drugset / Trial / NCT00717834

Safety and Immunogenicity Study of a Ross River Virus (RRV) Vaccine

NCT00717834 ↗

Phase 1/2 Completed 400 enrolled Alachua Government Services, Inc.
RandomizedParallel-groupOpen-labelPrevention

Summary

The primary objective of this study is to assess the safety and tolerability of the Ross River Virus (RRV) Vaccine in a healthy young adult population. Other objectives of this study are to assess the immunogenicity of the RRV Vaccine in a healthy young adult population and to identify the optimal dose level of the RRV Vaccine in a healthy young adult population.

Timeline

Start
2008-06
Primary completion
2008-10
Completion
2009-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Al(OH)3 Unknown — Intramuscular
Subject Ross River Virus (RRV) Vaccine Vaccine 1.25 ug Intramuscular
Subject Ross River Virus (RRV) Vaccine Vaccine 2.5 ug Intramuscular
Subject Ross River Virus (RRV) Vaccine Vaccine 5 ug Intramuscular
Subject Ross River Virus (RRV) Vaccine Vaccine 10 ug Intramuscular

Indications