Status:

COMPLETED

Study Evaluating the Effect of IMA-026 on Allergen-Induced Late Asthma Response in Mild Asthma

Lead Sponsor:

Wyeth is now a wholly owned subsidiary of Pfizer

Conditions:

Asthma

Eligibility:

All Genders

18-60 years

Phase:

PHASE1

Brief Summary

The purpose of this study is to evaluate the effect of IMA-026, an antibody to IL-13, on airway hyperresponsiveness and airway inflammation in mild asthmatics. IMA-026 will be given as 2 injections un...

Eligibility Criteria

Inclusion

  • Healthy men and women 18 to 60 yrs with mild allergic asthma
  • only asthma med is short-acting bronchodilator used not more than twice weekly
  • FEV1 greater than 70% predicted and a demonstrated baseline late response to allergen induction

Exclusion

  • Upper respiratory infection or asthma exacerbation with 4 weeks of screening
  • Serious infection requiring parenteral antibiotics or hospitalization with 4 weeks of test article administration
  • Positive radiographic findings indicative of respiratory disease other than asthma

Key Trial Info

Start Date :

September 1 2008

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

June 1 2009

Estimated Enrollment :

24 Patients enrolled

Trial Details

Trial ID

NCT00725582

Start Date

September 1 2008

End Date

June 1 2009

Last Update

June 2 2009

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