ACE-031
ACE-031
Also known as: ActRIIB-Fc, ACE031, ACVR2B-Fc
Overview
Key Facts
Primary Goal: A soluble form of the activin type IIB receptor fused to a human IgG1 Fc domain
A soluble form of the activin type IIB receptor fused to a human IgG1 Fc domain. It functions as a decoy receptor, binding myostatin, activin, GDF-11, and other TGF-beta superfamily ligands before they can signal through their natural receptors. Originally developed for Duchenne muscular dystrophy, trials were halted due to off-target vascular effects. Half-Life 10-15 days (Fc fusion extends half-life) Typical Dose 0.5–3 mg Frequency Once every 2 weeks (based on clinical trial dosing) Cycle Length 8-12 weeks (limited to research context)
Dosing Information
Half-Life
10-15 days (Fc fusion extends half-life)
Typical Dose
0.5–3 mg
Frequency
Once every 2 weeks (based on clinical trial dosing)
Cycle Length
8-12 weeks (limited to research context)
Administration Routes:
Storage & Reconstitution
Unreconstituted (Powder)
Reconstituted (Mixed)
Research Summary
A Phase II trial in boys with Duchenne muscular dystrophy (NCT01099761) showed dose-dependent increases in lean body mass and bone mineral density. However, the trial was discontinued due to epistaxis and telangiectasias attributed to off-target inhibition of BMP-9/10. Subsequent research by Acceleron led to more selective agents (luspatercept) that avoid the vascular side effects. ACE-031 remains a proof of concept for the ActRIIB pathway in muscle growth.
Frequently Asked Questions
Common questions about ACE-031
UK-Specific Information
Exclusive data points and guidance for UK residents using ACE-031
UK Lab Testing
US Lab Testing
Recommended labs: Quest Diagnostics, LabCorp ($120-$200 for peptide safety panel)
Why this matters: UK-specific lab testing guidance not available on US competitor sites
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Note: Peptide stacking should only be done under the guidance of a qualified healthcare professional. Individual responses may vary.