drugset / Trial / NCT06167915
Safety and Immunogenicity of Recombinant COVID-19 Trivalent Protein Vaccine (CHO Cell)LYB002V14 in Booster Vaccination
Phase 1
Unknown
120 enrolled
Guangzhou Patronus Biotech Co., Ltd.
Yantai Patronus Biotech Co., Ltd. · collab
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | LYB002V14 | Vaccine | 30 ug | Intramuscular |
| Subject | LYB002V14 | Vaccine | 60 ug | Intramuscular |