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Clinical Trial Summary

The purpose of this study is to assess immunogenicity and safety of GSK Biologicals' HZ vaccine when its first dose is co-administered with a pneumococcal polysaccharide conjugate vaccine (Prevenar13) in adults aged ≥50 YOA, as compared to the control group where the two HZ/su doses are administered subsequent to Prevenar13.


Clinical Trial Description

Following the initial approval of the GlaxoSmithKline (GSK) Biologicals' HZ/su vaccine, the protocol was amended to indicate that the trademark is Shingrix. In addition, the term "candidate" vaccine has been replaced by "study" vaccine throughout the protocol. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03439657
Study type Interventional
Source GlaxoSmithKline
Contact
Status Completed
Phase Phase 3
Start date April 12, 2018
Completion date March 3, 2020

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