A 3-Month, multi-centre, double-blinded, double-dummy, randomised, parellel group, phase III study to investigate the Efficacy and Safety of Formoterol HFA pMDI compared with Placebo and Oxis Turbuhaler in subjects with asthma.

Study identifier:D5125C00344

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

A 3-Month, multi-centre, double-blinded, double-dummy, randomised, parellel group, phase III study to investigate the Efficacy and Safety of Formoterol HFA pMDI compared with Placebo and Oxis Turbuhaler in subjects with asthma.

Medical condition

asthma

Phase

Phase 3

Healthy volunteers

-

Study drug

-

Sex

-

Actual Enrollment

-

Study type

Interventional

Age

-

Date

Study Start Date: 01 May 2002
Primary Completion Date: -
Study Completion Date: -

Study design

Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -

Verification:

Verified 01 Nov 2013 by AstraZeneca

Sponsors

AstraZeneca

Collaborators

-

Inclusion and exclusion criteria