25
Participants
Start Date
August 31, 2009
Primary Completion Date
December 31, 2009
Study Completion Date
December 31, 2009
ICA-105665
Subjects randomized to receive ICA -105665 will receive 200 mg BID
Ibuprofen
Subjects randomized to receive Ibuprofen will receive placebo to ICA-105665 at all scheduled dosing times on Days 1 to 4 and a single dose of 800 mg Ibuprofen on the morning of Day 4.
Placebo
"Subjects randomized to receive placebo will receive placebo to ICA~-105665 at all scheduled dosing times on Days 1 to 4 and placebo to Ibuprofen on the morning of Day 4."
Pfizer Investigational Site, Wythenshawe
Pfizer Investigational Site
Lead Sponsor
Pfizer
INDUSTRY