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

Curr Med Res Opin. 2017 Jan;33(1):129-136. doi: 10.1080/03007995.2016.1240665. Epub 2016 Oct 21.

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&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.

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

Publication types

  • Comparative Study
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Benzimidazoles / pharmacology*
  • Cross-Over Studies
  • Cyproheptadine / analogs & derivatives*
  • Cyproheptadine / pharmacology
  • Double-Blind Method
  • Female
  • Healthy Volunteers
  • Histamine / pharmacology
  • Histamine Antagonists / pharmacology*
  • Humans
  • Injections, Intradermal
  • Loratadine / analogs & derivatives*
  • Loratadine / pharmacology
  • Male
  • Piperidines / pharmacology*
  • Skin / drug effects*

Substances

  • Benzimidazoles
  • Histamine Antagonists
  • Piperidines
  • rupatadine
  • Cyproheptadine
  • Loratadine
  • Histamine
  • desloratadine
  • bilastine

Associated data

  • EudraCT/2015-000790-13