drugset / Trial / NCT01801917

Efficacy and Tolerability of BAF312 in Patients With Polymyositis

NCT01801917

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

Summary

This study assessed the efficacy, safety and tolerability of BAF312 administered orally in patients with clinically active polymyositis and also in patients with polymyositis who had shown inadequate response to corticosteroids and or DMARDs (disease modifying antirheumatic drugs).

Timeline

Start
2013-04-24
Primary completion
2016-08-05
Completion
2016-08-05

Drugs

EvaluationDrugModalityDoseRoute
Subject BAF312 Unknown 2 mg Oral
Subject BAF312 Unknown 10 mg Oral

Indications