The principle aim of this study is to obtain safety, tolerability and pharmacokinetic data when LEO 39652 cream is administered cutaneously as single dose to subjects with atopic dermatitis and to healthy subjects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Enrollment
23
Covance Clinical Research Unit, Hyde Street, Leeds, UK
Leeds, United Kingdom
Covance Royal Liverpool Clinical Research Unit
Liverpool, United Kingdom
Number of subjects with adverse events and change from baseline in vital signs (blood pressure, pulse rate) ECG, clinical laboratory and local tolerability assessments
Time frame: Up to 48 hours after dosing
LEO 39652 and metabolites in blood
Time frame: Up to 48 hours after dosing
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