Clinical trial

Safety and Immunogenicity of 2 Formulations of Tuberculosis Vaccine GSK692342…

NCT00397943 · GlaxoSmithKline, Industry · Completed

Key facts

NCT number NCT00397943
Title Safety and Immunogenicity of 2 Formulations of Tuberculosis Vaccine GSK692342 Given at 0,1 Months to Healthy Adults
Official title Safety, Reactogenicity & Immunogenicity of 2 Formulations of Tuberculosis Vaccine GSK692342 Administered Intramuscularly According to a Schedule of 0, 1 Month, to Healthy Adults Aged 18 to 50 Years
Lead sponsor GlaxoSmithKline, Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Tuberculosis
Intervention type Biological
Interventions GSK's candidate Mycobacterium tuberculosis vaccine 692342, Comparator vaccine with recombinant Mycobacterium tuberculosis antigen and adjuvant system, Comparator vaccine with recombinant Mycobacterium tuberculosis antigen and physiological saline, Control vaccine with the adjuvant system.
Enrollment 110
Start date Nov 15, 2006
Primary completion Dec 1, 2009
Completion Dec 1, 2009
First posted Nov 10, 2006
Last update posted Jun 19, 2019
Countries Belgium

At a glance

  • 1–9 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About ClinicalTrials.gov studies

ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.

Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

Browse all ClinicalTrials.gov studies