drugset / Trial / NCT01742052

Dose-finding Study of MT-1303

NCT01742052

Phase 2 Completed 415 enrolled Tanabe Pharma Corporation
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objectives of the study are: * To evaluate the effects of three oral doses of MT-1303 compared to placebo given for a period of 24 weeks in subjects with relapsing-remitting multiple sclerosis (RRMS) on MRI parameters * To evaluate the safety and tolerability of three oral doses of MT-1303 compared to placebo given for a period of 24 weeks in subjects with RRMS.

Timeline

Start
2013-01
Primary completion
2014-07
Completion
2014-10

Drugs

EvaluationDrugModalityDoseRoute
Subject amiselimod Small molecule Oral