A Study to Evaluate The Efficacy, Safety and Immunogenicity of Inactivated SARS-CoV-2 Vaccines (Vero Cell) in Healthy Population Aged 18 Years Old and Above

COVID-19 Clinical Trial

— COVID-19  

Official title:

Multicenter, Randomized, Double Blind, Parallel Placebo Controlled, Phase III Clinical Trial to Evaluate the Protective Efficacy, Safety and Immunogenicity of Inactivated SARS-CoV-2 Vaccines (Vero Cell) in Healthy Population Aged 18 Years Old and Above

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04510207
• Other study ID #: CNBG2020003SQ
• Status: Completed
• Phase: Phase 3
• Start date: July 16, 2020
• Est. completion date: December 31, 2021

Study information

• Verified date: June 2023
• Source: China National Biotec Group Company Limited
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a multicenter, randomized, double blind, parallel placebo controlled, phase 3 clinical trial to evaluate the protective efficacy, safety and immunogenicity of inactivated SARS-CoV-2 vaccines in healthy population 18 years old and above.

Description:

This is a multicenter, randomized, double-blind, placebo-controlled study to evaluate the protective efficacy, safety and immunogenicity of inactivated SARS-CoV-2 vaccines in healthy population 18 years old and above. The participants were randomized into three groups of investigational vaccine 1, investigational vaccine 2 and placebo in a 1:1:1 ratio.2 doses of the investigational vaccine or placebo are inoculated into the deltoid muscle of the either arm according to the vaccination schedule of D0 & D21 (+7 days).According to the immune durability results in Phase I/II study, and cross-neutralization assay results, a third dose (booster dose) generates a better immune response and is estimated to offer better protection, therefore, a booster dose will be given after 3 months

Recruitment information / eligibility

• Status: Completed
• Enrollment: 44101
• Est. completion date: December 31, 2021
• Est. primary completion date: June 16, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Healthy subjects aged 18 years old and above.

2. By asking for medical history and physical examination, the investigator judged that the health condition is well.

3. Female subjects of childbearing age are not nursing or pregnant at the time of enrolment (negative urine pregnancy test) and have no family planning within the first 3 months after enrolment. Effective contraceptive measures have been taken within 2 weeks before inclusion.

4. During the whole follow-up period of the study, be able and willing to complete the whole prescribed study plan.

5. With self-ability to understand the study procedures, the informed consent & voluntarily sign an informed consent form and be able to comply with the requirements of the clinical study protocol.

Exclusion Criteria:

1. Confirmed acute cases of SARS-CoV-2 Infection.

2. Have a history of SARS, MERS infection (self-report, on-site inquiry).

3. Positive urine pregnancy test result.

4. Fever (body temperature > 37.0 ?), dry cough, fatigue, nasal obstruction, runny nose, pharyngeal pain, myalgia, diarrhea, shortness of breath and dyspnea occurred within 14 days before vaccination.

5. Axillary body temperature > 37.0 ? before vaccination.

6. Previous severe allergic reactions to vaccination (such as acute allergic reactions, urticaria, dyspnea, angioneurotic edema or abdominal pain) or allergy to known ingredients of inactivated SARS-CoV-2 vaccine have occurred.

7. Has a history of convulsion, epilepsy, encephalopathy or mental illness or family history.

8. With congenital malformations or developmental disorders, genetic defects, severe malnutrition, etc.

9. With severe liver diseases, severe kidney diseases defined as eGFR less than 60, uncontrollable hypertension (systolic blood pressure >150 mmHg, diastolic blood pressure > 90 mmHg), diabetic complications, malignant tumors, various acute diseases, or acute attack period of chronic diseases.

10. Has been diagnosed with congenital or acquired immune deficiency, HIV infection, lymphoma, leukemia or other autoimmune diseases.

11. With known or suspected diseases include acute respiratory diseases (e.g. influenza like illness, acute cough, sore throat), severe cardiovascular diseases, liver and kidney diseases, and malignant tumors.

12. Has a history of coagulation dysfunction (e.g. Coagulation factor deficiency, coagulation disease).

13. Receiving anti-TB therapy.

14. Patients receiving immunotherapy or inhibitor therapy within 3 months (continuous oral or infusion for more than 14 days).

15. Live attenuated vaccine is inoculated within 1 month before this vaccination, other vaccines are inoculated within 14 days before this vaccination.

16. Received blood products within 3 months before this vaccination

17. Received other research drugs within 6 months before this vaccination.

18. Other circumstances judged by investigators that are not suitable for this clinical trial.

Related Conditions & MeSH terms

• COVID-19

Intervention

Biological:
• Inactivated SARS-CoV-2 Vaccine (Vero cell)
The inactivated SARS-CoV-2 Vaccine (Vero cell) manufactured by WIBP
• Inactivated SARS-CoV-2 Vaccine (Vero cell)
The inactivated SARS-CoV-2 Vaccine (Vero cell) manufactured by BIBP
• Placebo
The placebo of inactivated SARS-CoV-2 Vaccine (Vero cell) manufactured by WIBP

Locations

Country	Name	City	State
Bahrain	Bahrain International Exhibition & Convention Centre Affiliated to Salymynia Medical Complex S	Sanabis
Egypt	Katameya Medical Center	Cairo
Egypt	Vacsera health Care facilities , MoH	Cairo
Jordan	Prince Hamza Hospital	Amman
United Arab Emirates	Sheikh Khalifa Medical City, SEHA	Abu Dhabi
United Arab Emirates	Al Qarain Primary Health Care Centre-MOHAP	Sharjah

Sponsors (5)

Lead Sponsor	Collaborator
China National Biotec Group Company Limited	Abu Dhabi Health Services Company, Beijing Institute of Biological Products Co Ltd., G42 Healthcare company, Wuhan Institute of Biological Products Co., Ltd

Countries where clinical trial is conducted

Bahrain,  Egypt,  Jordan,  United Arab Emirates, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	the anti-SARS-CoV-2 neutralizing antibody protective level against COVID-19		14 days after 2 doses of vaccination
Other	The occurrence of ADE		From the beginning of the first dose to 12 months after the second immunization
Primary	The incidence of COVID-19 cases after two-doses of vaccination		From14 days after the second dose to 6 month after the second dose
Primary	The incidence of COVID-19 cases after the booster dose of immunization		From 14 days after the booster dose
Secondary	The incidence of severe cases of COVID-19 and deaths accompanied by COVID-19 after two-doses of vaccination		From 14 day after the second dose to 6 month after the second dose
Secondary	The incidence of severe cases of COVID-19 and deaths accompanied by COVID-19 after two-doses of vaccination		From 14 day after the booster dose
Secondary	The incidence of any adverse reactions/events		28 days after each immunization
Secondary	The incidence of serious adverse events (SAE)		From the beginning of the first dose to 12 months after the second immunization
Secondary	The Geometric Mean Titer (GMT) of anti-SARS-CoV-2 neutralizing antibody		14 days after full course of immunization
Secondary	The four-fold increase rate of anti-SARS-CoV-2 neutralizing antibody		14 days after full course of immunization
Secondary	The Geometric Mean Fold Rise (GMFR) of anti-SARS-CoV-2 neutralizing antibody		14 days after full course of immunization
Secondary	The Geometric Mean Titer (GMT) of anti-SARS-CoV-2 neutralizing antibody		28 days, 3rd month, 6th month, 9th month, and 12th month after 2 doses of immunization
Secondary	The 4-fold increase rate of anti-SARS-CoV-2 neutralizing antibody		28 days, 3rd month, 6th month, 9th month, and 12th month after 2 doses of immunization
Secondary	The Geometric Mean Fold Rise (GMFR) of anti-SARS-CoV-2 neutralizing antibody		28 days, 3rd month, 6th month, 9th month, and 12th month after 2 doses of immunization
Secondary	The Geometric Mean Titer (GMT) of anti-SARS-CoV-2 neutralizing antibody		14 days, 28 days and 6th month after the booster dose
Secondary	The 4-fold increase rate of anti-SARS-CoV-2 neutralizing antibody		14 days, 28 days and 6th month after the booster dose
Secondary	The Geometric Mean Fold Rise (GMFR) of anti-SARS-CoV-2 neutralizing antibody		14 days, 28 days and 6th month after the booster dose