drugset / Trial / NCT01423110

Efficacy, Safety and Tolerability of BYM338 in Patients With Sporadic Inclusion Body Myositis

NCT01423110 ↗

Phase 2 Completed 14 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study will assess the efficacy, safety and tolerability of BYM338 in patients with sporadic Inclusion Body Myositis

Timeline

Start
2011-08
Primary completion
2012-05
Completion
2012-05

Outcome

Met primary endpoint

paper Eight weeks after dosing, the bimagrumab-treated patients increased thigh muscle volume (right leg +6.5% compared with placebo, p = 0.024; PMID 25381300 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Bimagrumab Monoclonal antibody — —