drugset / Trial / NCT04478656
Safety and Immunogenicity of BBV121
RandomizedParallel-groupDouble-blindPrevention
Summary
To evaluate the safety, tolerability, and immunogenicity of two-doses of three-sequentially escalating cohort (2.5 µg, 5 µg and 10 µg) of BBV121 (purified inactivated adsorbed Zika virus vaccine) compared with Placebo (Alum). The investigational product is administered intramuscularly on Day 0 and 28 with safety and immunogenicity testing on Day 0, 28 and 56, and Month 6, 9 and 12
Timeline
- Start
- 2017-06-03
- Primary completion
- 2017-11-15
- Completion
- 2018-11-15
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | BBV121 | Vaccine | 2.5 ug | Intramuscular |
| Subject | BBV121 | Vaccine | 5 ug | Intramuscular |
| Subject | BBV121 | Vaccine | 10 ug | Intramuscular |