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Clinical Trial Summary

The purpose of this study is to evaluate the immunogenicity and safety of GSK Biologicals' HZ/su vaccine in adults with solid tumours undergoing chemotherapy.


Clinical Trial Description

The study will be randomised into two groups based on the vaccination schedule in relation to the start of a chemotherapy cycle: - The OnChemo group receives their first HZ/su vaccination at the start of a chemotherapy cycle, - The PreChemo group receives their first HZ/su vaccination at least 10 days before the start of a chemotherapy cycle. The protocol summary has been updated following Protocol Amendment 2, August 2014, leading to the increase of the enrolment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01798056
Study type Interventional
Source GlaxoSmithKline
Contact
Status Completed
Phase Phase 3
Start date March 6, 2013
Completion date May 20, 2016

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