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Clinical Trial 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).


Clinical Trial Description

The study is a randomized, blinded and dose escalation Phase I clinical trial. It will evaluate the safety and immunogenicity of 2 dose levels of recombinant COVID-19 trivalent (XBB.1+BQ.1.1+Prototype) protein vaccine (CHO Cell)(LYB002V14)in booster vaccination. Approximately 120 participants aged 18 years and older will be enrolled in this study. The subjects in each dose group will randomly receive an intramuscular (IM) injection of experimental vaccine or placebo on Days 0 in the deltoid muscle at 2:1 and will be followed through 12 months post vaccination. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06167915
Study type Interventional
Source Guangzhou Patronus Biotech Co., Ltd.
Contact Qin Yu, Master
Phone 18980602109
Email 908929936@qq.com
Status Not yet recruiting
Phase Phase 1
Start date December 26, 2023
Completion date December 31, 2024

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