Viewing StudyNCT00449501



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Last Modification Date: 2024-10-26 @ 9:31 AM
Study NCT ID: NCT00449501
Status: COMPLETED
Last Update Posted: 2011-01-24
First Post: 2007-03-16

Brief Title: A Two-week Study Assessing the Onset of Effect Questionnaire Administered Pre-dose Versus Post-dose in Adult Subjects
Sponsor: AstraZeneca
Organization: AstraZeneca

Organization Data

Organization: AstraZeneca
Class: INDUSTRY
Study ID: D5896C00025
Study Type: None
Study Domain: None
Study Link: None
Lead Sponsor: AstraZeneca
Lead Sponsor Class: INDUSTRY
Responsible Party: None
Responsible Party Title: None
Responsible Party Type: None
Responsible Party Affiliation: None
Old Name: None
Old Organization: None

Collaborators