drugset / Trial / NCT06167915

Safety and Immunogenicity of Recombinant COVID-19 Trivalent Protein Vaccine (CHO Cell)LYB002V14 in Booster Vaccination

NCT06167915 ↗

RandomizedParallel-groupTriple-blindPrevention

Summary

This is a randomized, blinded, and dose escalation phase I trial in males and non-pregnant females, starting at 18 years of age, inclusive, who are in good health and meet all eligibility criteria. This clinical trial is designed to assess the safety and immunogenicity of Recombinant COVID-19 Trivalent (XBB.1+BQ.1.1+Prototype) Protein Vaccine (CHO Cell)(LYB002V14).

Timeline

Start
2023-12-26
Primary completion
2024-12-26
Completion
2024-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject LYB002V14 Vaccine 30 ug Intramuscular
Subject LYB002V14 Vaccine 60 ug Intramuscular