32
Participants
Start Date
May 31, 2011
Primary Completion Date
September 30, 2011
Study Completion Date
September 30, 2011
PF-05105679
Subjects will receive single ascending doses of PF-05105679 or placebo to investigate safety/tolerability and pharmacokinetics of PF-05105679
PF-05105679
Subjects will receive single ascending doses of PF-05105679 or placebo to investigate safety/tolerability and pharmacokinetics of PF-05105679
PF-05105679
Subject will be randomized to a treatment sequence, and assigned to placebo, 2 separate single doses of PF-05105679 in the fasted state and to controlled-release Oxycodone 20 mg (positive control) , with at least one week wash-out between doses.
Pfizer Investigational Site, Brussels
Lead Sponsor
Pfizer
INDUSTRY