15
Participants
Start Date
April 30, 2010
Primary Completion Date
June 30, 2010
Study Completion Date
June 30, 2010
Raltegravir
raltegravir 400mg q12h x 5 days (Reference Treatment)
GSK2248761
GSK2248761 200mg q24h x 5 days (Reference Treatment)
GSK2248761 + Raltegravir
GSK2248761 200mg q24h + raltegravir 400mg q12h x 5 days (Test Treatment)
GSK Investigational Site, Buffalo
Lead Sponsor
ViiV Healthcare
INDUSTRY