CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 110 enrolled
Drug / intervention
GSK's candidate Mycobacterium tuberculosis vaccine 692342 +3 morebiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00397943
NCT00397943Phase 2Completed

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

GlaxoSmithKline·interventional·Posted Nov 10, 2006·Updated Jun 19, 2019

In Brief

A Phase 2 clinical trial evaluating GSK's candidate Mycobacterium tuberculosis vaccine 692342, Comparator vaccine with recombinant Mycobacterium tuberculosis antigen and adjuvant system, and 2 other interventions for Tuberculosis. Completed, enrolled 110 participants across 1 site.

Detailed Summary

This study will assess the safety and immunogenicity of 2 different formulations of tuberculosis vaccine GSK692342 in healthy adults.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsTuberculosis
CountriesBelgium
Collaborators--

Timeline

Phase 2CompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedNov 10, 2006
Enrollment StartNov 15, 2006
Primary CompletionDec 1, 2009
TodayJul 2, 2026
Enrollment to primary: 3.0 yearsPosted 19.6 years ago

Interventions

GSK's candidate Mycobacterium tuberculosis vaccine 692342biological

Intramuscular injection, 2 doses at 0, 1 month

Comparator vaccine with recombinant Mycobacterium tuberculosis antigen and adjuvant systembiological

Intramuscular injection, 2 doses at 0, 1 month

Comparator vaccine with recombinant Mycobacterium tuberculosis antigen and physiological salinebiological

Intramuscular injection, 2 doses at 0, 1 month

Control vaccine with the adjuvant system.biological

Intramuscular injection, 2 doses at 0, 1 month