32
Participants
Start Date
October 19, 2006
Primary Completion Date
December 15, 2006
Study Completion Date
December 15, 2006
Relacatib
Subjects will administer 60 or 120 mg tablets in Session 2
Acetaminophen
Acetaminophen will be administered orally
Ibuprofen
Ibuprofen will be administered orally
Atorvastatin
Atorvastatin will be administered orally
GSK Investigational Site, Antwerp
GSK Investigational Site, Liège
Lead Sponsor
GlaxoSmithKline
INDUSTRY