At a glance
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Immunogenicity and Safety Study of GSK Biologicals' Herpes Zoster Vaccine GSK1437173A When Co-administered With Pneumovax 23™ in Adults Aged 50 Years and Older
In Brief
A Phase 3 clinical trial evaluating Herpes Zoster vaccine GSK 1437173A and Licensed pneumococcal polysaccharide conjugate vaccine (23-valent, adsorbed), Pneumovax 23™ for Herpes Zoster and Herpes Zoster Vaccine. Completed, enrolled 865 participants across 9 sites in 3 countries.
Detailed Summary
The purpose of this study is to assess the immunogenicity, reactogenicity and safety of the GSK Biologicals HZ/su candidate vaccine when its first dose is co-administered with Pneumovax 23™ vaccine in adults aged 50 years or older.The impact of HZ/su vaccine on Pneumovax 23™ vaccine immune response will also be evaluated.
Study Details
Timeline
Interventions
2 doses administered intramuscularly (IM) in the deltoid region of the non-dominant arm.
One dose administered intramuscularly (IM) in the deltoid region of the non-dominant arm.