Efficacy and Safety of Bimagrumab/BYM338 at 52 Weeks on Physical Function, Muscle Strength, Mobility in sIBM Patients

Completed · Phase 2/Phase 3 · Has a placebo group

Conditions studied: Sporadic Inclusion Body Myositis

In brief

This study evaluated the efficacy, safety and tolerability of multiple doses of bimagrumab/BYM338 vs placebo, when administered intravenously (i.v.), on physical function, muscle strength, and mobility in patients with sporadic inclusion body myositis (sIBM).

Key facts

Study ID
NCT01925209
Run by
Novartis Pharmaceuticals
People needed
251
Starts
2013-09-26
Expected to finish
2016-01-06
Last updated by the study team
2017-08-11

Who can join

Age: 36 and older, up to 85. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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