Phase I/II study to determine safety, tolerance and immunogenicity of EuCorVac-19, a recombinant protein vaccine, for the prevention of COVID-19 in healthy adults
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Enrollment
279
Two intramuscular doses (0.5mL per dose) at 3-week interval
Two intramuscular doses (0.5mL per dose) at 3-week interval
The Catholic University of Eunpyeong St.Mary's Hospital
Seoul, South Korea
Immediate AEs
Time frame: within 30 minutes after each IP dosing
Solicited local and systemic AEs
Time frame: for 7 days after each IP dosing
Unsolicited AEs
Time frame: within 28 days after the last IP dosing
SAEs
Time frame: within 52 weeks after the last IP dosing
AESIs
Time frame: within 52 weeks after the last IP dosing
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