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ACE-031

Myostatin inhibitor

ACE-031 molecular structure

Overview

ACE-031 is an experimental drug designed to increase muscle mass by blocking myostatin — the protein that naturally limits how big your muscles can grow. **How it works:** Your body produces myostatin to prevent muscles from growing too large. ACE-031 acts as a "decoy receptor" that intercepts myostatin before it can reach muscle tissue, essentially removing the brakes on muscle growth. **What the research shows:** • Developed initially for muscular dystrophy patients to combat muscle wasting • Clinical trials showed significant increases in lean muscle mass • Also increased bone mineral density in studies • Development was halted due to safety concerns (minor nosebleeds and gum bleeding) **The science behind it:** ACE-031 is a fusion protein combining part of the activin receptor (ActRIIB) with an antibody fragment. This allows it to circulate in the bloodstream and bind to myostatin and related proteins (like activin A and GDF-11) that suppress muscle growth. **Important to know:** Clinical development was discontinued by Acceleron Pharma in 2013 after Phase 2 trials due to safety signals. The compound remains investigational and is not approved for any use. --- **Sources:** Attie KM, et al. (2013) Neuromuscular Disorders. DOI:10.1016/j.nmd.2013.02.015 | Campbell C, et al. (2017) Muscle & Nerve. DOI:10.1002/mus.25268

Last reviewed: 2026-08-18

Identity & Aliases

Also known as

ACE-031 (development code)ACVR2B-FcActRIIB-Fc fusion proteinsoluble activin receptor type IIB

Status: Clinical Trials

Full composition (formula, molecular weight, sequence) in Quick Facts →

Research Areas

Muscle mass and lean body compositionDuchenne muscular dystrophy (DMD)Myostatin/activin signaling blockadeMuscle-wasting disorders

Available Evidence

Human

In a single ascending-dose study in healthy volunteers, ACE-031 (a soluble activin receptor type IIB-Fc fusion protein that neutralizes myostatin and related ligands) produced dose-dependent increases in lean body mass and decreases in fat mass. A randomized, placebo-controlled trial in ambulatory boys with Duchenne muscular dystrophy showed increased lean mass, but epistaxis (nosebleeds) and telangiectasias led to dose reduction and discontinuation of the program.

Animal

ActRIIB ligand-trap constructs increased skeletal muscle mass in rodent models, supporting the myostatin-blockade concept for muscle wasting; the ACE-031 clinical program itself was discontinued after the Phase 2 safety findings.

In Vitro

ACE-031 binds myostatin, activin A and GDF-11 with high affinity, preventing their signaling through activin type II receptors (in-vitro binding assays).

Uncertain

Functional benefit (strength, ambulation) in DMD was not established, and no drug in this class is approved for muscle wasting; claims about use for bodybuilding/performance are entirely unproven.

Key Studies & Findings

2 studies

Benefits & Effects

1 documented

Muscle Mass: 3.3% lean mass increase, study terminated

clinical

No side effects data available yet.

This peptide may have limited safety data.

Limitations & Open Questions

Clinical development was halted after Phase 2 largely because of bleeding-related adverse events (epistaxis, telangiectasias); there are no long-term data on functional outcomes in DMD or other muscle-wasting conditions, and no approved indication.

Pharmacology

ACE-031 is a recombinant fusion protein of the extracellular domain of human activin receptor type IIB fused to an IgG1 Fc region; it sequesters myostatin, activin A and GDF-11, blocking catabolic TGF-beta-family signaling in muscle. It was administered by subcutaneous injection in trials; beyond trial reports, no clinical pharmacokinetic data are published.

Frequently Asked Questions

Is ACE-031 approved for any use?

No. Its clinical development was discontinued after Phase 2 trials due to nosebleeds and telangiectasias; it has no approved indication.

How does ACE-031 increase muscle mass?

It acts as a soluble 'trap' for myostatin, activin A and GDF-11, preventing these ligands from inhibiting muscle growth through activin type II receptors.

Research Citations

1
Gel Electrophoretic Detection of Black Market ACE-031.

Christian Reichel, Thomas Filip, Günter Gmeiner, Mario Thevis (2025)

2
The relationship between myodural bridges, hyperplasia of the suboccipital musculature, and intracranial pressure.

Li C, Yue C, Liu ZC, Gong J, Wei XS, Yang H, Gilmore C, Yu SB, Hack GD, Sui HJ (2022)

3

Gateways to clinical trials.

Tomillero A, Moral MA (2010)

4
The relationship between myodural bridge, atrophy and hyperplasia of the suboccipital musculature, and cerebrospinal fluid dynamics.

Yang H, Wei XS, Gong J, Du XM, Feng HB, Su C, Gilmore C, Yue C, Yu SB, Li C, Sui HJ (2023)

5
Administration of a soluble activin type IIB receptor promotes skeletal muscle growth independent of fiber type.

Cadena SM, Tomkinson KN, Monnell TE, Spaits MS, Kumar R, Underwood KW, Pearsall RS, Lachey JL (2010)

+ 27 more citations

Related Resources

Quick Facts

Sequence

QDGPIPP

Mechanism

Binds to myostatin and other TGF-β family ligands, preventing their inhibitory effects on muscle growth.

Safety Information

No significant safety concerns identified. Standard precautions apply.

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