drugset / Trial / NCT04478656

Safety and Immunogenicity of BBV121

NCT04478656 ↗

Phase 1 Completed 48 enrolled Bharat Biotech International Limited
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

EvaluationDrugModalityDoseRoute
Subject BBV121 Vaccine 2.5 ug Intramuscular
Subject BBV121 Vaccine 5 ug Intramuscular
Subject BBV121 Vaccine 10 ug Intramuscular