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Clinical Trial Summary

Evaluate the safety and immunogenicity of the trivalent group B streptococcus vaccine in healthy pregnant women. The study will also evaluate the levels of GBS serotype-specific antibodies in infants, placental transfer from the pregnant women to the infant and levels of antibodies in the breast milk.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02046148
Study type Interventional
Source GlaxoSmithKline
Contact
Status Completed
Phase Phase 2
Start date March 18, 2014
Completion date March 26, 2016

See also
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Completed NCT00920530 - Real-Time PCR for the Detection of Vaginal Group B Streptococcus Carriage: a Medico-Economic Study N/A
Completed NCT05005169 - CCA of SGB PCR Versus SGB Culture at 35-38 SA in the Optimization of Intrapartum Antibiotic Prophylaxis N/A
Completed NCT02690181 - Extension Study to Evaluate the Immunogenicity and Safety of the Second Dose of GBS Trivalent Vaccine in Healthy Non-Pregnant Subjects. Phase 2
Completed NCT01888471 - Feasibility Study for Identifying Anti Capsular Antibody Protection Against Invasive Group B Streptococcus (GBS) Disease in Newborns of 0-6 Days Age (Early Onset Disease [EOD]) as Well as Among Infants of 7-90 Days Age (Late Onset Disease [LOD]) N/A