drugset / Trial / NCT05270954

Safety, Tolerability and Immunogenicity of Recombinant COVID-19 Vaccine Betuvax-CoV-2

NCT05270954 ↗

RandomizedParallel-groupTriple-blindPrevention

Summary

Randomized, double-blind, multicenter parallel-group clinical study of safety, tolerability and immunogenicity of the Betuvax-CoV-2 vaccine. The aim of this study is to investigate the safety, tolerability and immunogenicity of the Betuvax-CoV-2 Recombinant vaccine for the prevention of coronavirus infection caused by the SARS-CoV-2 virus, suspension for intramuscular administration, 10 μg/ml and 40 μg/ml (Ltd. Institute of New Medical Technologies, Russia) in healthy adult volunteers, aged 18 to 60 (inclusive).

Timeline

Start
2021-10-14
Primary completion
2022-04-25
Completion
2022-07-24

Drugs

EvaluationDrugModalityDoseRoute
Comparator Betuvax-CoV-2 Vaccine 5 ug Intramuscular
Comparator Betuvax-CoV-2 Vaccine 20 ug Intramuscular

Indications