The purpose of this study is to evaluate the continued safety and tolerability of FB-401 in subjects 2 years of age or older with mild to moderate atopic dermatitis. FB-401 will be applied topically for up to 48 additional weeks and subjects will be evaluated for safety.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
36
Topical
Center for Dermatology Clinical Research, Inc.
Fremont, California, United States
Multi-Specialty Research Associates, Inc.
Lake City, Florida, United States
MedaPhase, Inc
Newnan, Georgia, United States
DS Research
Clarksville, Indiana, United States
Number of adverse events
Safety evaluations
Time frame: 52 weeks
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