drugset / Trial / NCT01423110
Efficacy, Safety and Tolerability of BYM338 in Patients With Sporadic Inclusion Body Myositis
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Bimagrumab | Monoclonal antibody | — | — |