Last updated on November 2019

Immunogenicity and Safety Study of GSK Biologicals' Herpes Zoster Vaccine GSK1437173A When Co-administered With Prevenar13 in Adults Aged 50 Years and Older


Brief description of study

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.

Detailed Study 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 In addition, the term "candidate" vaccine has been replaced by "study" vaccine throughout the protocol.

Clinical Study Identifier: NCT03439657

Recruitment Status: Closed


Brief Description Eligibility Contact Research Team


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