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

PHASE3CompletedINTERVENTIONAL
Enrollment

98

Participants

Timeline

Start Date

February 21, 2011

Primary Completion Date

December 14, 2016

Study Completion Date

September 13, 2017

Conditions
Epilepsy
Interventions
DRUG

Retigabine IR

Flexible dose between 300 mg/day (minimum) and 1200 mg/day (maximum)

Trial Locations (31)

1113

GSK Investigational Site, Sofia

1431

GSK Investigational Site, Sofia

4000

GSK Investigational Site, Plovdiv

9000

GSK Investigational Site, Ghent

10400

GSK Investigational Site, Bangkok

16153

GSK Investigational Site, Genoa

33617

GSK Investigational Site, Bielefeld

40002

GSK Investigational Site, Khon Kaen

40139

GSK Investigational Site, Bologna

49005

GSK Investigational Site, Dnipro

56126

GSK Investigational Site, Pisa

60126

GSK Investigational Site, Torrette Di Ancona

65014

GSK Investigational Site, Odesa

67098

GSK Investigational Site, Strasbourg

67513

GSK Investigational Site, Oleksandrivka Village, Odesa

71100

GSK Investigational Site, Foggia

87042

GSK Investigational Site, Limoges

91045

GSK Investigational Site, Luhansk

107150

GSK Investigational Site, Moscow

117049

GSK Investigational Site, Moscow

193019

GSK Investigational Site, Saint Petersburg

308007

GSK Investigational Site, Belgorod

350007

GSK Investigational Site, Krasnodar

420064

GSK Investigational Site, Kazan'

443095

GSK Investigational Site, Samara

00163

GSK Investigational Site, Rome

00185

GSK Investigational Site, Rome

2103 SW

GSK Investigational Site, Heemstede

00-453

GSK Investigational Site, Warsaw

214 019

GSK Investigational Site, Smolensk

Unknown

GSK Investigational Site, Poltava

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GlaxoSmithKline

INDUSTRY