The primary objective of this trial is to investigate the safety and tolerability of LEO 138559 in healthy subjects and subjects with moderate to severe atopic dermatitis. The secondary objective of this trial is to study the pharmacokinetics and pharmacodynamics following administration of LEO 138559 to healthy subjects and subjects with moderate to severe atopic dermatitis. Healthy subjects will be exposed to 7 different dose regimens of LEO 138559 (one dose regimen per subject). Subjects with moderate to severe atopic dermatitis will be exposed to 2 different dose regimens of LEO 138559 (one dose regimen per subject).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
47
LEO 138559 is a compound in development at LEO Pharma A/S
LEO 138559 placebo
Investigational site
Leeds, United Kingdom
Investigational site
Liverpool, United Kingdom
LEO Pharma investigational site
Manchester, United Kingdom
Safety of LEO 138559 - numbers of subjects with adverse events
Time frame: Day 1 to Day 120
Safety of LEO 138559 - number of adverse events
Time frame: Day 1 to Day 120
Tolerability of LEO 138559 - number of local site reactions
Time frame: Day 1 to Day 120
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