Viewing Study NCT01862367


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Study NCT ID: NCT01862367
Status: COMPLETED
Last Update Posted: 2019-07-09
First Post: 2013-05-21
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Use of rFXIII in Treatment of Congenital FXIII Deficiency, a Prospective Multi-centre Observational Study
Sponsor: Novo Nordisk A/S
Organization:

Key Dates - Follows AllAPIJSON File Order

Start Date: 2013-05-17
Start Date Type: ACTUAL
Primary Completion Date: 2019-06-26
Primary Completion Date Type: ACTUAL
Completion Date: 2019-06-26
Completion Date Type: ACTUAL
First Submit Date: 2013-05-21
First Submit QC Date: None
Study First Post Date: 2013-05-24
Study First Post Date Type: ESTIMATED
Results First Submit Date: None
Results First Submit QC Date: None
Results First Post Date: None
Results First Post Date Type: None
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: 2019-07-08
Last Update Post Date: 2019-07-09
Last Update Post Date Type: ACTUAL