drugset / Trial / NCT01336621

Long-Term Safety Study of Retigabine Immediate Release (IR) as Adjunctive Therapy in the Treatment of Adults With Partial-Onset Seizures (POS)

NCT01336621 ↗

Phase 3 Completed 98 enrolled GlaxoSmithKline
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this Phase III study is to assess the long-term safety, tolerability and efficacy of flexibly dosed retigabine Immediate Release (IR) as adjunctive therapy in adult subjects with partial-onset seizures. In addition, those subjects who successfully completed 20 weeks of adjunctive treatment with retigabine IR in the parent study, RGB113905, and who were thought to have benefitted from treatment will be provided continued access to retigabine IR.

Timeline

Start
2011-02-21
Primary completion
2016-12-14
Completion
2017-09-13

Drugs

EvaluationDrugModalityDoseRoute
Subject Retigabine IR Unknown — —

Indications