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 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.

ACE-031Tesamorelin
CategoryPerformance & Growth HormonePerformance & Growth Hormone
Also known asACVR2B-Fc, ActRIIB-Fc fusion proteinEgrifta, Egrifta SV, TH9507, GHRH analog
EvidenceInvestigational (in trials)FDA-approved
Dosing range0.3mg/kg–3mg/kg mg/kg, every 2–4 weeks (subcutaneous injection)1.28mg–2mg mg, once daily (subcutaneous)
AdministrationSubcutaneous injectionSubcutaneous injection (abdomen, with site rotation)
Key side effectsNosebleeds (epistaxis — most common reported AE), Telangiectasia (visible small blood vessel dilation), Gum bleeding, Elevated hemoglobinInjection site reactions (erythema, pruritus), Peripheral edema, Arthralgia (joint pain), Myalgia
Cited sources2 references5 references

Key differences

  • Evidence level differs: ACE-031 is investigational (in trials), while Tesamorelin is fda-approved.
  • Administration: ACE-031 — Subcutaneous injection; Tesamorelin — Subcutaneous injection (abdomen, with site rotation).
  • Dosing units differ: ACE-031 is dosed in mg/kg, Tesamorelin in mg — they operate at different scales.
  • Frequency: ACE-031 is typically every 2–4 weeks (subcutaneous injection); Tesamorelin is once daily (subcutaneous).
  • Research depth: this profile cites 2 sources for ACE-031 vs 5 for Tesamorelin.

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.

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 ACE-031 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.