IGRA Epid Study
A multi-country, epidemiologic study to assess the interferon gamma release assay (IGRA) positivity, and to build capacity to conduct a tuberculosis (TB) vaccine efficacy study, in populations with a high TB disease burden
Information
This study will be conducted to assess the proportion of IGRA positivity based on study location and to build capacity for conducting a pivotal phase 3 TB vaccine efficacy study.
The study will take place at 42 sites across 14 countries, including Indonesia, South Africa, Kenya, Gambia, Zambia, Uganda, Peru, Mozambique, Brazil, Congo, Vietnam, the Philippines, India, and Bangladesh.
The target number of participants is 8,000 worldwide, with 160 participants per site.
Bill and Melinda Gates Foundation – Medical Reseearch Institute
Type of Study
Collabolator
Observational Study
Tuberculosis
Background
MTB infection causing TB disease is one of the top 10 causes of death worldwide. The most effective contribution to controlling TB is vaccination. BCG is the only licensed vaccine; however, this vaccine does not provide substantial protection against pulmonary TB in adults infected with MTB. GlaxoSmithKline Biologicals, SA (GSK) has developed M72/AS01E, a TB vaccine candidate to protect against TB in adolescents and adults. The IGRA study will help refine the sample size and duration required for phase 3 studies.
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Head Office Address
Jl. Balai Pustaka Barat 358E
Rawamangun, Pulo Gadung
Jakarta Timur, 13220
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Corresponding Address
Jalan Pegambiran No. 37 lantai 2,
Rawamangun, Pulo Gadung
Jakarta Timur, 13220