drugset / Trial / NCT01261325

Brivaracetam Efficacy and Safety Study in Subjects With Partial Onset Seizures

NCT01261325 ↗

Phase 3 Completed 768 enrolled UCB Pharma
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study will evaluate the efficacy and safety of brivaracetam at doses of 100 and 200mg/day compared to placebo as adjunctive treatment in adult focal epilepsy subjects with partial onset seizures not fully controlled despite current treatment with 1 or 2 concomitant antiepileptic drugs.

Timeline

Start
2010-12
Primary completion
2014-05
Completion
2014-05

Outcome

Met primary endpoint

registry Brivaracetam 100 mg/Day; p <0.001; Percent reduction over PBO 22.8 (95% CI 13.3 to 31.2) NCT01261325 ↗

registry Placebo vs Brivaracetam 100 mg/Day; p <0.001; Odds ratio (BRV versus PBO) 2.39 (95% CI 1.6 to 3.6) NCT01261325 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Brivaracetam Small molecule 100 mg Oral
Subject Brivaracetam Small molecule 200 mg Oral

Indications