Efficacy and safety of on‐demand versus daily rupatadine in chronic spontaneous urticaria: A randomized trial

Author:

Weller Karsten12ORCID,Gimenez‐Arnau Ana Maria3ORCID,Baron Jens4,Brehler Randolf5,Ferrer Marta67ORCID,Groffik Adriane8,Grundmann Sonja9,Jakob Thilo10,Labrador‐Horrillo Moisés11,Müller Sabine12,Staubach Petra13,Wurpts Gerda14,Metz Martin12ORCID,Maurer Marcus12ORCID

Affiliation:

1. Fraunhofer Institute for Translational Medicine and Pharmacology ITMP, Allergology and Immunology Berlin Germany

2. Institute of Allergology, Charité‐Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt‐Universität zu Berlin Berlin Germany

3. Department of Dermatology, Hospital del Mar, IMIM Universitat Pompeu Fabra Barcelona Spain

4. Department of Dermatology and Allergy University Hospital, RWTH Aachen Aachen Germany

5. Department of Dermatology University Hospital Muenster Muenster Germany

6. Department of Allergy Clinica Universidad de Navarra Pamplona Spain

7. RICORS Red De Enfermedades Inflamatorias (REI)‐RD21/0002/0028 Madrid Spain

8. Department of Dermatology University Medical Center Mainz Mainz Germany

9. Hospital of Dermatology Bad Rothenfelde Germany

10. Department of Dermatology and Allergy, University Medical Center Justus Liebig University Gießen Giessen Germany

11. Allergy Department, Hospital Universitario Vall d'Hebron, VHIR Universitat Autònoma de Barcelona Barcelona Spain

12. Department of Dermatology, Medical Center – University of Freiburg, Faculty of Medicine University of Freiburg Freiburg Germany

13. Department of Dermatology and Allergy University Medical Center Mainz Germany

14. Clinic for Dermatology and Allergology, Aachen Comprehensive Allergy Center (ACAC) Uniklinik RWTH Aachen Aachen Germany

Abstract

AbstractBackgroundNon‐sedating H1‐antihistamines (nsAH) are the most commonly used treatment for chronic spontaneous urticaria (CSU). Many patients use them as on‐demand (OD) therapy rather than a maintenance treatment. Here, we compared OD versus daily maintenance treatment with the nsAH rupatadine, assessed the efficacy of rupatadine updosing, and investigated potential long‐term disease‐modifying effects.MethodsThis multicenter, randomized study consisted of 2 weeks of screening, 8 weeks of double‐blind treatment, and 6 weeks of treatment‐free follow‐up (OD allowed). Adult patients were randomized to 10 mg rupatadine OD or 10 mg rupatadine daily. At Week 4, if patients did not have a complete response, they switched from 10 to 20 mg rupatadine daily or underwent sham updosing (patients on 10 mg rupatadine OD). The primary aim was to compare CSU disease activity at the end of follow‐up between daily versus OD. Additionally, we assessed the efficacy of rupatadine updosing. Major outcomes were disease activity, CSU‐related quality of life (QoL), and disease control.ResultsAt Week 4, disease activity and QoL significantly improved in daily versus OD‐treated patients. Updosing of rupatadine did not improve the mean disease activity, but the number of complete responders increased during updosing from 5% to 22%. At the end of follow‐up, the disease activity of patients treated OD versus daily was not significantly different.ConclusionsDaily rupatadine treatment significantly improved CSU disease activity and QoL during treatment versus OD treatment but not after discontinuation of rupatadine, indicating the benefits of a daily maintenance nsAH schedule.

Publisher

Wiley

Subject

Immunology,Immunology and Allergy

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