated NAFLD.

Read the full MK-677 (Ibutamoren) profileRead the full Tesamorelin 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.