Roidipedia.Compound reference & reporting
06 AUG 2026
CompoundsPeptide Trevogrumab (REGN1033)
PeptideInjectableMyostatin inhibitorMonoclonal antibodyAnti-GDF-8

Trevogrumab (REGN1033)

Also known as REGN1033 · Trevogrumab

Trevogrumab (REGN1033) is a fully human anti-myostatin monoclonal antibody from Regeneron, evaluated for sarcopenia and later combined with an anti-activin antibody and GLP-1 agonists to preserve lean mass during weight loss. It selectively neutralises myostatin and has been explored as a muscle-sparing adjunct.

01 Overview

Trevogrumab binds myostatin with high selectivity, sparing closely related ligands such as GDF-11. Early work targeted age-related sarcopenia, where myostatin blockade increases muscle mass.

More recent interest centres on combining trevogrumab with the anti-activin A antibody garetosmab and with GLP-1-based weight-loss drugs, aiming to blunt the loss of lean mass that accompanies large reductions in body weight. This positions myostatin inhibition as a potential companion to incretin therapy rather than a standalone muscle drug.

02 Mechanism

A fully human IgG4 monoclonal antibody that selectively binds mature myostatin, preventing ActRIIB activation while largely sparing GDF-11 and activin.

03 Dosing

TierDoseRouteNotes
Trial dosing100–600 mgSubQInvestigational fixed dosing, often monthly; not marketed.

04 Effects

EffectMagnitudeEvidence
Preservation of lean massInvestigated for maintaining muscle mass during GLP-1-driven weight loss, alone and with anti-activin antibody.Under studyClinical
Increased muscle mass in sarcopeniaEarly sarcopenia studies showed increases in muscle volume.ModestClinical

05 Side effects

EffectSeverityFrequencyEvidenceCountermeasures
Injection-site reactionsLocal reactions at subcutaneous sites.MildCommonClinical
ImmunogenicityAnti-drug antibodies can develop against the therapeutic antibody.MildUncommonClinical

07 References

REGN1033 (trevogrumab), a myostatin-neutralising antibody: preclinical and clinical developmentRegeneron / clinical trial reports

08 Discussion0 comments

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