Literature DB >> 27659218

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

Rosa Antonijoan1,2, Jimena Coimbra1, Consuelo García-Gea1, Montserrat Puntes1, Ignasi Gich1,2, Cristina Campo3, Román Valiente3, Luis Labeaga3.   

Abstract

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 μg 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 (cm2) were quantified using the Visitrak System. Itching sensation was evaluated using a 100 mm 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&amp;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.

Entities:  

Keywords:  Antihistamine; bilastine; desloratadine; histamine cutaneous challenge; rupatadine

Mesh:

Substances:

Year:  2016        PMID: 27659218     DOI: 10.1080/03007995.2016.1240665

Source DB:  PubMed          Journal:  Curr Med Res Opin        ISSN: 0300-7995            Impact factor:   2.580


  4 in total

Review 1.  Bilastine 10 and 20 mg in paediatric and adult patients: an updated practical approach to treatment decisions.

Authors:  Amalia Leceta; Aintzane García; Ander Sologuren; Cristina Campo
Journal:  Drugs Context       Date:  2021-08-10

Review 2.  Bilastine in allergic rhinoconjunctivitis and urticaria: a practical approach to treatment decisions based on queries received by the medical information department.

Authors:  Amalia Leceta; Ander Sologuren; Román Valiente; Cristina Campo; Luis Labeaga
Journal:  Drugs Context       Date:  2017-02-03

3.  Suppression of wheal and flare in histamine test by the main H1 antihistamines commercialized in Brazil.

Authors:  Helena Maciel-Guerra; Mariana Álvares Penha; Marília Formentini Scotton Jorge; Ricardo da Silva Libório; Ana Cláudia Nazareno Dos Anjos Carrijo; Maria Rita Parise-Fortes; Hélio Amante Miot
Journal:  An Bras Dermatol       Date:  2018-03       Impact factor: 1.896

Review 4.  The safety and tolerability profile of bilastine for chronic urticaria in children.

Authors:  Nikolaos G Papadopoulos; Torsten Zuberbier
Journal:  Clin Transl Allergy       Date:  2019-10-23       Impact factor: 5.871

  4 in total

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