Study on Sequential Immunization of Omicron Inactivated COVID-19 Vaccine and Prototype Inactivated COVID-19 Vaccine in Population Aged 18 Years Old and Above

Sponsor
China National Biotec Group Company Limited (Industry)
Overall Status
Recruiting
CT.gov ID
NCT05374954
Collaborator
Beijing Institute of Biological Products Co Ltd. (Industry), Hunan Provincial Center for Disease Control and Prevention (Other)
4,200
3
28
18
1400
77.6

Study Details

Study Description

Brief Summary

This is a randomized, double blind, positive controlled study to evaluate the safety and immunogenicity of Omicron COVID-19 Vaccine (Vero Cell), Inactivated in population aged 18 years old and above who have been vaccinated with 2 or 3 doses of COVID-19 Vaccine (Vero Cell), Inactivated manufactured by Beijing Institute of Biological Products, Co., Ltd.

Condition or Disease Intervention/Treatment Phase
  • Biological: Omicron COVID-19 Vaccine (Vero Cell), Inactivated
  • Biological: COVID-19 Vaccine (Vero Cell), Inactivated
Phase 3

Detailed Description

This is a randomized, double blind, positive controlled study to evaluate the safety and immunogenicity of Omicron COVID-19 Vaccine (Vero Cell), Inactivated in population aged 18 years old and above who have been vaccinated with 2 or 3 doses of COVID-19 Vaccine (Vero Cell), Inactivated manufactured by Beijing Institute of Biological Products, Co., Ltd. According to subject's age (18-59 vs 60 and above), doses of vaccination history ( 2 doses vs 3 doses), and vaccination interval, the subjects will be stratified and assigned randomly to the study groups ( Omicron inactivated COVID-19 Vaccine) or the control groups ( Prototype inactivated COVID-19 Vaccine) in a 2:1 ratio. All subjects will receive single dose or two doses of vaccine with a interval of 28 days. The occurrence of adverse events within 28 days and serious adverse events within 12 months after vaccination will be observed. The serum antibody levels, cellular immune responses will be analyzed at different time points.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
4200 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Safety and Immunogenicity Study on Omicron Inactivated COVID-19 Vaccine and Prototype Inactivated COVID-19 Vaccine in Population Aged 18 Years Old and Above Vaccinated the Prototype Inactivated COVID-19 Vaccine
Actual Study Start Date :
May 10, 2022
Anticipated Primary Completion Date :
Oct 10, 2022
Anticipated Study Completion Date :
Nov 10, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: A1:one dose, 18-59 years old, from 3 months to 6 months after 2 doses of vaccination

subjects aged 18-59 years old will be blinded and receive one dose from 3 months to 6 months after 2 doses of inactivated COVID-19 vaccine

Biological: Omicron COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Active Comparator: A2:one dose, 18-59 years old, from 3 months to 6 months after 2 doses of vaccination

subjects aged 18-59 years old will be blinded and receive one dose from 3 months to 6 months after 2 doses of inactivated COVID-19 vaccine

Biological: COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Experimental: A3:one dose, 18-59 years old, from 6 months to 12 months after 2 doses of vaccination

subjects aged 18-59 years old will be blinded and receive one dose from 6 months to 12 months after 2 doses of inactivated COVID-19 vaccine

Biological: Omicron COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Active Comparator: A4:one dose, 18-59 years old, from 6 months to 12 months after 2 doses of vaccination

subjects aged 18-59 years old will be blinded and receive one dose from 6 months to 12 months after 2 doses of inactivated COVID-19 vaccine

Biological: COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Experimental: B1:one dose, 18-59 years old, from 3 months to 6 months after 3 doses of vaccination

subjects aged 18-59 years old will be blinded and receive one dose from 3 months to 6 months after 3 doses of inactivated COVID-19 vaccine

Biological: Omicron COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Active Comparator: B2:one dose, 18-59 years old, from 3 months to 6 months after 3 doses of vaccination

subjects aged 18-59 years old will be blinded and receive one dose from 3 months to 6 months after 3 doses of inactivated COVID-19 vaccine

Biological: COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Experimental: B3:one dose, 18-59 years old, from 6 months to 12 months after 3 doses of vaccination

subjects aged 18-59 years old will be blinded and receive one dose from 6 months to 12 months after 3 doses of inactivated COVID-19 vaccine

Biological: Omicron COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Active Comparator: B4:one dose, 18-59 years old, from 6 months to 12 months after 3 doses of vaccination

subjects aged 18-59 years old will be blinded and receive one dose from 6 months to 12 months after 3 doses of inactivated COVID-19 vaccine

Biological: COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Experimental: C1:two doses, 18-59 years old, from 3 months to 6 months after 2 doses of vaccination

subjects aged 18-59 years old will be blinded and receive two doses of vaccine with 28 days apart from 3 months to 6 months after 2 doses of inactivated COVID-19 vaccine

Biological: Omicron COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Active Comparator: C2:two doses, 18-59 years old, from 3 months to 6 months after 2 doses of vaccination

subjects aged 18-59 years old will be blinded and receive two doses of vaccine with 28 days apart from 3 months to 6 months after 2 doses of inactivated COVID-19 vaccine

Biological: COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Experimental: C3:two doses, 18-59 years old, from 6 months to 12 months after 2 doses of vaccination

subjects aged 18-59 years old will be blinded and receive two doses of vaccine with 28 days apart from 6 months to 12 months after 2 doses of inactivated COVID-19 vaccine

Biological: Omicron COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Active Comparator: C4:two doses, 18-59 years old, from 6 months to 12 months after 2 doses of vaccination

subjects aged 18-59 years old will be blinded and receive two doses of vaccine with 28 days apart from 6 months to 12 months after 2 doses of inactivated COVID-19 vaccine

Biological: COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Experimental: C5:two doses, 18-59 years old, more than 12 months after 2 doses of vaccination

subjects aged 18-59 years old will be blinded and receive two doses of vaccine with 28 days apart more than 12 months after 2 doses of inactivated COVID-19 vaccine

Biological: Omicron COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Active Comparator: C6:two doses, 18-59 years old, more than 12 months after 2 doses of vaccination

subjects aged 18-59 years old will be blinded and receive two doses of vaccine with 28 days apart more than 12 months after 2 doses of inactivated COVID-19 vaccine

Biological: COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Experimental: D1:two doses, 60 years old and above, from 3 months to 6 months after 2 doses of vaccination

subjects aged 60 years old and above will be blinded and receive two doses of vaccine with 28 days apart from 3 months to 6 months after 2 doses of inactivated COVID-19 vaccine

Biological: Omicron COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Active Comparator: D2:two doses, 60 years old and above, from 3 months to 6 months after 2 doses of vaccination

subjects aged 60 years old and above will be blinded and receive two doses of vaccine with 28 days apart from 3 months to 6 months after 2 doses of inactivated COVID-19 vaccine

Biological: COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Experimental: D3:two doses, 60 years old and above, from 6 months to 12 months after 2 doses of vaccination

subjects aged 60 years old and above will be blinded and receive two doses of vaccine with 28 days apart from 6 months to 12 months after 2 doses of inactivated COVID-19 vaccine

Biological: Omicron COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Active Comparator: D4:two doses, 60 years old and above, from 6 months to 12 months after 2 doses of vaccination

subjects aged 60 years old and above will be blinded and receive two doses of vaccine with 28 days apart from 6 months to 12 months after 2 doses of inactivated COVID-19 vaccine

Biological: COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Experimental: E1:two doses, 18-59 years old, from 3 months to 6 months after 3 doses of vaccination

subjects aged 18-59 years old will be blinded and receive two doses of vaccine with 28 days apart from 3 months to 6 months after 3 doses of inactivated COVID-19 vaccine

Biological: Omicron COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Active Comparator: E2:two doses, 18-59 years old, from 3 months to 6 months after 3 doses of vaccination

subjects aged 18-59 years old will be blinded and receive two doses of vaccine with 28 days apart from 3 months to 6 months after 3 doses of inactivated COVID-19 vaccine

Biological: COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Experimental: E3:two doses, 18-59 years old, from 6 months to 12 months after 3 doses of vaccination

subjects aged 18-59 years old will be blinded and receive two doses of vaccine with 28 days apart from 6 months to 12 months after 3 doses of inactivated COVID-19 vaccine

Biological: Omicron COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Active Comparator: E4:two doses, 18-59 years old, from 6 months to 12 months after 3 doses of vaccination

subjects aged 18-59 years old will be blinded and receive two doses of vaccine with 28 days apart from 6 months to 12 months after 3 doses of inactivated COVID-19 vaccine

Biological: COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Experimental: E5:two doses, 18-59 years old, more than 12 months after 3 doses of vaccination

subjects aged 18-59 years old will be blinded and receive two doses of vaccine with 28 days apart more than 12 months after 3 doses of inactivated COVID-19 vaccine

Biological: Omicron COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Active Comparator: E6:two doses, 18-59 years old, more than 12 months after 3 doses of vaccination

subjects aged 18-59 years old will be blinded and receive two doses of vaccine with 28 days apart more than 12 months after 3 doses of inactivated COVID-19 vaccine

Biological: COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Experimental: F1:two doses, 60 years old and above, from 3 months to 6 months after 3 doses of vaccination

subjects aged 60 years old and above will be blinded and receive two doses of vaccine with 28 days apart from 3 months to 6 months after 3 doses of inactivated COVID-19 vaccine

Biological: Omicron COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Active Comparator: F2:two doses, 60 years old and above, from 3 months to 6 months after 3 doses of vaccination

subjects aged 60 years old and above will be blinded and receive two doses of vaccine with 28 days apart from 3 months to 6 months after 3 doses of inactivated COVID-19 vaccine

Biological: COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Experimental: F3:two doses, 60 years old and above, from 6 months to 12 months after 3 doses of vaccination

subjects aged 60 years old and above will be blinded and receive two doses of vaccine with 28 days apart from 6 months to 12 months after 3 doses of inactivated COVID-19 vaccine

Biological: Omicron COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Active Comparator: F4:two doses, 60 years old and above, from 6 months to 12 months after 3 doses of vaccination

subjects aged 60 years old and above will be blinded and receive two doses of vaccine with 28 days apart from 6 months to 12 months after 3 doses of inactivated COVID-19 vaccine

Biological: COVID-19 Vaccine (Vero Cell), Inactivated
intramuscular injection in the deltoid muscle

Outcome Measures

Primary Outcome Measures

  1. The Geometric Mean Titer (GMT) of neutralizing antibody against Omicron SARS-CoV-2 [On Day 28 after vaccination]

  2. The four-fold increase rate of neutralizing antibody against Omicron SARS-CoV-2 [On Day 28 after vaccination]

  3. Incidence of adverse reactions [within 28 days after vaccination]

Secondary Outcome Measures

  1. The GMT of neutralizing antibody against Omicron SARS-CoV-2 [On Day 14 after vaccination]

  2. The four-fold increase rate of neutralizing antibody against Omicron SARS-CoV-2 [On Day 14 after vaccination]

  3. Specific cellular immune response [within 28 days after vaccination]

  4. The neutralizing antibody GMT [on 3rd month, 6th month, 9th month, and 12th month after vaccination]

  5. The proportion of subjects with neutralizing antibody GMT ≥1:16,≥1:32 and ≥1:64 [on 3rd month, 6th month, 9th month, and 12th month after vaccination]

  6. The incidence of any adverse reactions/events [28 days after each immunization]

  7. The incidence of serious adverse events (SAE) and adverse events special interest (AESI) [From the beginning of the first dose to 12 months after vaccination]

Other Outcome Measures

  1. The neutralizing antibody GMT to different variants of SARS-CoV-2 [On Day 28 after vaccination]

  2. The IgG antibody lever against Omicron SARS-CoV-2 [On Day 14 and Day 28 after vaccination]

  3. The incidence of COVID-19 cases , including severe cases and deaths accompanied by COVID-19 [From 14 day after vaccination]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Healthy subjects aged 18 years old and above.

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

  • Has been vaccinated 2 or 3 doses of inactivated COVID-19 vaccine manufactured by BIBP more than 3 months.

  • 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 12 months after enrolment. Effective contraceptive measures have been taken within 2 weeks before inclusion.

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

  • 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:
  • Confirmed or suspected cases of SARS-CoV-2 Infection.

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

  • Received one dose or more than 3 doses of inactivated COVID-19 vaccine manufactured by BIBP

  • Received COVID-19 vaccine manufactured bu other companies (include mRNA, recombinant protein vaccines, vector vaccines, inactivated vaccines, etc.)

  • Axillary body temperature > 37.3 ℃ before vaccination

  • 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 (self-report, on-site inquiry).

  • History of hospital-diagnosed thrombocytopenia or other coagulation disorder

  • Known immunological impairment or low level with hospital diagnosis

  • History of uncontrolled epilepsy, other progressive neurological disorders, or Guillain-Barre syndrome (self-report, on-site inquiry).

  • Known or suspected concomitant serious diseases include: respiratory disease, acute infection or active chronic disease, liver and kidney disease, severe diabetes, malignant tumor, infection or allergic skin disease, HIV infection.

  • Severe cardiovascular disease (cardiopulmonary failure, uncontrolled hypertension, etc.) diagnosed by the hospital, active chronic respiratory disease

  • Received live attenuated vaccine within 1 month before enrollment.

  • Received other vaccines within 14 days before enrollment.

  • Be participating in or plan to participate in other vaccine clinical trials during this study.

  • Contraindications related to vaccination as considered by other investigators.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Linli County Center for Disease Control and Prevention Changde Hunan China 415200
2 Changning Center for Disease Control and Prevention Changning Hunan China 421500
3 You County Center for Disease Control and Prevention Zhuzhou Hunan China 412300

Sponsors and Collaborators

  • China National Biotec Group Company Limited
  • Beijing Institute of Biological Products Co Ltd.
  • Hunan Provincial Center for Disease Control and Prevention

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
China National Biotec Group Company Limited
ClinicalTrials.gov Identifier:
NCT05374954
Other Study ID Numbers:
  • CNBG-BIBP-O-2022004
First Posted:
May 16, 2022
Last Update Posted:
Jun 1, 2022
Last Verified:
May 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by China National Biotec Group Company Limited
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 1, 2022