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Clinical Trial Summary

The purpose of the study is to evaluate the safety and reactogenicity of candidate gD vaccine, with or without MPL, in HSV-seropositive subjects. The immune response elicited in these subjects will also be evaluated.


Clinical Trial Description

At the time of conduct of this study, the sponsor GlaxoSmithKline was known by its former name SmithKline Beecham ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00698893
Study type Interventional
Source GlaxoSmithKline
Contact
Status Completed
Phase Phase 1
Start date May 1, 1992
Completion date July 1, 1992

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