311
Participants
Start Date
January 31, 2012
Primary Completion Date
July 31, 2013
Study Completion Date
July 31, 2013
GW685698/GW642444 (fluticasone furoate/vilanterol trifenatate)
ICS/LABA combination (100/25mcg) administered once daily in the evening via a Novel Dry Powder Inhaler (NDPI)
Placebo
Placebo administered once daily in the evening via a NDPI
GSK Investigational Site, Quezon City
GSK Investigational Site, Marilao, Bulacan
GSK Investigational Site, Beijing
GSK Investigational Site, Beijing
GSK Investigational Site, Beijing
GSK Investigational Site, Shenyang
GSK Investigational Site, Shanghai
GSK Investigational Site, Qingdao
GSK Investigational Site, Hangzhou
GSK Investigational Site, Hangzhou
GSK Investigational Site, Chongqing
GSK Investigational Site, Ilsanseo-gu, Goyang-si, Gyeonggi-do
GSK Investigational Site, Shenzhen
GSK Investigational Site, Zhanjiang
GSK Investigational Site, Nanning
GSK Investigational Site, Haikou
GSK Investigational Site, Xi'an
GSK Investigational Site, Yinchuan
GSK Investigational Site, Chongqing
GSK Investigational Site, Bucheon-si, Gyeonggi-Do
GSK Investigational Site, Cheongju, Chungcheongbuk-do
GSK Investigational Site, Pusan
GSK Investigational Site, Seongnam-si, Gyeonggi-do
GSK Investigational Site, Seoul
GSK Investigational Site, Seoul
GSK Investigational Site, Seoul
GSK Investigational Site, Seoul
GSK Investigational Site, Seoul
Lead Sponsor
GlaxoSmithKline
INDUSTRY