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Efficacy and safety of dupilumab with concomitant topical corticosteroids in children 6 to 11 years old with severe atopic dermatitis: A randomized, double-blinded, placebo-controlled phase 3 trial.

Authors :
Paller, Amy S.
Siegfried, Elaine C.
Thaçi, Diamant
Wollenberg, Andreas
Cork, Michael J.
Arkwright, Peter D.
Gooderham, Melinda
Beck, Lisa A.
Boguniewicz, Mark
Sher, Lawrence
Weisman, Jamie
O'Malley, John T.
Patel, Naimish
Hardin, Megan
Graham, Neil M.H.
Ruddy, Marcella
Sun, Xian
Davis, John D.
Kamal, Mohamed A.
Khokhar, Faisal A.
Source :
Journal of the American Academy of Dermatology; Nov2020, Vol. 83 Issue 5, p1282-1293, 12p
Publication Year :
2020

Abstract

<bold>Background: </bold>Children with severe atopic dermatitis (AD) have limited treatment options.<bold>Objective: </bold>We report the efficacy and safety of dupilumab + topical corticosteroids (TCS) in children aged 6-11 years with severe AD inadequately controlled with topical therapies.<bold>Methods: </bold>In this double-blind, 16-week, phase 3 trial (NCT03345914), 367 patients were randomized 1:1:1 to 300 mg dupilumab every 4 weeks (300 mg q4w), a weight-based regimen of dupilumab every 2 weeks (100 mg q2w, baseline weight <30 kg; 200 mg q2w, baseline weight ≥30 kg), or placebo; with concomitant medium-potency TCS.<bold>Results: </bold>Both the q4w and q2w dupilumab + TCS regimens resulted in clinically meaningful and statistically significant improvement in signs, symptoms, and quality of life (QOL) versus placebo + TCS in all prespecified endpoints. For q4w, q2w, and placebo, 32.8%, 29.5%, and 11.4% of patients, respectively, achieved Investigator's Global Assessment scores of 0 or 1; 69.7%, 67.2%, and 26.8% achieved ≥75% improvement in Eczema Area and Severity Index scores; and 50.8%, 58.3%, and 12.3% achieved ≥4-point reduction in worst itch score. Response to therapy was weight-dependent: optimal dupilumab doses for efficacy and safety were 300 mg q4w in children <30 kg and 200 mg q2w in children ≥30 kg. Conjunctivitis and injection-site reactions were more common with dupilumab + TCS than with placebo + TCS.<bold>Limitations: </bold>Short-term 16-week treatment period; severe AD only.<bold>Conclusion: </bold>Dupilumab + TCS is efficacious and well tolerated in children with severe AD, significantly improving signs, symptoms, and QOL. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01909622
Volume :
83
Issue :
5
Database :
Supplemental Index
Journal :
Journal of the American Academy of Dermatology
Publication Type :
Academic Journal
Accession number :
146398258
Full Text :
https://doi.org/10.1016/j.jaad.2020.06.054