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A 12-week, Randomised, Double-blind, Placebo-controlled, Three-period, Cross-over Pilot Study Comparing the Effect of Salmeterol/Fluticasone Propionate, Fluticasone Propionate and Placebo on Perpheral Blood Eosinophils and Serum IL-5 in Response to Allergen Challenge in Asthma Subjects When Allergen Challenge is Administered at 1 Hour or 11-12 Hours Post-dose of the Dosing Interval

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Trial Profile

A 12-week, Randomised, Double-blind, Placebo-controlled, Three-period, Cross-over Pilot Study Comparing the Effect of Salmeterol/Fluticasone Propionate, Fluticasone Propionate and Placebo on Perpheral Blood Eosinophils and Serum IL-5 in Response to Allergen Challenge in Asthma Subjects When Allergen Challenge is Administered at 1 Hour or 11-12 Hours Post-dose of the Dosing Interval

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 27 Jun 2023

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At a glance

Most Recent Events

  • 12 Mar 2010 Additional trial location identified as reported by ClinicalTrials.gov.
  • 04 Sep 2009 Actual patient number (23) added as reported by ClinicalTrials.gov.
  • 22 Nov 2008 Status changed from recruiting to completed.

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