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Rapid and sustained improvements in Generalized Pustular Psoriasis Physician Global Assessment scores with spesolimab for treatment of generalized pustular psoriasis flares in the randomized, placebo-controlled Effisayil 1 study.
Elewski, Boni E; Lebwohl, Mark G; Anadkat, Milan J; Barker, Jonathan; Ghoreschi, Kamran; Imafuku, Shinichi; Mrowietz, Ulrich; Li, Ling; Quaresma, Manuel; Thoma, Christian; Bachelez, Hervé.
Afiliación
  • Elewski BE; University of Alabama School of Medicine, Birmingham, Alabama. Electronic address: belewski@uabmc.edu.
  • Lebwohl MG; Icahn School of Medicine at Mount Sinai, New York, New York.
  • Anadkat MJ; Division of Dermatology, Washington University School of Medicine, St. Louis, Missouri.
  • Barker J; St John's Institute of Dermatology, Guy's and St Thomas' NHS Foundation Trust, London, United Kingdom.
  • Ghoreschi K; Department of Dermatology, Venereology and Allergology, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin Institute of Health, Berlin, Germany.
  • Imafuku S; Department of Dermatology, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.
  • Mrowietz U; Psoriasis-Center, Department of Dermatology, University Medical Center Schleswig-Holstein, Campus Kiel, Kiel, Germany.
  • Li L; Boehringer Ingelheim Investment Co, Ltd, Shanghai, China.
  • Quaresma M; Boehringer Ingelheim International GmbH, Ingelheim, Germany.
  • Thoma C; Boehringer Ingelheim International GmbH, Biberach, Germany.
  • Bachelez H; Service de Dermatologie, Assistance Publique-Hôpitaux de Paris Hôpital Saint-Louis, Paris, France; INSERM Unité 1163, Imagine Institute of Genetic Diseases, Université Paris Cité, Paris, France.
J Am Acad Dermatol ; 89(1): 36-44, 2023 07.
Article en En | MEDLINE | ID: mdl-36870370
ABSTRACT

BACKGROUND:

Effisayil 1 was a randomized, placebo-controlled study of spesolimab, which is an anti-IL-36 receptor antibody, in patients presenting with a generalized pustular psoriasis flare.

OBJECTIVE:

To assess the effects of spesolimab over the 12-week study.

METHODS:

The primary endpoint of the study was Generalized Pustular Psoriasis Physician Global Assessment (GPPGA) pustulation subscore of 0 at week 1. Patients (N = 53) were randomized (21) to receive a single intravenous dose of 900 mg spesolimab or placebo on day 1. Patients could receive open-label spesolimab for persistent flare symptoms on day 8.

RESULTS:

Most patients receiving spesolimab achieved a GPPGA pustulation subscore of 0 (60.0%) and GPPGA total score of 0 or 1 (60.0%) by week 12. In patients randomized to placebo who received open-label spesolimab on day 8, the proportion with GPPGA pustulation subscore of 0 increased from 5.6% at day 8 to 83.3% at week 2. No factors predictive of spesolimab response were identified in patient demographics or clinical characteristics.

LIMITATIONS:

The effect of initial randomization was not determined conventionally beyond week 1 due to patients receiving open-label spesolimab.

CONCLUSION:

Rapid control of generalized pustular psoriasis flare symptoms with spesolimab was sustained over 12 weeks, further supporting its potential use as a therapeutic option for patients.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Psoriasis Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Humans Idioma: En Revista: J Am Acad Dermatol Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Psoriasis Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Humans Idioma: En Revista: J Am Acad Dermatol Año: 2023 Tipo del documento: Article