Overview
Ibuprofen 5% Topical Gel CIPT
Status:
Completed
Completed
Trial end date:
2013-02-01
2013-02-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
This study will determine the potential of Ibuprofen 5% Topical Gel and its vehicle gel to cause irritation after repeated topical application to the healthy skin of human subjects under controlled conditions.Phase:
Phase 1Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
PfizerTreatments:
Ibuprofen
Criteria
Inclusion Criteria:Healthy male and/or female subjects (to be confirmed by medical history) 18 years of age or
older, female subjects of childbearing potential and males who are using an acceptable form
of birth control, subjects who are free of any systemic or dermatologic disorder
Exclusion Criteria:
Have skin disease at the application site, not willing to stop use of systemic or topical
analgesics, corticosteroids, or antihistamines, unwilling or unable to stop use of
sunscreens, creams, or similar products on the back during the study