Immunogenicity and Safety of an Inactivated COVID-19 Vaccine

Immunogenicity and Safety of an Inactivated COVID-19 Vaccine for Prevention of COVID-19 in Healthy Population Aged 18 Years and Older

This study is a randomized, placebo-controlled and open design, phase 4 clinical trial of an inactivated COVID-19 vaccine (CoronaVac) manufactured by Sinovac Research and Development Co., Ltd. The purpose of this study is to evaluate the immunogenicity and safety of the CoronaVac in healthy population aged 18 years and older.

Study Overview

• Status: Completed
• Conditions: COVID-19
• Intervention / Treatment: Biological: Inactivated COVID-19 Vaccine; Biological: 23-valent pneumococcal polysaccharide vaccine; Biological: Inactivated Hepatitis A Vaccine

Detailed Description

This study is a randomized, placebo-controlled and opened, phase 4 clinical trial to evaluate the safety and immunogenicity of an inactivated COVID-19 vaccine(CoronaVac）in healthy population aged 18 years and older . The experimental vaccine is manufactured by Sinovac Research and Development Co.,Ltd. A total of 270 healthy subjects will be enrolled, including 135 adults aged 18-59 years and 135 elderly elderly aged 60 years and older. Subjects in each age group will be divided into two groups in a ratio of 1:1. Subjects in the experimental group will receive two doses of CoronaVac on day 0 and day 28. Subjects in the control group will receive one dose of 23-valent Pneumococcal Polysaccharide Vaccine on day 0 and one dose of Inactivated Hepatitis A Vaccine on day 28.

• Study Type: Interventional
• Enrollment (Actual): 270
• Phase: Phase 4

Contacts and Locations

Study Locations

• China
  • Shandong
    • Weihai, Shandong, China, 250014
      • Rushan City Center for Disease Control and Prevention

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Healthy population aged 18 years and above;
• The subjects can understand and voluntarily sign the informed consent form;
• Proven legal identity.

Exclusion Criteria:

• History of SARS-CoV-2 infection;
• Have received any COVID-19 vaccine;
• Participants with abnormal fasting blood glucose or diabetes;
• 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;
• Autoimmune disease or immunodeficiency / immunosuppression;
• Severe chronic diseases, severe cardiovascular diseases, hypertension and diabetes that cannot be controlled by drugs, liver or kidney diseases, malignant tumors, etc.;
• Severe neurological disease (epilepsy, convulsions or convulsions) or mental illness;
• Thyroid disease or history of thyroidectomy, spleenlessness, functional spleenlessness, spleenlessness or splenectomy resulting from any condition;
• Diagnosed abnormal blood coagulation function (eg, lack of blood coagulation factors, blood coagulopathy, abnormal platelets) or obvious bruising or blood coagulation;
• Diseases or factors that are prone to thrombosis or bleeding, such as thrombophlebitis, major surgery/trauma, hereditary thrombotic disorder, sepsis, inflammatory bowel disease, severe varicose veins, May-Thurner syndrome, fibrinolytic activity enhancement disease, history of cardiac stent surgery, allergic purpura, etc.;
• Immunosuppressive therapy, cytotoxic therapy, inhaled corticosteroids (excluding allergic rhinitis corticosteroid spray therapy, acute noncomplicated dermatitis superficial corticosteroid therapy) in the past 6 months;
• Abnormal hematological laboratory test results outside the reference range during previous physical examination within one year: Blood routine indicators (white blood cell count, hemoglobin, platelet count), Coagulation function test (prothrombin time PT, activated partial prothrombin time APTT, fibrinogen FIB, thrombin time TT, international standardized ratio INR, D-dimer), other indicators (blood glucose, platelet factor 4 HIT ELISA, erythrocyte sedimentation rate);
• History of alcohol or drug abuse;
• Receipt of blood products within in the past 3 months;
• Receipt of other investigational drugs in the past 30 days;
• Receipt of attenuated live vaccines in the past 14 days;
• Receipt of inactivated or subunit vaccines in the past 7 days;
• Axillary temperature >37.0°C;
• Already pregnant (including a positive urine pregnancy test) or are breastfeeding, planning to get pregnant within 3 months;
• History of taking aspirin drugs and other drugs that affect blood coagulation;
• According to the investigator's judgment, the subject has any other factors that are not suitable for participating in the clinical trial.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Prevention
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Experimental Group; 180 subjects (including 90 adults aged 18-59 years and 90 elderly aged 60 year and older）will receive two doses of inactivated COVID-19 vaccine on day 0 and day 28	Biological: Inactivated COVID-19 Vaccine; 600SU inactivated virus in 0·5 mL of aluminium hydroxide solution per injection; Other Names: CoronaVac
Placebo Comparator: Control Group; 90 subjects (including 45 adults aged 18-59 years and 45 elderly aged 60 year and older）will receive one dose of 23-valent pneumococcal polysaccharide vaccine on day 0 and one dose of Inactivated Hepatitis A Vaccine on day 28	Biological: 23-valent pneumococcal polysaccharide vaccine; 25μg each of the following serotypes/each dose (0.5ml): 1, 2, 3, 4, 5, 6B, 7F, 8, 9N, 9V, 10A, 11A, 12F, 14, 15B, 17F, 18C, 19A, 19F, 20, 22F, 23F, and 33F; Biological: Inactivated Hepatitis A Vaccine; 500SU inactivated Hepatitis A virus in 1 mL of aluminium hydroxide solution per injection.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Seroconversion rate of the neutralizing antibody to SARS-CoV-2	Seroconversion rate of the neutralizing antibody to SARS-CoV-2 at day 28 after the second dose of inactivated COVID-19 vaccine	Day 28 after the second dose

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Seroconversion rate of the neutralizing antibody to SARS-CoV-2	Seroconversion rate of the neutralizing antibody to SARS-CoV-2 at different points after vaccination	Day 4, 14, 32,42 and 56 after the first dose
Seropositivity rate of the neutralizing antibody to SARS-CoV-2	Seropositivity rate of of the neutralizing antibody to SARS-CoV-2 at different points after vaccination	Day 4, 14, 28, 32,42 and 56 after the first dose
GMT of the neutralizing antibody to SARS-CoV-2	GMT of of the neutralizing antibody to SARS-CoV-2 at different points after vaccination	Day 4, 14, 28, 32,42 and 56 after the first dose
GMI of the neutralizing antibody to SARS-CoV-2	GMT of of the neutralizing antibody to SARS-CoV-2 at different points after vaccination	Day 4, 14, 28, 32,42 and 56 after the first dose
Geometric mean concentrations of anti-pneumococcal antibody for 23 serotypes (ELISA)	Geometric mean concentrations of anti-pneumococcal antibody for 23 serotypes (ELISA) at day 28 after vaccination of 23-valent pneumococcal polysaccharide vaccine	Day 28 after vaccination of 23-valent pneumococcal polysaccharide vaccine
Seroconversion rate of anti-pneumococcal antibody for 23 serotypes (ELISA)	Seroconversion rate of anti-pneumococcal antibody for 23 serotypes (ELISA) at day 28 after vaccination of 23-valent pneumococcal polysaccharide vaccine	Day 28 after vaccination of 23-valent pneumococcal polysaccharide vaccine
Seroconversion rate of the hepatitis A antibody by Electrochemiluminescence	Seroconversion rate of the hepatitis A antibody at day 28 after vaccination of Inactivated Hepatitis A Vaccine	Day 28 after vaccination of Inactivated Hepatitis A Vaccine
Seropositivity rate of the hepatitis A antibody by Electrochemiluminescence	Seropositivity rate of the hepatitis A antibody at day 28 after vaccination of Inactivated Hepatitis A Vaccine	Day 28 after vaccination of Inactivated Hepatitis A Vaccine
GMT of the hepatitis A antibody by Electrochemiluminescence	GMT of the hepatitis A antibody at day 28 after vaccination of Inactivated Hepatitis A Vaccine	Day 28 after vaccination of Inactivated Hepatitis A Vaccine
GMI of the hepatitis A antibody by Electrochemiluminescence	GMI of the hepatitis A antibody at day 28 after vaccination of Inactivated Hepatitis A Vaccine	Day 28 after vaccination of Inactivated Hepatitis A Vaccine
Occurrence of abnormal changes of laboratory safety examinations	Occurrence of abnormal changes of laboratory safety examinations (Platelet factor 4 HIT, blood sugar, ESR, White blood cell count, hemoglobin, platelet count and Coagulation function index)	Day 4, 14, 28, 32,42 and 56 after the first dose

Collaborators and Investigators

• Sponsor: Sinovac Research and Development Co., Ltd.
• Investigators: Principal Investigator: Li Zhang, Master, Shandong Provincial Center for Disease Control and Prevention

Study record dates

Study Major Dates

• Study Start (Actual): July 9, 2021
• Primary Completion (Actual): October 31, 2021
• Study Completion (Actual): January 31, 2022

Study Registration Dates

• First Submitted: July 5, 2021
• First Submitted That Met QC Criteria: July 5, 2021
• First Posted (Actual): July 7, 2021

Study Record Updates

• Last Update Posted (Actual): April 14, 2022
• Last Update Submitted That Met QC Criteria: April 12, 2022
• Last Verified: July 1, 2021

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; Physiological Effects of Drugs; Immunologic Factors; Vaccines; Heptavalent Pneumococcal Conjugate Vaccine
• Other Study ID Numbers: PRO-nCOV-MA4004-SD

Drug and device information, study documents

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