Ligelizumab improves angioedema, disease severity and quality-of-life in patients with chronic spontaneous urticaria

Disease burden is particularly high in Chronic Spontaneous Urticaria (CSU) patients with angioedema, and patients whose signs and symptoms are inadequately controlled by H-antihistamines need new treatment options. Here we report an exploratory analysis, from the ligelizumab Phase 2b study, investig...

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Detalles Bibliográficos
Autores: Metz, Martin|||0000-0002-4070-9976, Bernstein, Jonathan|||0000-0002-3476-1196, Giménez-Arnau, Ana M|||0000-0001-5434-7753, Hide, Michihiro, Maurer, Marcus|||0000-0002-4121-481X, Sitz, Karl, Soong, Weily, Sussman, Gordon|||0000-0002-2202-2513, Hua, Eva|||0000-0001-5781-170X, Barve, Avantika, Barbier, Nathalie|||0000-0001-8052-7862, Balp, Maria Magdalena|||0000-0002-8612-7680, Severin, Thomas
Tipo de recurso: artículo
Fecha de publicación:2022
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:281795
Acceso en línea:https://ddd.uab.cat/record/281795
https://dx.doi.org/urn:doi:10.1016/j.waojou.2022.100716
Access Level:acceso abierto
Palabra clave:Angioedema
Chronic spontaneous urticaria
Dermatology life quality index
IgE
Ligelizumab
Descripción
Sumario:Disease burden is particularly high in Chronic Spontaneous Urticaria (CSU) patients with angioedema, and patients whose signs and symptoms are inadequately controlled by H-antihistamines need new treatment options. Here we report an exploratory analysis, from the ligelizumab Phase 2b study, investigating angioedema occurrence in patients with CSU and describe the changes in angioedema following treatment with ligelizumab, omalizumab, or placebo. Data from the ligelizumab Phase 2b core (ligelizumab 72 mg, 240 mg, omalizumab 300 mg and placebo) and extension study (ligelizumab 240 mg) were used. Changes in Weekly Angioedema Activity Score (AAS7), the Dermatology Life Quality Index (DLQI), and Weekly Urticaria Activity Score (UAS7) among each time point were analyzed for each treatment arm. From a total of 297 patients analyzed, 165 (55.6%) reported angioedema occurrence at baseline, with mean AAS7 ranging 30.6-42.2 across treatment arms. At Week 12 of the core study 87.5%, 84.6%, 75.0%, and 61.0% of patients were angioedema free for ligelizumab 72 mg, 240 mg, omalizumab 300 mg, and placebo arms, respectively. In CSU patients with angioedema at baseline, the largest change from baseline in AAS7 score was observed with ligelizumab 72 mg (-31.9) at week 16 in the core study. Patients with angioedema had a higher mean DLQI at baseline (14.9-16.1) vs. patients without angioedema (10.6-12.0). In patients with angioedema, low AAS7 was significantly associated with complete response on UAS7 (UAS7 = 0) and complete normalization of DLQI (DLQI 0-1). In the Phase 2b study, ligelizumab effectively reduced angioedema and urticaria symptoms, and improve health related quality of life in patients with moderate-to-severe CSU. ; .