A Study to assess the concentration of budesonide in breast milk from asthmatic women

Study identifier:D5254C00763

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

An open single centre study to assess the concentration of budesonide in breast milk from asthmatic women on maintenance treatment w/Pulmicort ® Turbuhaler ® at the dose levels 200/400 µg bid

Medical condition

asthma

Phase

Phase 4

Healthy volunteers

No

Study drug

Pulmicort (budesonide) Turbuhaler

Sex

Female

Actual Enrollment

8

Study type

Interventional

Age

N/A

Date

Study Start Date: 01 Sept 2004
Primary Completion Date: -
Study Completion Date: 01 Oct 2005

Study design

Allocation: Non-randomized
Endpoint Classification: Pharmacokinetics Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment

Verification:

Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals

Sponsors

AstraZeneca Pharmaceuticals

Collaborators

-

Inclusion and exclusion criteria