The purpose of this exploratory trial is to assess the anti-inflammatory effect(s) of topical R115866 in a model of UVB-induced inflammation and in a model of cutaneous irritation.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
SINGLE
Enrollment
12
Topical Application (20 mg)
Topical Application (20 mg)
Department of DermatopathologyCentre Hospitalier Universitaire du Sart Tilman
Liège, Belgium
Primary efficacy endpoint was the mean value of TEWL (Trans-epidermal water loss)
Time frame: Day 1 through Day 9 of treatment
Erythema
Time frame: Day 1 through Day 8 of treatment and Day 15 post-treatment
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.