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

A Randomized, Blinded, Placebo-Controlled, Dose Escalation Phase 1 Trial of Recombinant COVID-19 Trivalent (XBB.1+BQ.1.1+Prototype) Protein Vaccine （CHO Cell）（LYB002V14） in Booster Vaccination in Participants Aged 18 Years Old and Above

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）.

Study Overview

• Status: Not yet recruiting
• Conditions: SARS-CoV-2; COVID-19 Vaccine
• Intervention / Treatment: Biological: 30μg dose of LYB002V14; Biological: 60μg dose of LYB002V14; Biological: placebo

Detailed 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 Type: Interventional
• Enrollment (Estimated): 120
• Phase: Phase 1

Contacts and Locations

• Study Contact: Name: Qin Yu, Master; Phone Number: 18980602109; Email: 908929936@qq.com

Study Locations

• China
  • Sichuan
    • Chengdu, Sichuan, China
      • West China Second University Hospital, Sichuan University
      • Contact: Qin Yu, Master; Phone Number: 18980602109; Email: 908929936@qq.com

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: Yes

Description

Inclusion Criteria:

1. Subjects aged 18 years and above when screening.
2. Participate voluntarily and sign an informed consent form and have the ability to understand research procedures.
3. Negative SARS-CoV-2 nucleic acid test and SARS-CoV-2 IgM test.
4. Axillary body temperature is less than 37.3 degree centigrade on the day of enrollment.
5. Without a history of SARS-CoV-2 infection or known SARS-CoV-2 infection more than 3 months prior to screening.
6. Fertile women take effective contraceptive measures 1 month before enrollment; Fertile women (except those received hysterectomy, bilateral oophorectomy, tubal ligation/salpingectomy) and men of childbearing potential voluntarily agree to take effective contraceptive measures from screening to 3 months after vaccination and without a plan of pregnancy and germ cell donation.

Exclusion Criteria:

1. Have a known allergy, hypersensitivity, or intolerance to the planned investigational vaccine including any excipients of the vaccine. Have a known anaphylactic shock and other serious adverse events to other vaccine.
2. Have a known history of SARS and MERS.
3. Administration of antipyretics, painkillers or anti-allergy drugs within 24 hours prior to enrolment.
4. Receipt of subunit and/or inactivated vaccine within 7 days prior to vaccination or receipt of any live attenuated vaccine within 14 days prior to vaccination.
5. History of SARS-CoV-2 vaccination within 3 months prior to enrollment; Participants who received any immunoglobulin or blood products in the previous 3 months before enrollment, or plan to receive similar products during the study.
6. Participants with the following diseases: ①Any acute diseases or acute attacks of chronic diseases within 7 days prior to enrolment. ②Congenital malformations or developmental disorders, genetic defects, severe malnutrition, etc. ③Congenital or acquired immunodeficiency or autoimmune disease, or long-term receipt (>14 immunosuppressive agents within the past 6 months with exception of inhaled or topical steroids, or short-term use （≤14 consecutive days） of oral corticosteroids. ④Currently suffering from or diagnosed with infectious diseases, or positive screening results for human immunodeficiency virus antibody. ⑤History or family history of neurological disorders (convulsions, epilepsy, encephalopathy, etc.) or psychiatric disorders. ⑥Asplenia, or functional asplenia. ⑦Presence of severe, uncontrollable or hospitalized cardiovascular diseases, diabetes, blood and lymphatic diseases, immune diseases, liver and kidney diseases, respiratory diseases, metabolic and skeletal diseases, or malignant tumors. ⑧Contraindications to IM injections and blood draws, such as coagulation disorders, thrombotic or bleeding disorders, or conditions that needs continuous anticoagulant usage. ⑨Hypertension not controlled by medication (on-site measurement: systolic blood pressure ≥ 160mmHg and / or diastolic blood pressure ≥ 100mmHg).
7. Have a history of major surgery within 3 months before enrollment （based on the judgment of the researchers）, or has not yet fully recovered from the surgery, or has a major surgical plan during the study.
8. Those participating or planning to participate in other clinical trials during the study period.
9. Those unsuitable for participating in the clinical trial as determined by the investigator because of other abnormalities that are likely to confuse or confound the study results, or non-conformance with the maximal benefits of the participants.
10. Exclusion criteria for selected populations: those who are pregnant or breast-feeding or women of childbearing potential have a positive pregnancy test prior to vaccination.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Prevention
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Triple

Number of Arms

3

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Low dose vaccine group; 30μg dose of LYB002V14 vaccine IM, on day 0.	Biological: 30μg dose of LYB002V14; 30μg dose of LYB002V14 vaccine IM, on day 0
Experimental: High dose vaccine group; 60μg dose of LYB002V14 vaccine IM, on day 0.	Biological: 60μg dose of LYB002V14; 60μg dose of LYB002V14 vaccine IM, on day 0
Placebo Comparator: Placebo group; placebo IM, on day 0.	Biological: placebo; placebo IM, on day 0

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Adverse events and adverse reactions	Statistical description of solicited and unsolicited adverse events （AEs） will be listed. Frequencies and percentages of AEs, including overall AEs, AEs related to vaccination, AEs classified as grade 3 or worse, AEs classified as grade 3 or worse that related to vaccination, AEs leading to participant's withdrawal, AEs leading to participant's withdrawal that related to vaccination will be presented. Fisher's exact test will be used to compare the differences between the groups.	Day 0 to Day 7

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Laboratory test and vital signs related adverse events.	Indicator of Laboratory test and vital signs related adverse events will be evaluated with three days after booster vaccination.	Day 0 to Day 3
Adverse events and adverse reactions	Statistical description of solicited and unsolicited adverse events （AEs） will be listed. Frequencies and percentages of AEs, including overall AEs, AEs related to vaccination, AEs classified as grade 3 or worse, AEs classified as grade 3 or worse that related to vaccination, AEs leading to participant's withdrawal, AEs leading to participant's withdrawal that related to vaccination will be presented. Fisher's exact test will be used to compare the differences between the groups.	Day 0 to Day 28
Serious Adverse Events （SAEs） and Adverse Events of Special Interest （AESI）	Statistical description of Serious Adverse Events （SAEs） and Adverse Events of Special Interest （AESI） will be listed. Frequencies and percentages of SAEs and AESI, related to vaccination will be followed during the whole observation.	Day 0 to Month 12
Geometric mean titer （GMT）, Geometric Mean Fold Rise （GMFR） and seroconversion rate （SCR） of neutralizing antibodies （nAb） against variants of concern circulating during the trial.	The Seroconversion （SCRs） with Clopper-Pearson 95% CIs of neutralizing antibodies （Nabs） against circulating VOCs using Vesicular stomatitis virus （VSV）-based pseudovirus neutralizing assays, at Day 14、Day 28、Month 3 and Month 6 after booster immunization will be calculated for each group, compared with the baseline.	Day 14、Day 28、Month 3 and Month 6
GMT, GMFR and SCR of nAb against Omicron subvariant （XBB）	The Seroconversion （SCRs） with Clopper-Pearson 95% CIs of neutralizing antibodies （Nabs） against Omicron subvariant （XBB） using Vesicular stomatitis virus （VSV）-based pseudovirus neutralizing assays, at Day 14、Day 28、Month 3 and Month 6 after booster immunization will be calculated for each group, compared with the baseline.	Day 14、Day 28、Month 3 and Month 6
Geometric Mean Concentration （GMC）, GMFR and SCR of SARS-CoV-2 Spike protein binding antibody.	Geometric Mean Concentration（GMC）, GMFR and SCR with Clopper-Pearson 95% CIs of S protein-binding antibodies using ELISA assays, at baseline, at Day 14、Day 28、Month 3 and Month 6 after the booster immunization will be calculated for each group, compared with the baseline.	Day 14、Day 28、Month 3 and Month 6
Th1 and Th2 cytokine responses	The counts of spot forming cells （SFCs） per 3×10^5 peripheral blood mononuclear cells （PBMCs） of Cellular immunity RBD-specific IFN-γ and IL-4 cytokine levels at baseline, Day 14 and Month 6 after booster vaccination.	Day 14 and Month 6

Collaborators and Investigators

• Sponsor: Guangzhou Patronus Biotech Co., Ltd.
• Collaborators: Yantai Patronus Biotech Co., Ltd.
• Investigators: Principal Investigator: Qin Yu, Master, West China Second University Hospital

Study record dates

Study Major Dates

• Study Start (Estimated): December 26, 2023
• Primary Completion (Estimated): December 26, 2024
• Study Completion (Estimated): December 31, 2024

Study Registration Dates

• First Submitted: December 11, 2023
• First Submitted That Met QC Criteria: December 11, 2023
• First Posted (Actual): December 13, 2023

Study Record Updates

• Last Update Posted (Actual): December 26, 2023
• Last Update Submitted That Met QC Criteria: December 18, 2023
• Last Verified: December 1, 2023

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Coronavirus Infections; Coronaviridae Infections; Nidovirales Infections; RNA Virus Infections; Virus Diseases; Infections; Respiratory Tract Infections; Respiratory Tract Diseases; Pneumonia, Viral; Pneumonia; Lung Diseases; COVID-19
• Other Study ID Numbers: LYB002V14/CT-CHN-101

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No