Study of AERAS 422 in Healthy Adults

NCT01340820 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2012-08-16

No results posted yet for this study

Summary

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

Conditions

Interventions

DRUG

AERAS-422

rBCG

DRUG

BCG Tice

1-8 x 10\^5 CFU

Sponsors & Collaborators

  • Aeras

    lead OTHER

Principal Investigators

  • Daniel Hoft, MD · St. Louis University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-12-31
Primary Completion
2012-02-29
Completion
2012-05-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01340820 on ClinicalTrials.gov