This is a Phase I/IIa Study to Assess the Safety, Tolerability and Explore the Immunogenicity of EG-COVII in Healthy Adult Volunteers
Subjects will undergo a Screening period beginning up to 2 weeks prior to enrollment, the vaccinations will be administered on week 0 and week 3, pre- and post-dose assessment, follow-up visits, and an end of study (EOS) or early termination (ET) visit (as applicable).
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
PREVENTION
Masking
NONE
Enrollment
40
EG-COVII is a bivalent vaccine to prevent SARS-CoV-2 infection against wild type and Omicron variants
Nucleus Network Pty Ltd- Melbourne
Melbourne, Victoria, Australia
Safety and tolerability of EG-COVII in healthy adult volunteers
Number of participants with adverse events (AEs) Number of participants with abnormal clinical laboratory results (hematology /chemistry /urinalysis) Number of participants with abnormal vital sign Number of participants with abnormal physical examination results
Time frame: 7 weeks follow up
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