drugset / Trial / NCT02074956

A Phase I Study to Evaluate Safety and Immunogenicity of AERAS 404 Administered in Adults

NCT02074956

Phase 1 Completed 60 enrolled Aeras Statens Serum Institut · collab
RandomizedParallel-groupQuadruple-blindPrevention

Summary

This Phase I study will be conducted as a randomized, double-blind, dose-escalation study in five groups of healthy adult male and female subjects who are BCG-vaccinated, HIV-negative, and have no evidence of tuberculosis infection. Since BCG-vaccinated individuals are the target population for which AERAS 404 might be indicated, AERAS 404 will be administered to individuals already vaccinated with BCG

Timeline

Start
2008-05
Primary completion
2009-10
Completion
2009-10

Drugs

EvaluationDrugModalityDoseRoute
Subject AERAS-404 Vaccine 5 ug Intramuscular
Subject AERAS-404 Vaccine 15 ug Intramuscular
Subject AERAS-404 Vaccine 50 ug Intramuscular
Subject AERAS-404 Vaccine 150 ug Intramuscular
Subject IC31 Other / unclassified 0.0001 mmol Intramuscular
Subject IC31 Other / unclassified 0.0005 mmol Intramuscular

Indications