drugset / Trial / NCT01930708

A Study Evaluating the Effectiveness of Tecfidera (Dimethyl Fumarate) on Multiple Sclerosis (MS) Disease Activity and Patient-Reported Outcomes

NCT01930708

Phase 4 Completed 1114 enrolled Biogen
NaSingle-groupOpen-labelTreatment

Summary

The primary objective of the study is to estimate the annualized relapse rate (ARR) in participants with Relapsing Remitting Multiple Sclerosis (RRMS) who are treated with dimethyl fumarate (DMF) over a 12-month period. The secondary objectives of this study in this population are to assess the impact of DMF over a 12-month period on participants -reported health-related quality of life (HRQoL) outcomes, additional clinical effectiveness outcomes, and health economics-related outcomes, and to characterize participants-reported adherence to DMF.

Timeline

Start
2013-10-31
Primary completion
2016-03-31
Completion
2020-01-09

Drugs

EvaluationDrugModalityDoseRoute
Subject dimethyl fumarate Unknown 240 mg Oral