drugset / Trial / NCT00420212

Efficacy and Safety of Oral BG00012 in Relapsing-Remitting Multiple Sclerosis

NCT00420212 ↗

Phase 3 Completed 1234 enrolled Biogen
RandomizedParallel-groupDouble-blindTreatment

Summary

To determine if treatment with BG00012 can decrease the number of MS relapses during a certain time period. To determine if, over time, BG00012 treatment can decrease the number of certain types of brain lesions commonly seen in MS patients and slow down the time it takes for the disease to get worse. The purpose of this study is also to determine the safety of BG00012 and how well it is tolerated. Another goal is to see what effect BG00012 may have on tests and evaluations used to assess MS.

Timeline

Start
2007-01
Primary completion
2011-02
Completion
2011-02

Outcome

Met primary endpoint

paper significantly lower in the two BG-12 groups than in the placebo group (27% with BG-12 twice daily and 26% with BG-12 thrice daily vs. 46% with placebo, P<0.001 for both comparisons) PMID 22992073 ↗

release “DEFINE Study Achieves Primary and All Secondary Endpoints for Both Study Doses” biogen.com ↗

release “demonstrated a highly statistically significant reduction ( p<0.0001 ) in the proportion of patients with RRMS who relapsed” biogen.com ↗

release “In DEFINE, TECFIDERA, administered twice-daily, significantly reduced the proportion of patients who relapsed by 49 percent” biogen.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject dimethyl fumarate Unknown 240 mg Oral