Comparative efficacy of bilastine, desloratadine and rupatadine in the suppression of wheal and flare response induced by intradermal histamine in healthy volunteers


Por: Antonijoan, R, Coimbra, J, Garcia-Gea, C, Puntes, M, Gich, I, Campo, C, Valiente, R, Labeaga, L

Publicada: 1 ene 2017
Resumen:
Objective: To compare the peripheral antihistaminic activity of bilastine, rupatadine and desloratadine in inhibiting the histamine-induced wheal and flare (W&F) response. Research design and methods: Twenty-four healthy volunteers aged 18-40 years participated in this crossover, randomized, double-blind, placebo-controlled clinical study. Subjects received single doses of bilastine 20 mg, desloratadine 5 mg, rupatadine 10 mg and placebo. W&F responses induced by intradermal injection of histamine 5 g were evaluated before treatment (basal value) and at 0.5, 1, 2, 4, 6, 9, 12 and 24 hours after treatment. Fifteen minutes after histamine injection, W&F surface areas (cm(2)) were quantified using the Visitrak System. Itching sensation was evaluated using a 100mm visual analog scale. EudraCT number: 2015-000790-13. Main outcome measures: The primary outcome measure was the percentage reduction in W&F areas after each active treatment compared with corresponding basal values. Results: Bilastine induced the greatest inhibition in wheal area and was significantly superior to desloratadine and rupatadine from 1 to 12 hours (both p <.001). Rupatadine and desloratadine were better than placebo without differences between them. Maximum wheal inhibition occurred at 6 hours (bilastine 83%, desloratadine 38%, rupatadine 37%). Onset of action was 1 hour for bilastine and 4 hours for desloratadine and rupatadine. Bilastine was significantly superior to desloratadine and rupatadine for flare inhibition from 1-24 hours (both p <.001) with an onset of action at 30 minutes. Bilastine was significantly better than desloratadine (2-12 hours; at least p <.05) and rupatadine (2-9 hours; at least p <.01) for reducing itching sensation. Neither desloratadine nor rupatadine significantly reduced itching compared to placebo. All active treatments were well tolerated. Conclusions: Bilastine 20 mg induced significantly greater inhibition of the W&F response compared with desloratadine 5 mg and rupatadine 10 mg throughout the 24 hour study period, and had the fastest onset of action. Only bilastine significantly reduced itching sensation versus placebo.

Filiaciones:
Antonijoan, R:
 Biomed Res Inst St Pau IIB St Pau, Drug Res Ctr CIM, Barcelona, Spain

 UAB, Pharmacol & Therapeut Dept, Bellaterra, Spain

Coimbra, J:
 Biomed Res Inst St Pau IIB St Pau, Drug Res Ctr CIM, Barcelona, Spain

Garcia-Gea, C:
 Biomed Res Inst St Pau IIB St Pau, Drug Res Ctr CIM, Barcelona, Spain

Puntes, M:
 Biomed Res Inst St Pau IIB St Pau, Drug Res Ctr CIM, Barcelona, Spain

Gich, I:
 Biomed Res Inst St Pau IIB St Pau, Drug Res Ctr CIM, Barcelona, Spain

 UAB, Pharmacol & Therapeut Dept, Bellaterra, Spain

Campo, C:
 Faes Farma SA, Clin Res Dept, Leioa 48940, Bizkaia, Spain

Valiente, R:
 Faes Farma SA, Clin Res Dept, Leioa 48940, Bizkaia, Spain

Labeaga, L:
 Faes Farma SA, Clin Res Dept, Leioa 48940, Bizkaia, Spain
ISSN: 03007995





CURRENT MEDICAL RESEARCH AND OPINION
Editorial
TAYLOR & FRANCIS LTD, 2-4 PARK SQUARE, MILTON PARK, ABINGDON OR14 4RN, OXON, ENGLAND, Reino Unido
Tipo de documento: Article
Volumen: 33 Número: 1
Páginas: 129-136
WOS Id: 000392166300018
ID de PubMed: 27659218

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