Phase 2 clinical trial in adults previously vaccinated against SARS-CoV-2 in Chile with an initial schedule of two doses of CoronaVacĀ® plus two booster doses with different vaccines. Subjects will randomly receive a third booster dose with Omicron, trivalent, or CoronaVacĀ® vaccine. The humoral immunogenicity against COVID-19 will be compared in subjects that received the Omicron or the Trivalent vaccines with subjects that received CoronaVacĀ® to determine the superiority of the two candidate vaccines versus CoronaVacĀ®. Subjects will be followed for 6 months after the booster dose administration.
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Superiority in humoral immunogenicity of the neutralizing antibodies against the Delta and Omicron variants in response to a booster dose of the trivalent vaccine compared to CoronaVacĀ® in adults previously immunized against SARS-CoV-2.
Timeframe: Up until 6 months after intervention
Superiority in humoral immunogenicity of neutralizing antibodies against the Omicron variant in response to a booster dose with the Omicron vaccine when compared with CoronaVacĀ® in adults previously immunized against SARS-CoV-2.
Timeframe: Up until 6 months after intervention
Non-inferiority of neutralizing antibodies against the Omicron and Delta variants generated by a booster dose of trivalent vaccine when compared to CoronaVacĀ® in adults previously immunized against SARS-CoV-2 in a heterologous schedule.
Timeframe: Up until 6 months after intervention
Non-inferiority of neutralizing antibodies against the Omicron variant generated by a booster dose with Omicron vaccine when compared with CoronaVacĀ® in adults previously immunized against SARS-CoV-2 in a heterologous schedule.
Timeframe: Up until 6 months after intervention