Viewing StudyNCT00169455



Ignite Creation Date: 2024-05-05 @ 11:54 AM
Last Modification Date: 2024-10-26 @ 9:16 AM
Study NCT ID: NCT00169455
Status: COMPLETED
Last Update Posted: 2017-01-16
First Post: 2005-09-09

Brief Title: Assess the Immunogenicity of the Human Rotavirus HRV Vaccine After Reconstitution Without Buffering Agent Evaluate the Immunogenicity Reactogenicity Safety of the Vaccine After Storage for 7 d at 37C Following 2 Doses in Healthy Infants
Sponsor:
Organization: GlaxoSmithKline

Study Design

Study Type: INTERVENTIONAL
Expanded Access Type Individual: None
Expanded Access Type Intermediate: None
Expanded Access Type Treatment: None
Patient Registry: None
Target Duration: None
Design Allocation:
Design Intervention Model:
Design Intervention Model Description:
Design Masking Description:
Bio Spec Retention: None
Bio Spec Description: None
Enrollment Count: 450
Enrollment Type: ACTUAL
Design Primary Purpose:
Design Masking:
Phases:
Name
PHASE3
Observational Models:
Time Perspective List:
Who Masked List: