Viewing Study NCT01772134


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Study NCT ID: NCT01772134
Status: COMPLETED
Last Update Posted: 2018-01-29
First Post: 2013-01-17
Is NOT Gene Therapy: True
Has Adverse Events: True

Brief Title: Efficacy and Safety of the Addition of Fluticanse Propionate/Salmeterol (250/50mcg) Twice-daily to 2 Doses of Umeclidinium Bromide (62.5 or 125mcg) Once-daily Over 12 Weeks
Sponsor: GlaxoSmithKline
Organization:

Key Dates - Follows AllAPIJSON File Order

Start Date: 2013-01-01
Start Date Type: None
Primary Completion Date: 2013-07-01
Primary Completion Date Type: ACTUAL
Completion Date: 2013-07-22
Completion Date Type: ACTUAL
First Submit Date: 2013-01-17
First Submit QC Date: None
Study First Post Date: 2013-01-21
Study First Post Date Type: ESTIMATED
Results First Submit Date: 2014-03-06
Results First Submit QC Date: None
Results First Post Date: 2014-04-16
Results First Post Date Type: ESTIMATED
Results First Post QC Date: None
Results First Post QC Date Type: None
Disp First Submit Date: None
Disp First Submit QC Date: None
Disp First Post Date: None
Disp First Post Date Type: None
Last Update Submit Date: 2018-01-25
Last Update Post Date: 2018-01-29
Last Update Post Date Type: ACTUAL