Study of AERAS 422 in Healthy Adults

The purpose of this study is to evaluate the safety and immunogenicity of AERAS-422 in healthy, BCG-naïve adults.

This is a Phase I, randomized, controlled, double-blind, dose-escalation study of AERAS-422. This study will be conducted in 24 HIV-negative, healthy adults who are BCG-naïve and negative for prior exposure to Mtb at enrollment. The study will be conducted at one or more clinical research sites in the United States.

AERAS-422 will be administered on Study Day 0 as a single 0.1 mL intradermal (ID) injection containing either \>= 10\^5 to \<10\^6 CFU (low-dose) or \>=10\^6 CFU (high-dose). BCG Tice® will be used as an active control for AERAS-422 and will be administered as a single 0.1 mL ID injection containing 1-8 x 10\^5 CFU on Study Day 0.