Overview
CP-481,715 Nickel Allergy Study.
Status:
Completed
Completed
Trial end date:
2005-10-01
2005-10-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
To evaluate the suitability of contact allergy as a method for the evaluation of c-chemokine receptor-1 antagonist.Phase:
Phase 1Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
PfizerTreatments:
Nickel
Criteria
Inclusion Criteria:- A history of nickel allergy confirmed by a visual positive reaction (graded at least
++) to T.R.U.E. TEST.
Exclusion Criteria:
- Subjects with evidence or history of clinically significant hematological, renal,
endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric,
neurologic, or allergic disease (including drug allergies, but excluding contact
allergic dermatitis or untreated, asymptomatic, seasonal allergies at time of dosing).