Efficacy and safety of lebrikizumab in adult and adolescent patients with moderate-to-severe atopic dermatitis inadequately controlled with or ineligible for ciclosporin A: a placebo-controlled, randomized phase IIIb clinical study (ADvantage)

Lebrikizumab 250 mg Q2W combined with TCS significantly improved signs and symptoms of AD at week 16 in adults and adolescents with moderate-to-severe AD and history of inadequate response to CsA or for whom CsA was not medically advisable, and those benefits were maintained and/or further improved by week 52. Safety was consistent with the known lebrikizumab safety profile.

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Publication Details

Journal
British Journal of Dermatology
Published
2025-09-22
DOI
https://doi.org/10.1093/bjd/ljaf285
Citations
5
Primary Topic
Dermatology and Skin Diseases
Type
article
Field-Weighted Citation Impact
10.02
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article

Efficacy and safety of lebrikizumab in adult and adolescent patients with moderate-to-severe atopic dermatitis inadequately controlled with or ineligible for ciclosporin A: a placebo-controlled, randomized phase IIIb clinical study (ADvantage)

Marjolein S. de Bruin-Weller, Athanasios Tsianakas, Hwanhee Hong, Ruth Coll et al.
5 citations
British Journal of Dermatology
Dermatology and Skin Diseases
10.02
article

Efficacy and safety of lebrikizumab in adult and adolescent patients with moderate-to-severe atopic dermatitis inadequately controlled with or ineligible for ciclosporin A: a placebo-controlled, randomized phase IIIb clinical study (ADvantage)

Marjolein S. de Bruin-Weller, Athanasios Tsianakas, Hwanhee Hong, Ruth Coll, Jacek Cezary Szepietowski, A. Khemis, Richard Bruce Warren, Stephan Weidinger, Helena Agell, Èric Massana, Meritxell Falqués, Esther Garcia Gil, Yanislav Mihaylov
article en
5 citations

Abstract

Lebrikizumab 250 mg Q2W combined with TCS significantly improved signs and symptoms of AD at week 16 in adults and adolescents with moderate-to-severe AD and history of inadequate response to CsA or for whom CsA was not medically advisable, and those benefits were maintained and/or further improved by week 52. Safety was consistent with the known lebrikizumab safety profile.

British Journal of DermatologyVol. 193(5)
Wrocław University of Science and Technology (PL), University of British Columbia (CA), Manchester Academic Health Science Centre (GB), University Medical Center Utrecht (NL), Wroclaw Medical University (PL), Zentralklinik Bad Berka (DE), University Hospital Schleswig-Holstein (DE), Almirall (Spain) (ES), NIHR Manchester Biomedical Research Centre (GB), AGH University of Krakow (PL), University of Lübeck (DE)
Openalex Percentile: Top 2%
Dermatology and Skin Diseases
10.02
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