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Safety and Immunogenicity of a Candidate Tuberculosis (TB) Vaccine in Adults With TB Disease
This study will assess the safety and immunogenicity of GSK Biologicals' investigational tuberculosis (TB) vaccine (GSK 692342) compared to placebo when administered at 0, 1 months to human immunodeficiency virus (HIV) negative adults who have received treatment for TB disease (denoted TB-treated cohort) or are currently receiving treatment for TB disease (denoted TB-treatment cohort). For comparative purposes, subjects who have never had TB disease (denoted TB-naïve cohort) will also be enrolled.
Details
| Lead sponsor | GlaxoSmithKline |
|---|---|
| Phase | PHASE2 |
| Status | TERMINATED |
| Enrolment | 142 |
| Start date | Mon Nov 14 2011 00:00:00 GMT+0000 (Coordinated Universal Time) |
| Completion | Thu Apr 10 2014 00:00:00 GMT+0000 (Coordinated Universal Time) |
Conditions
- Tuberculosis
Interventions
- GSK Biologicals' investigational TB vaccine GSK 692342
- Placebo
Countries
Taiwan, Estonia