drugset / Trial / NCT02826798

Study to Evaluate Safety, Tolerability, and Immunogenicity of Candidate Human Cytomegalovirus Vaccine in Healthy Adults

NCT02826798 ↗

RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to compare the safety and effectiveness of four different doses of cytomegalovirus vaccines in healthy adults.

Timeline

Start
2016-06-23
Primary completion
2016-09-15
Completion
2017-08-24

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject VBI-1501 Vaccine 1 ug Intramuscular
Subject VBI-1501A Vaccine 0.5 ug Intramuscular
Subject VBI-1501A Vaccine 1 ug Intramuscular
Subject VBI-1501A Vaccine 2 ug Intramuscular