172
Participants
Start Date
February 28, 2011
Primary Completion Date
November 30, 2011
Study Completion Date
November 30, 2012
GSK2118436
Subjects in this study receive 150 mg of GSK2118436 twice daily and continue on treatment until disease progression, death, or unacceptable adverse event.
GSK Investigational Site, Westmead
GSK Investigational Site, Waratah
GSK Investigational Site, Nedlands
GSK Investigational Site, New York
GSK Investigational Site, Berlin
GSK Investigational Site, Marseille
GSK Investigational Site, Pittsburgh
GSK Investigational Site, Kiel
GSK Investigational Site, Padua
GSK Investigational Site, Nashville
GSK Investigational Site, Essen
GSK Investigational Site, Ann Arbor
GSK Investigational Site, Lille
GSK Investigational Site, Houston
GSK Investigational Site, Napoli
GSK Investigational Site, Los Angeles
GSK Investigational Site, Boulogne-Billancourt
GSK Investigational Site, San Francisco
GSK Investigational Site, San Francisco
GSK Investigational Site, Villejuif
GSK Investigational Site, Seattle
GSK Investigational Site, Edmonton
GSK Investigational Site, Toronto
GSK Investigational Site, Montreal
Lead Sponsor
GlaxoSmithKline
INDUSTRY