28
Participants
Start Date
April 30, 2011
Primary Completion Date
June 30, 2011
Study Completion Date
June 30, 2011
Maraviroc
maraviroc 300 mg BID x 5 days
Fosamprenavir/ritonavir
fosamprenavir/ritonavir 700/100 mg BID x 10 days
Maraviroc + Fosamprenavir/ritonavir
maraviroc 300 mg BID + fosamprenavir/ritonavir 700/100 mg BID x 10 days
Maraviroc
maraviroc 300 mg QD x 5 days
Fosamprenavir/ritonavir
fosamprenavir/ritonavir 1400/100 mg QD x 10 days
Maraviroc + Fosamprenavir/ritonavir
maraviroc 300 mg QD + fosamprenavir/ritonavir 1400/100 mg QD x 10 days
Pfizer Investigational Site, Brussels
Lead Sponsor
Collaborators (1)
Pfizer
INDUSTRY
ViiV Healthcare
INDUSTRY