Last updated on February 2019

RSV Investigational Vaccine in RSV-seropositive Infants Aged 12 to 23 Months


Brief description of study

The purpose of this study is to evaluate the safety, reactogenicity and immunogenicity of the respiratory syncytial virus (RSV) candidate vaccine when first administered via intramuscular (IM) injection according to a 0, 1-month schedule to RSV-seropositive infants aged 12 to 23 months.

Detailed Study Description

The RSV PED-002 study, designed to evaluate the safety, reactogenicity and immunogenicity of the RSV candidate vaccine when administered in 3 sequential doses to seropositive infants aged 12 to 23 months, will be conducted in an observer-blind manner in Epoch 1 and single-blinded in Epoch 2.

Clinical Study Identifier: NCT02927873

Contact Investigators or Research Sites near you

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GSK Investigational Site

Panama, Panama

Recruitment Status: Closed


Brief Description Eligibility Contact Research Team


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