Viewing Study NCT01323634


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Study NCT ID: NCT01323634
Status: COMPLETED
Last Update Posted: 2017-11-08
First Post: 2011-03-17
Is NOT Gene Therapy: True
Has Adverse Events: True

Brief Title: Study to Evaluate the 24-Hour Pulmonary Function Profile of Fluticasone Furoate (FF) /GW642444 (Vilanterol) (VI) Inhalation Powder 100/25mcg Once Daily Compared With Fluticasone Propionate/Salmeterol Inhalation Powder 250/50mcg Twice Daily in Subjects With Chronic Obstructive Pulmonary Disease
Sponsor: GlaxoSmithKline
Organization:

Key Dates - Follows AllAPIJSON File Order

Start Date: 2011-03-18
Start Date Type: ACTUAL
Primary Completion Date: 2011-12-14
Primary Completion Date Type: ACTUAL
Completion Date: 2011-12-14
Completion Date Type: ACTUAL
First Submit Date: 2011-03-17
First Submit QC Date: None
Study First Post Date: 2011-03-25
Study First Post Date Type: ESTIMATED
Results First Submit Date: 2013-05-30
Results First Submit QC Date: None
Results First Post Date: 2013-07-30
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: 2012-06-18
Disp First Post Date Type: ESTIMATED
Last Update Submit Date: 2017-10-09
Last Update Post Date: 2017-11-08
Last Update Post Date Type: ACTUAL