drugset / Trial / NCT02699099
Immunogenicity and Safety Study of GSK Biologicals' Candidate Malaria Vaccine Given at 6, 7.5 and 9 Months of Age in Co-administration With Measles, Rubella and Yellow Fever (YF) Vaccines Followed by a Booster of the Malaria Vaccine.
RandomizedParallel-groupOpen-labelPrevention
Summary
The purpose of this study is to assess the immunogenicity, safety, and reactogenicity of the SB257049 candidate malaria vaccine when co-administered with Vitamin A, measles, rubella and yellow fever vaccines to children aged 6 months at the first vaccination.
Timeline
- Start
- 2017-05-10
- Primary completion
- 2018-03-14
- Completion
- 2020-10-07
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | SB257049 | Vaccine | — | Intramuscular |
| Background | MR-Vac | Vaccine | — | Subcutaneous |
| Background | Yellow Fever Vaccine | Vaccine | — | Intramuscular |