Efficacy and Safety of Different Concentrations of ZK245186 in Atopic Dermatitis (AD)



Status:Completed
Conditions:Psoriasis, Dermatology
Therapuetic Areas:Dermatology / Plastic Surgery
Healthy:No
Age Range:18 - 55
Updated:4/21/2016
Start Date:November 2010
End Date:April 2012

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Double-blind, Randomized, Vehicle-controlled, Multicenter, Multinational, Parallel-group Study of the Efficacy and Safety of ZK245186 Ointment in Concentrations of 0.01, 0.03, and 0.1% Over 4 Weeks in Patients With Atopic Dermatitis (AD)

The purpose of this study is to evaluate the efficacy and safety of three concentrations of
a development drug compared to placebo in the treatment of atopic dermatitis.


Inclusion Criteria:

- Diagnosis of atopic dermatitis according to Hanifin and Rajka criteria

- Body surface area affected by atopic dermatitis at or less than 15% at start of
treatment

Exclusion Criteria:

- Pregnancy and breast-feeding

- Conditions that may pose a threat to the patient or effect the outcome of the study

- Wide-spread atopic dermatitis (AD) requiring systemic treatment

- Immuno-compromized conditions

- At least 2 weeks after local AD treatment and treatment with systemic antibiotics

- At least 1 month after systemic AD treatment
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