Status:

COMPLETED

The Study Will Evaluate the Efficacy of AZD5423 in Patients With Mild Asthma Challenged With an Inhaled Allergen

Lead Sponsor:

AstraZeneca

Conditions:

Asthma

Eligibility:

All Genders

18-60 years

Phase:

PHASE2

Brief Summary

The purpose of this study is to evaluate the efficacy of AZD5423 in patients with mild asthma challenged with an inhaled allergen.

Eligibility Criteria

Inclusion

  • 18-60 years of age
  • Pre-bronchodilatory FEV1 ≥70% of predicted normal allergic asthmatic with a history of episodic wheeze
  • Positive allergen induced early and late airway bronchoconstriction showing ≥ 20% fall in FEV1 for the early and ≥ 15% for the late response
  • Positive skin prick test to common aeroallergens

Exclusion

  • Any clinically significant disease or disorder
  • Any clinically relevant abnormal finding at screening examinations
  • Smoker or ex-smoker who has stopped smoking \< 12 months prior to study start
  • Worsening of asthma or respiratory infection within 6 weeks from visit 1
  • Allergen-specific immunotherapy within 6 months prior to visit 1

Key Trial Info

Start Date :

November 1 2010

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 1 2011

Estimated Enrollment :

27 Patients enrolled

Trial Details

Trial ID

NCT01225549

Start Date

November 1 2010

End Date

December 1 2011

Last Update

April 2 2015

Active Locations (4)

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Page 1 of 1 (4 locations)

1

Research Site

Calgary, Alberta, Canada

2

Research Site

Hamilton, Ontario, Canada

3

Research Site

Québec, Quebec, Canada

4

Research Site

Saskatoon, Saskatchewan, Canada

The Study Will Evaluate the Efficacy of AZD5423 in Patients With Mild Asthma Challenged With an Inhaled Allergen | DecenTrialz