A dose-response study of the bronchodilator action of azelastine in asthma

J Allergy Clin Immunol. 1987 Jun;79(6):893-9. doi: 10.1016/0091-6749(87)90238-7.

Abstract

Azelastine is an orally effective inhibitor of mediator activity in allergic reactions and has also been demonstrated to have bronchodilator activity. In this randomized, double-blind, placebo-controlled, multicenter study, 150 patients, aged 12 to 60 years, with moderate to severe asthma, received a single oral dose of 2, 4, 8, 12, or 16 mg of azelastine or placebo. Theophylline was stopped 24 hours and other bronchodilators at least 8 hours before the study day. Patients were evaluated for 8 hours after dose by spirometry and were monitored for adverse effects. All doses of azelastine produced bronchodilation with 4 mg greater than 2 mg greater than placebo; higher doses did not increase magnitude or duration of effect. We conclude that azelastine produces significant bronchodilation of long duration. The optimal dose appears to be 4 mg for adolescent and adult patients with asthma.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Adolescent
  • Adult
  • Asthma / drug therapy*
  • Bronchodilator Agents / therapeutic use*
  • Child
  • Clinical Trials as Topic
  • Dose-Response Relationship, Drug
  • Double-Blind Method
  • Humans
  • Kinetics
  • Lung Volume Measurements
  • Middle Aged
  • Phthalazines / therapeutic use*
  • Pyridazines / therapeutic use*
  • Random Allocation
  • Theophylline / blood

Substances

  • Bronchodilator Agents
  • Phthalazines
  • Pyridazines
  • Theophylline
  • azelastine