Overview

Ciclesonide for the Treatment of Airway Hyperresponsiveness

Status:
Completed
Trial end date:
2011-10-01
Target enrollment:
Participant gender:
Summary
The study objective is to investigate in a placebo-controlled, double-blind manner the effect of inhaled corticosteroid (ciclesonide) on airway hyperresponsiveness measured as having PD15 mannitol. Treatment medication will be administered as follows: 320 microgram ciclesonide or placebo will be inhaled once daily. The study duration consists of a treatment period of 4 weeks. The study will provide further data on safety of ciclesonide.
Phase:
Phase 4
Details
Lead Sponsor:
AstraZeneca
Treatments:
Ciclesonide