Viewing Study NCT02394561


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Study NCT ID: NCT02394561
Status: COMPLETED
Last Update Posted: 2019-04-23
First Post: 2015-02-25
Is NOT Gene Therapy: True
Has Adverse Events: True

Brief Title: A 24-week, Multicenter, proSpective stUdy to Evaluate the PASI 90 Clinical Response Rate and the Safety PRofile of sEcukinuMab 300 mg in Cw6-negativE and Cw6-positive Patients With Moderate to Severe Chronic Plaque-type Psoriasis (SUPREME)
Sponsor: Novartis Pharmaceuticals
Organization:

Key Dates - Follows AllAPIJSON File Order

Start Date: 2015-04-10
Start Date Type: ACTUAL
Primary Completion Date: 2017-06-08
Primary Completion Date Type: ACTUAL
Completion Date: 2017-06-08
Completion Date Type: ACTUAL
First Submit Date: 2015-02-25
First Submit QC Date: None
Study First Post Date: 2015-03-20
Study First Post Date Type: ESTIMATED
Results First Submit Date: 2018-06-07
Results First Submit QC Date: None
Results First Post Date: 2019-04-23
Results First Post Date Type: ACTUAL
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: 2019-04-21
Last Update Post Date: 2019-04-23
Last Update Post Date Type: ACTUAL