Clinical Trial Results:
A phase II, open, randomised, comparative study to evaluate the immunogenicity and safety of GlaxoSmithKline's (GSK) Biologicals' measles-mumps-rubella-varicella candidate vaccine (MeMuRu-OKA) and GSK Biologicals' measles-mumps-rubella vaccine (Priorix) co-administered in separate injections with GSK Biologicals' varicella vaccine (Varilrix) when given in healthy children who previously received a first dose of an MMR vaccine.
Summary
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EudraCT number |
2005-006065-14 |
Trial protocol |
DE IT |
Global completion date |
24 Nov 2006
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Paediatric regulatory details
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Is the trial part of an agreed EMA paediatric investigation plan? |
No
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Is the trial in scope of article 45 of Regulation (EC) No 1901/2006? |
Yes
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Is the trial in scope of article 46 of Regulation (EC) No 1901/2006? |
No
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Results information
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Results version number |
v1(current) |
This version publication date |
23 Sep 2018
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First version publication date |
23 Sep 2018
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Other versions |
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Summary report(s) |
105908-Clinical-Study-Result-Summary |
Note: The legislation allows summary attachments to be posted instead of the full dataset for this trial. Refer to Commission Guideline 2012/C 302/03
for further information.