Effects of ICA-105665 Using the Intradermal Capsaicin and Ultraviolet B (UV-B) Models in Healthy Male Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

25

Participants

Timeline

Start Date

August 31, 2009

Primary Completion Date

December 31, 2009

Study Completion Date

December 31, 2009

Conditions
Healthy
Interventions
DRUG

ICA-105665

Subjects randomized to receive ICA -105665 will receive 200 mg BID

DRUG

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.

DRUG

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."

Trial Locations (2)

M23 9QZ

Pfizer Investigational Site, Wythenshawe

Unknown

Pfizer Investigational Site

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY