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Clinical Trial Summary

The purpose of this study is to estimate the incidence of Cytomegalovirus (CMV) secondary infections (re-infections/re-activations) and the incidence of CMV primary infections in adolescent females.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01691820
Study type Interventional
Source GlaxoSmithKline
Contact
Status Completed
Phase N/A
Start date October 5, 2012
Completion date April 8, 2017

See also
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Completed NCT01357915 - Evaluation of the Long-term Persistence of GlaxoSmithKline (GSK) Biologicals' Candidate Cytomegalovirus (CMV) Vaccine N/A
Completed NCT00435396 - Study to Evaluate Safety and Immunogenicity of the GSK Bio CMV Vaccine in CMV-seronegative Healthy Male Adult Subjects Phase 1
Completed NCT01251744 - Study of the Transmission of Cytomegalovirus (CMV) Infection From Mother to Foetus N/A