Skip to main content
SYS · ONLINEPASS · 63.0%
Open Assay
Independent Testing / Est. 2026
BATCH04·26·B
PASS63.0%
N27
PeptidesGH-stackMyostatin Inhibitor (research class)

Myostatin Inhibitor (research class)

/ Heterogeneous class — soluble receptor decoys (ACE-031), monoclonal antibodies (domagrozumab, taldefgrobep), engineered peptide ligands. Vendor product chemistry is typically unspecified.
TIER 3 · PreclinicalN = 0 · TESTING PENDING

ALIAS · Myostatin antagonist (generic) · GDF-8 inhibitor (research)

Pass rate
0
Samples
0
Suppliers
Research use onlyAny dose figures below describe what specific cited studies used, reported factually. Nothing on this page is guidance for human use.READ FIRST →

Terms in this page you can click for a plain-English popup: , , , , , , , .

§ A · Identity
Primary sequence— sequence not captured —
MW · CLASS · Heterogeneous class — soluble receptor decoys (ACE-031), monoclonal antibodies (domagrozumab, taldefgrobep), engineered peptide ligands. Vendor product chemistry is typically unspecified.CATEGORY · GH-stack

Tier 3 by class. 'Myostatin inhibitor' as sold by research-chemical vendors is not a single defined molecule. The pharmacological class includes the failed ACE-031 program, the discontinued domagrozumab antibody (Pfizer DMD trial halted 2018), taldefgrobep alfa (Phase 3 in DMD), and garetosmab (anti-activin A). None are sold as the vendor-labelled 'research myostatin inhibitor peptide'.

§ B · Mechanism of action

Class mechanism: bind myostatin (GDF-8) and prevent its engagement with cell-surface ActRIIB on skeletal muscle, releasing the brake on muscle hypertrophy. The clinical translation has been substantially harder than the rodent data predicted — multiple Phase 2/3 programs have failed primary endpoints in muscular dystrophies, sarcopenia, and recovery indications.

§ C · Human clinical evidence

Class evidence is mixed-to-negative in late-stage human trials. ACE-031 halted for safety; domagrozumab Phase 2 in DMD missed primary endpoint and was terminated; bimagrumab Phase 2 in sporadic IBM showed muscle volume gains without functional benefit; taldefgrobep Phase 3 in DMD ongoing as of 2025. Rodent muscle-mass effects do not translate cleanly to human function.

§ F · Safety signal

Class concerns: ActRIIB-decoy molecules carry vascular off-target risk (ACE-031 epistaxis/telangiectasia signal); monoclonal antibodies have variable injection-site / immunogenicity profiles. Vendor research peptides have no human safety data.

§ H · Regulatory status

Regulatory status

FDA status:
Not FDA-approved
§ I · Notable gaps and controversies

The vendor-sold 'myostatin inhibitor research peptide' has no defined sequence in published literature, no PK data, and no biological characterisation independent of the seller's marketing claims. Cannot be assumed pharmacologically equivalent to any of the named clinical-stage molecules.