Premium
Effect of Desonide Hydrogel 0.05% on the Hypothalamic‐Pituitary‐Adrenal Axis in Pediatric Subjects with Moderate to Severe Atopic Dermatitis
Author(s) -
Eichenfield Lawrence F.,
Basu Sarmistha,
Calvarese Barry,
Trancik Ronald J.
Publication year - 2007
Publication title -
pediatric dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.542
H-Index - 73
eISSN - 1525-1470
pISSN - 0736-8046
DOI - 10.1111/j.1525-1470.2007.00405.x
Subject(s) - medicine , tolerability , atopic dermatitis , adverse effect , cosyntropin , corticosteroid , hypothalamic–pituitary–adrenal axis , dermatology , adrenocorticotropic hormone , hormone
Desonide, a low potency corticosteroid, has been used widely as a topical treatment for inflammatory dermatoses for over 30 years. A recent formulation advance has enabled the development of desonide 0.05% into a novel moisturizing aqueous gel (hydrogel) that is free of alcohol and surfactants. This multicenter, open‐label study evaluated the hypothalamic‐pituitary‐adrenal axis suppression potential, tolerability, and efficacy of this new Class VI topical steroid formulation in pediatric subjects with moderate‐to‐severe atopic dermatitis (mean body surface area = 51%). Forty children, aged 6 months to 6 years were enrolled and treated twice daily for 4 weeks. Desonide hydrogel 0.05% was well tolerated and no treatment‐related adverse events were reported. No suppression of adrenal function was observed in subjects who completed the study without protocol violations related to cosyntropin administration or cortisol testing ( n = 34). Of the subjects who completed the study with complications in cortisol testing ( n = 3), there was one subject (1/37 = 3%) who had a low poststimulation cortisol level at week 4. Efficacy was demonstrated by marked improvement in overall disease state and in the signs and symptoms of atopic dermatitis. This study validates the systemic safety of a novel desonide hydrogel formulation in young pediatric patients and confirms the longstanding tolerability and efficacy profile of desonide.