Viewing Study NCT03207750


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Study NCT ID: NCT03207750
Status: COMPLETED
Last Update Posted: 2020-12-29
First Post: 2017-06-16
Is NOT Gene Therapy: True
Has Adverse Events: True

Brief Title: This Study Will Evaluate the Immunogenicity, Reactogenicity and Safety of the Routine Infant Vaccines Pediarix®, Hiberix® and Prevenar 13® When Co-administered With GlaxoSmithKline (GSK) Biologicals' Liquid Human Rotavirus Vaccine (HRV) as Compared to GSK's Licensed Lyophilized Vaccine
Sponsor: GlaxoSmithKline
Organization:

Key Dates - Follows AllAPIJSON File Order

Start Date: 2017-09-14
Start Date Type: ACTUAL
Primary Completion Date: 2018-10-09
Primary Completion Date Type: ACTUAL
Completion Date: 2019-03-01
Completion Date Type: ACTUAL
First Submit Date: 2017-06-16
First Submit QC Date: None
Study First Post Date: 2017-07-05
Study First Post Date Type: ACTUAL
Results First Submit Date: 2019-10-08
Results First Submit QC Date: None
Results First Post Date: 2019-10-31
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: 2020-12-07
Last Update Post Date: 2020-12-29
Last Update Post Date Type: ACTUAL