study comparing budesonide hydrofluoroalkane (HFA) vs chlorofluorocarbon (CFC) pressurized metered dose inhalers (pMDI) in patients with mild to moderate asthma

Study identifier:D5252C00008

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

A Phase 3, randomised, open-label, crossover study to compare HFA vs CFC pMDI formulations of budesonide on methacholine hyper-reactivity in patients with stable, persistent, mild to moderate asthma

Medical condition

asthma

Phase

Phase 3

Healthy volunteers

No

Study drug

Budesonide HFA, Budesonide CFC

Sex

All

Actual Enrollment

99

Study type

Interventional

Age

18 Years - 65 Years

Date

Study Start Date: 01 Apr 2008
Primary Completion Date: 01 May 2009
Study Completion Date: 01 May 2009

Study design

Allocation: Randomized
Endpoint Classification: Bio-equivalence Study
Intervention Model: Crossover Assignment
Masking: Open Label
Primary Purpose: Treatment

Verification:

Verified 01 Oct 2012 by AstraZeneca Pharmaceuticals

Sponsors

AstraZeneca Pharmaceuticals

Collaborators

-

Inclusion and exclusion criteria