Immunogenicity，Safety and Cross - Immune Response With Mutant Strains of a Third Dose of an Inactivated COVID-19 Vaccine

COVID-19 Clinical Trial

Official title:

Immunogenicity，Safety and Cross - Immune Response With Mutant Strains of the Third Dose Using Inactivated COVID-19 Vaccine in Population Aged 18 Years and Above

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT05329038
• Other study ID #: PRO-nCOV-MA4009-SD
• Status: Active, not recruiting
• Phase: Phase 4
• Start date: April 19, 2022
• Est. completion date: February 20, 2024

Study information

• Verified date: November 2023
• Source: Sinovac Biotech Co., Ltd
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a phase Ⅳ follow-up clinical trial based on the previous Phase Ⅳ clinical trial of an inactivated COVID-19 vaccine (CoronaVac) manufactured by Sinovac Life Sciences Co., Ltd.The purpose of this study is to evaluate the immunogenicity,safety and cross-immune response of booster immunization using COVID-19 vaccine,to compare the similarities and differences of immune responses between primary immunization and booster immunization and to detect antibody against hepatitis A and evaluate the immune persistence of the one dose immunization schedule of hepatitis A vaccine in healthy population aged 18 years and older.

Description:

This study is a phase 4 clinical trial to evaluate the immunogenicity,safety and cross-immune response of booster immunization using COVID-19 vaccine，to compare the similarities and differences of immune responses between primary immunization and booster immunization and to detect antibody against hepatitis A and evaluate the immune persistence of the one dose immunization schedule of hepatitis A vaccine in healthy population aged 18 years and older. The experimental vaccine is manufactured by Sinovac Life Sciences Co., Ltd.. A total of 180 healthy subjects received two dose of inactivated COVID-19 vaccine (CoronaVac) based on primary immunization in previous Phase Ⅳ clinical trial will be enrolled, including 90 adults aged 18-59 years and 90 elderly elderly aged 60 years and older.Subjects in each age group will receive the booster immunization of CoronaVac(the third dose) and will be collected blood sample before booster immunization and 14 days after booster immunization.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 180
• Est. completion date: February 20, 2024
• Est. primary completion date: June 19, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Participated in the clinical studies on the safety and immunogenicity of Inactivated COVID-19 Vaccine combined immunization with 23-valent pneumococcal polysaccharide vaccine in Rushan city, Shandong Province from July to October 2021;

• The interval between complete immunization with two doses of COVID-19 vaccine is 6-8 months;

• Subjects will be willing to participate in the study and follow the study procedure to collect venous blood;

• Proven legal identity;

Exclusion Criteria:

• History of asthma, history of allergy to the vaccine or vaccine components,or serious adverse reactions to the vaccine, such as urticaria, dyspnea,and angioedema;

• Severe neurological disease (epilepsy, convulsions or convulsions) or mental illness;

• Fever at the time of vaccination, or acute onset of chronic disease, or uncontrolled severe chronic disease, or acute disease;

• Pregnancy or lactation;

• Receipt of attenuated live vaccines in the past 14 days;

• Receipt of inactivated or subunit vaccines in the past 7 days

• According to the investigator's judgment, the subject has any other factors that are not suitable for participating in the clinical trial.

Related Conditions & MeSH terms

• COVID-19

Intervention

Biological:
• Inactivated COVID-19 Vaccine
600SU inactivated virus in 0·5 mL of aluminium hydroxide solution per injection

Locations

Country	Name	City	State
China	Rushan City Center for Disease Control and Prevention	Weihai	Shandong

Sponsors (1)

Lead Sponsor	Collaborator
Sinovac Life Sciences Co., Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Seroconversion rate of neutralizing antibody against Prototype SARS-CoV-2	The seroconversion rate of neutralizing antibody against Prototype SARS-CoV-2 at 14 days after the booster immunization of inactivated COVID-19 vaccine.	14 days after the booster immunization of inactivated COVID-19 vaccine
Secondary	Seropositive rate of neutralizing antibody against Prototype SARS-CoV-2	The seropositive rate of neutralizing antibody against Prototype SARS-CoV-2 at 14 days after the booster immunization of inactivated COVID-19 vaccine.	14 days after the booster immunization of inactivated COVID-19 vaccine
Secondary	GMT of neutralizing antibody against Prototype SARS-CoV-2	The GMT of neutralizing antibody against Prototype SARS-CoV-2 at 14 days after the booster immunization of inactivated COVID-19 vaccine.	14 days after the booster immunization of inactivated COVID-19 vaccine
Secondary	GMI of neutralizing antibody against Prototype SARS-CoV-2	The GMI of neutralizing antibody against Prototype SARS-CoV-2 at 14 days after the booster immunization of inactivated COVID-19 vaccine.	14 days after the booster immunization of inactivated COVID-19 vaccine
Secondary	Seroconversion rate of neutralizing antibody against SARS-CoV-2 strains	The seroconversion rate of neutralizing antibody against SARS-CoV-2 strains at 14 days after the booster immunization of inactivated COVID-19 vaccine.	14 days after the booster immunization of inactivated COVID-19 vaccine
Secondary	Seropositive rate of neutralizing antibody against SARS-CoV-2 strains	The seropositive rate of neutralizing antibody against SARS-CoV-2 strains at 14 days after the booster immunization of inactivated COVID-19 vaccine.	14 days after the booster immunization of inactivated COVID-19 vaccine
Secondary	GMI of neutralizing antibody against SARS-CoV-2 strains	The GMI of neutralizing antibody against SARS-CoV-2 strains at 14 days after the booster immunization of inactivated COVID-19 vaccine.	14 days after the booster immunization of inactivated COVID-19 vaccine
Secondary	GMT of neutralizing antibody against SARS-CoV-2 strains	The GMT of neutralizing antibody against SARS-CoV-2 strains at 14 days after the booster immunization of inactivated COVID-19 vaccine.	14 days after the booster immunization of inactivated COVID-19 vaccine
Secondary	Seropositive rate of antibody against hepatitis A	Seropositive rate of antibody against hepatitis A 6-8 months after vaccination of Hepatitis A vaccine.	6-8 months after vaccination of Hepatitis A vaccine
Secondary	GMC of antibody against hepatitis A	GMC of antibody against hepatitis A 6-8 months after vaccination of Hepatitis A vaccine.	6-8 months after vaccination of Hepatitis A vaccine
Secondary	Incidence rate of adverse reactions	Incidence rate of adverse reactions within 0-28 days after booster immunization with COVID-19 vaccine.	0-28 days after booster immunization with COVID-19 vaccine.