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Clinical Trial Summary

The purpose of the study is to compare, in healthy HSV seronegative and HSV seropositive subjects, the humoral and cellular immune response of herpes simplex candidate vaccines containing gD from two different cell lines and using gD-Alum as control.


Clinical Trial Description

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


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT00698490
Study type Interventional
Source GlaxoSmithKline
Contact
Status Completed
Phase Phase 1/Phase 2
Start date August 1995
Completion date January 1997

See also
  Status Clinical Trial Phase
Completed NCT00697567 - Evaluation of Immunogenicity, Reactogenicity and Safety of Herpes Simplex (gD) Candidate Vaccine With/Without Adjuvant Phase 2