The purpose of this study is to assess the safety, tolerability and efficacy of KP-413 topical ointment compared with vehicle ointment in treating adult subjects with atopic dermatitis (AD).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
58
Study drug ointment to be applied topically to the selected treatment areas on the head/neck and torso/limbs twice a day for 4 weeks.
Michigan Center for Research Corp
Clinton Twp., Michigan, United States
Oregon Medical Research Center, PC
Portland, Oregon, United States
DermResearch, Inc.
Austin, Texas, United States
J & S Studies, Inc.
College Station, Texas, United States
Investigator's Global Severity Score(IGSS)
Time frame: 4 weeks
Plasma levels of KP-413
Time frame: 6 weeks
Signs and Symptoms of AD
Time frame: 4 weeks
Subject's Numerical Rating Scale(NRS) of Pruritus Score
Time frame: 4 weeks
Percent of AD-affected body surface area (BSA)
Time frame: 4 weeks
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Dermatology Treatment & Research Center, PA
Dallas, Texas, United States
The Education & Research Foundation, Inc
Lynchburg, Virginia, United States