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

SARS-CoV-2 Clinical Trial

Official title:

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

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06167915
• Other study ID #: LYB002V14/CT-CHN-101
• Status: Not yet recruiting
• Phase: Phase 1
• Start date: December 26, 2023
• Est. completion date: December 31, 2024

Study information

• Verified date: December 2023
• Source: Guangzhou Patronus Biotech Co., Ltd.
• Contact: Qin Yu, Master
• Phone: 18980602109
• Email: 908929936[@]qq.com
• Is FDA regulated: No
• Study type: Interventional

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）.

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.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 120
• Est. completion date: December 31, 2024
• Est. primary completion date: December 26, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

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: ?Any acute diseases or acute attacks of chronic diseases within 7 days prior to enrolment. ?Congenital malformations or developmental disorders, genetic defects, severe malnutrition, etc. ?Congenital 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. ?Currently suffering from or diagnosed with infectious diseases, or positive screening results for human immunodeficiency virus antibody. ?History or family history of neurological disorders (convulsions, epilepsy, encephalopathy, etc.) or psychiatric disorders. ?Asplenia, or functional asplenia. ?Presence 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. ?Contraindications to IM injections and blood draws, such as coagulation disorders, thrombotic or bleeding disorders, or conditions that needs continuous anticoagulant usage. ?Hypertension 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.

Related Conditions & MeSH terms

• COVID-19
• COVID-19 Vaccine
• SARS-CoV-2

Intervention

Biological:
• 30µg dose of LYB002V14
30µg dose of LYB002V14 vaccine IM, on day 0
• 60µg dose of LYB002V14
60µg dose of LYB002V14 vaccine IM, on day 0
• placebo
placebo IM, on day 0

Locations

Country	Name	City	State
China	West China Second University Hospital, Sichuan University	Chengdu	Sichuan

Sponsors (2)

Lead Sponsor	Collaborator
Guangzhou Patronus Biotech Co., Ltd.	Yantai Patronus Biotech Co., Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	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	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
Secondary	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
Secondary	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
Secondary	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
Secondary	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
Secondary	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
Secondary	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-? and IL-4 cytokine levels at baseline, Day 14 and Month 6 after booster vaccination.	Day 14 and Month 6