drugset / Trial / NCT00134563

Study of Teriflunomide in Reducing the Frequency of Relapses and Accumulation of Disability in Patients With Multiple Sclerosis

NCT00134563 ↗

Phase 3 Completed 1088 enrolled Sanofi
RandomizedParallel-groupTriple-blindTreatment

Summary

The primary objective was to determine the effect of teriflunomide on the frequency of relapses in patients with relapsing multiple sclerosis (MS). Secondary objectives were: * to evaluate the effect of teriflunomide on the accumulation of disability as measured by Expanded Disability Status Scale \[EDSS\], the burden of disease as measured by Magnetic Resonance Imaging \[MRI\] and patient-reported fatigue; * to evaluate the safety and tolerability of teriflunomide.

Timeline

Start
2004-09
Primary completion
2010-07
Completion
2010-07

Outcome

Met primary endpoint

registry Placebo vs Teriflunomide 14 mg; p = 0.0005; Relative risk reduction (%) 31.5 NCT00134563 ↗

registry Placebo vs Teriflunomide 7 mg; p = 0.0002; Relative Risk Reduction (%) 31.2 NCT00134563 ↗

paper Teriflunomide reduced the annualized relapse rate (0.54 for placebo vs. 0.37 for teriflunomide at either 7 or 14 mg) PMID 21991951 ↗

paper with relative risk reductions of 31.2% and 31.5%, respectively (P<0.001 for both comparisons with placebo). PMID 21991951 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Teriflunomide Small molecule 7 mg Oral
Subject Teriflunomide Small molecule 14 mg Oral

Indications