A pharmacokinetic comparison of orally inhaled budesonidedelivered via SkyePharma HFA metered dose inhaler and marketed CFC metered dose inhaler (Pulmicort , AstraZeneca) in healthy male and female volunteers.

Study identifier:D5252C00001

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

A pharmacokinetic comparison of orally inhaled budesonidedelivered via SkyePharma HFA metered dose inhaler and marketed CFC metered dose inhaler (Pulmicort , AstraZeneca) in healthy male and female volunteers.

Medical condition

asthma

Phase

Phase 1

Healthy volunteers

Study drug

Sex

Actual Enrollment

Study type

Interventional

Age

Date

Study Start Date: 01 Jun 2002

Primary Completion Date: -

Study Completion Date: -

Study design

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

Verification:

Verified 01 Nov 2013 by AstraZeneca

Collaborators

Inclusion and exclusion criteria

No locations available

Arms	Assigned Interventions

Documents available

https://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_MED_6111&studyid=2073&filename=CSR-D5252C00001.pdf
Download
CSR-D5252C00001.pdf
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Trial Results Summaries
Available here

A pharmacokinetic comparison of orally inhaled budesonidedelivered via SkyePharma HFA metered dose inhaler and marketed CFC metered dose inhaler (Pulmicort , AstraZeneca) in healthy male and female volunteers.

Official Title

Medical condition

Phase

Healthy volunteers

Study drug

Sex

Actual Enrollment

Study type

Age

Date

Study design

Verification:

Sponsors

Collaborators

Inclusion Criteria

Exclusion Criteria

Documents available

https://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_MED_6111&studyid=2073&filename=CSR-D5252C00001.pdf

CSR-D5252C00001.pdf

Trial Results Summaries