drugset / Trial / NCT05897190

Evaluate the Safety and Immunogenicity of a SARS-CoV-2 mRNA Vaccine Booster

NCT05897190

Phase 1 Completed 60 enrolled Argorna Pharmaceuticals Co., LTD
RandomizedParallel-groupDouble-blindPrevention

Summary

This study is to evaluate the safety and immunogenicity of a SARS-CoV-2 mRNA Vaccine as a heterologous booster dose in adults who completed 2 doses of inactivated vaccination through 12 months in China.

Timeline

Start
2022-05-16
Primary completion
2022-06-13
Completion
2023-05-12

Drugs

EvaluationDrugModalityDoseRoute
Comparator CoronaVac Vaccine Intramuscular
Subject RBMRNA-405 Messenger RNA (mRNA) Intramuscular