98
Participants
Start Date
February 21, 2011
Primary Completion Date
December 14, 2016
Study Completion Date
September 13, 2017
Retigabine IR
Flexible dose between 300 mg/day (minimum) and 1200 mg/day (maximum)
GSK Investigational Site, Sofia
GSK Investigational Site, Sofia
GSK Investigational Site, Plovdiv
GSK Investigational Site, Ghent
GSK Investigational Site, Bangkok
GSK Investigational Site, Genoa
GSK Investigational Site, Bielefeld
GSK Investigational Site, Khon Kaen
GSK Investigational Site, Bologna
GSK Investigational Site, Dnipro
GSK Investigational Site, Pisa
GSK Investigational Site, Torrette Di Ancona
GSK Investigational Site, Odesa
GSK Investigational Site, Strasbourg
GSK Investigational Site, Oleksandrivka Village, Odesa
GSK Investigational Site, Foggia
GSK Investigational Site, Limoges
GSK Investigational Site, Luhansk
GSK Investigational Site, Moscow
GSK Investigational Site, Moscow
GSK Investigational Site, Saint Petersburg
GSK Investigational Site, Belgorod
GSK Investigational Site, Krasnodar
GSK Investigational Site, Kazan'
GSK Investigational Site, Samara
GSK Investigational Site, Rome
GSK Investigational Site, Rome
GSK Investigational Site, Heemstede
GSK Investigational Site, Warsaw
GSK Investigational Site, Smolensk
GSK Investigational Site, Poltava
Lead Sponsor
GlaxoSmithKline
INDUSTRY