Drugs / Trevogrumab
last change May 2026 re-read 2 minutes ago

Trevogrumab

Monoclonal antibody targets MSTN via inhibition

Developed for
inclusion body myositis · muscular atrophy · obesity disorder
Investigated by
Regeneron Pharmaceuticals · Sanofi

Trials 8 · a red edge is where a trial was stopped

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 15 trials
Phase 1 NCT02943239 Dec 2016 → Apr 2019 Regeneron Pharmaceuticals Completed No outcome recorded
Phase 1 NCT02741739 Mar → Apr 2016 Regeneron Pharmaceuticals Completed No outcome recorded
Phase 1 NCT01910220 Aug 2013 → Jun 2014 Regeneron Pharmaceuticals Completed No outcome recorded
Phase 1 NCT01720576 Oct 2012 → Jun 2013 Regeneron Pharmaceuticals Completed No outcome recorded
Phase 1 NCT01507402 Jan → Nov 2012 Regeneron Pharmaceuticals Completed No outcome recorded
Phase 23 trials
Phase 2 NCT06299098 Mar 2024 → May 2026 overdue obesity disorder Regeneron Pharmaceuticals Active not recruiting No outcome recorded
Phase 2 NCT03710941 Feb 2019 → Aug 2020 inclusion body myositis Regeneron Pharmaceuticals Withdrawn No outcome recorded
Phase 2 NCT01963598 Nov 2013 → Jan 2015 muscular atrophy Regeneron Pharmaceuticals Completed No outcome recorded

Evidence & citations 9 cited values

Every value below carries the sentence it was read from. 9 sources stand behind the page.

FieldValueCited text
Known as Trevogrumab ClinicalTrials.gov intervention name — accepted as the source's own label NCT06299098
Known as Human igg4 anti-myostatin mab ChEMBL registry synonym — accepted as the source's own label CHEMBL3545374
Known as REGN1033 ClinicalTrials.gov intervention name — accepted as the source's own label NCT01963598
6

NCT01720576

NCT03710941

NCT02741739

NCT01507402

NCT01910220

NCT02943239

Known as SAR391786 “This is a randomized, double-blind, placebo-controlled, single ascending dose study to assess the safety and tolerability of Intravenous (IV) and Subcutaneous (SC)...” NCT01507402
3

“This is a randomized, double-blind, placebo-controlled, multicenter phase 2 study of the safety and efficacy of 3-month subcutaneous (SC) REGN1033 (SAR391786) treatment in...” NCT01963598

“subcutaneously administered REGN1033 (SAR391786) in healthy volunteers.” NCT01720576

“Study to Assess the Safety and Bioeffect of REGN1033 (SAR391786)” NCT01910220

Action Inhibit “Growth/differentiation factor 8 inhibitor” CHEMBL3545374
Modality Monoclonal antibody CHEMBL3545374
Route Intravenous Intravenous (IV) and Subcutaneous (SC) REGN1033(SAR391786)” NCT01507402
Route Subcutaneous “Intravenous (IV) and Subcutaneous (SC) REGN1033(SAR391786)” NCT01507402
Target MSTN “Growth/differentiation factor 8 inhibitor” CHEMBL3545374