drugset / Trial / NCT01628393

Efficacy and Safety Study of Ozanimod (RPC1063) in Relapsing Multiple Sclerosis Patients

NCT01628393

Phase 2/3 Completed 258 enrolled Celgene Corporation
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study is a two-part trial consisting of Part A (presented in this record) and Part B (see NCT02047734). The primary objective in Part A of this study was to demonstrate the superior efficacy of ozanimod compared to placebo by showing a reduction in the cumulative number of total gadolinium-enhancing (GdE) lesions from Week 12 to Week 24 in patients with relapsing multiple sclerosis (RMS).

Timeline

Start
2012-09-18
Primary completion
2014-04-13
Completion
2016-05-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Ozanimod Small molecule 0.5 mg Oral
Subject Ozanimod Small molecule 1 mg Oral

Indications