Status unknownNCT04659239Updated Feb 10, 2021

The Efficacy, Safety and Immunogenicity Study of Inactivated SARS-CoV-2 Vaccine for Preventing Against COVID-19

A Phase 3 interventional study of Inactivated SARS-CoV-2 Vaccine (Vero cell) and Placebo in COVID-19, sponsored by Chinese Academy of Medical Sciences. Status unknown at 2 sites in 2 countries. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2021-02-10.

Sponsored by Chinese Academy of Medical Sciences · Phase 3, Interventional, and Prevention

The sponsor has not verified this record recently (last verified Feb 2021), so the status shown — last known as Enrolling by invitation — may be out of date.

Phase: Phase 3
Study type: Interventional
Enrollment: 34,020
Allocation: Randomized
Ages: 18 Years and older
Sex: All

Study summary

This is a randomized, double-blinded, placebo controlled phase III clinical trial to evaluate the efficacy, safety and immunogenicity of SARS-CoV-2 Vaccine, Inactivated (Vero Cell) in adults aged 18 years and above after 2-dose schedule.

Read the detailed description

The trial includes two parts, namely the efficacy study and immunogenicity bridging study. A total of 34020 participants will be enrolled, i.e. 32820 for efficacy cohort, and 1200 for domestic immunogenicity cohort in China.

Efficacy study: Participants will be randomly inoculated with two doses of investigational vaccine or placebo according to 1:1 ratio following Day 0-Day 14 immunization schedule and will be observed from the first dose of investigational vaccine to collect symptomatic and laboratory-confirmed COVID-19 cases for the evaluation of the efficacy of the investigational vaccine.

Immunogenicity bridging study: Before inoculating the first dose, 14 days, 6 months and 12 months after the whole-course immunization, blood samples will be taken for determination of neutralizing antibody and IgG antibody against SARS-CoV-2 (ELISA method); and before inoculating the first dose, 6 months and 12 months after the whole-course immunization, blood samples will be taken for detecting specific T cells with the ELISPOT assay with an aim to evaluate immunogenicity and immune persistence.

Safety observations for all participants will be conducted from the first dose to 28 days after the whole-course immunization, and follow-up of SAEs will also be conducted from the first dose to at least 12 months after the whole-course immunization to evaluate the safety of the investigational vaccine.

Conditions studied

COVID-19

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In context

COVID-19

7,640 studies on the registry are indexed under COVID-19; 488 are open to participants now.

This study's planned enrollment of 34,020 is above the median of 100 across 4,099 interventional studies indexed under COVID-19.

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Lead sponsor

Chinese Academy of Medical Sciences is the lead sponsor of 235 studies on the registry; 19 are open to participants now.

Counted across the registry records on this site, refreshed daily.

Who can participate

Ages eligible: 18 Years and older
Sexes eligible: All
Accepts healthy volunteers: Yes

Inclusion criteria

Adults aged 18 years and above (including boundary values), both female and male.
Legal identification of the participants shall be provided.
Participants shall understand the content in the Informed Consent Form (ICF) and the vaccine for administration, sign the ICF voluntarily and are capable of using thermometers and rulers, and filling in diary cards and contact cards as per the requirements.
Subject shall be able to communicate well with investigators, understand and comply with the requirements of this study.
Participants with oral temperature ≤ 37.9 ℃.
Female participants of childbearing potential (defined as any female who has experienced menarche and who is NOT surgically sterile [i.e., hysterectomy, bilateral tubal ligation, or bilateral oophorectomy] or postmenopausal [defined as amenorrhea at least 12 consecutive months]) must agree to be heterosexually inactive OR consistently use any of the following methods of contraception:
1. Condoms (male or female)
2. Diaphragm with spermicide
3. Cervical cap with spermicide
4. Intrauterine device
5. Oral or patch contraceptives
6. Any country regulatory-approved contraceptive method that is designed to protect against pregnancy
7. Abstinence, as a form of contraception, is acceptable if in line with the participant's lifestyle (other approaches to abstinence are not acceptable).

Exclusion criteria

Exclusion Criteria:

Contraindications to commonly used vaccines;
History of allergy to any vaccines or drug;
Received any vaccine within 1 month before the first dose of vaccination；
Serious diseases required to be excluded, including but not limited to history of diseases in nervous system, cardiovascular system, blood and lymphatic system, immune system, kidney, liver, gastrointestinal tract, respiratory system, metabolism, bones and other systems, and a history of malignant tumors;
Before immunizing the first dose of investigational vaccine, those who developed acute disease within 2 weeks, or had symptoms of fever or upper respiratory tract infection within 7 days;
Those who have a hereditary bleeding tendency or blood coagulation dysfunction, or a history of thrombosis or hemorrhagic disease；
Surgical removal of whole or part of spleen for any reason；
Those who have undergone surgery within 3 months before signing the ICF or those who plan to undergo surgery during or within 3 months after completion of the trial (including plastic surgery, dental and oral surgery);
Those who donated or lost blood (≥400 mL) in the past 3 months, who received blood transfusion or use of blood products, or who plan blood donation during the trial;
Those who received other investigational or unregistered products (drugs, vaccines, biological product or devices) in the past 3 months before signing the ICF, or plan to use them during the study.
Those who received immunosuppressant therapy within 6 months before signing the ICF, such as long-term systemic glucocorticoid treatment (with systemic glucocorticoid therapy for more than 2 consecutive weeks within 6 months, such as prednisone or similar drugs), but local administration is permitted (such as ointment, eye drops, inhalants, or nasal spray). The local administration should not exceed the recommended dose in the package insert or have any signs of systemic exposure;
Participants cannot meet the criteria through the comprehensive physical examination, mainly including:
- Abnormal vital signs with clinical significance (awakening heart rate \<55 beats/min or >100 beats/min, systolic blood pressure ≥140mmHg or diastolic blood pressure ≥90mmHg);
- Those who tested positive for type 1 or type 2 human immunodeficiency virus (HIV-1/2) antibody, or SARS-CoV-2 nucleic acid;
History of COVID-19;
Participants who have a positive pregnancy test, or are breastfeeding, or planning pregnancy, or plan to donate sperm or eggs within 12 months from the screening period to the whole-course immunization;
Participants who are considered as inappropriate for the trial by investigators.
Suspected or known current alcohol or drug dependency.
Investigator site personnel directly related to this study and/or their immediate families; immediate family is defined as a spouse, parent, child, or sibling, whether biological or legally adopted.

Study design

Phase: Phase 3
Primary purpose: Prevention
Allocation: Randomized
Intervention model: Parallel assignment
Masking: Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment: 34,020 participants (estimated)

Study arms

Experimental
Investigational Vaccine
Participants will receive 2 doses of the inactivated SARS-CoV-2 vaccine (Vero cell) according to the immunization schedule of D0, D14.
Biological: Inactivated SARS-CoV-2 Vaccine (Vero cell)
Placebo comparator
Placebo
Participants will receive 2 doses of the placebo according to the immunization schedule of D0, D14.
Biological: Placebo

Interventions

BiologicalInactivated SARS-CoV-2 Vaccine (Vero cell)
The inactivated SARS-CoV-2 vaccine (vero cell) was manufactured by IMBCAMS. Each dose of 0.5ml is for per person per time use.
BiologicalPlacebo
The placebo was manufactured by IMBCAMS. Each dose of 0.5ml is for per person per time use.

What researchers measure

Primary outcomes

The incidence of COVID-19 cases after two-doses of vaccination
The incidence of the symptomatic and laboratory-confirmed COVID-19 cases starting from Day 14 after the second dose.
Time frame: From 14 days after the second dose to 1 year after the second dose.
The incidence of solicited AEs.
The incidence of solicited AEs at the inoculation site (local) and solicited AEs at the non-inoculation site (systemic) within 7 days after each dose
Time frame: 7 days after each dose

Secondary outcomes

The incidence of COVID-19 cases after at least one dose of immunization.
The incidence of the symptomatic and laboratory-confirmed COVID-19 cases after at least one dose of immunization.
Time frame: From the first dose to 1 year after the second dose.
The Geometric Mean Titer (GMT) of neutralizing antibody
The Geometric Mean Titer (GMT) of neutralizing antibody against SARS-CoV-2 14 days after the whole-course immunization.
Time frame: 14 days after the whole-course immunization
The Geometric Mean Titer (GMT) of IgG antibody
The Geometric Mean Titer (GMT) of IgG antibody (ELISA method) against SARS-CoV-2 14 days after the whole-course immunization.
Time frame: 14 days after the whole-course immunization
The positive rates of neutralizing antibody
The positive rates of neutralizing antibody against SARS-CoV-2 14 days after the whole-course immunization.
Time frame: 14 days after the whole-course immunization
The positive rates of IgG antibody
The positive rates of IgG antibody (ELISA method) against SARS-CoV-2 14 days after the whole-course immunization.
Time frame: 14 days after the whole-course immunization
The seroconversion rates of neutralizing antibody
The seroconversion rates of neutralizing antibody against SARS-CoV-2 14 days after the whole-course immunization.
Time frame: 14 days after the whole-course immunization
The seroconversion rates of IgG antibody
The seroconversion rates of IgG antibody (ELISA method) against SARS-CoV-2 14 days after the whole-course immunization.
Time frame: 14 days after the whole-course immunization
The positive rates of neutralizing antibody
The positive rates of neutralizing antibody against SARS-CoV-2 6 months and 12 months after whole-course immunization.
Time frame: 6 months and 12 months after whole-course immunization.
The positive rates of IgG antibody
The positive rates of IgG antibody (ELISA method) against SARS-CoV-2 6 months and 12 months after whole-course immunization.
Time frame: 6 months and 12 months after whole-course immunization.
The Geometric Mean Titer (GMT) of neutralizing antibody
The Geometric Mean Titer (GMT) of neutralizing antibody against SARS-CoV-2 6 months and 12 months after whole-course immunization.
Time frame: 6 months and 12 months after whole-course immunization.
The Geometric Mean Titer (GMT) of IgG antibody
The Geometric Mean Titer (GMT) of IgG antibody (ELISA method) against SARS-CoV-2 6 months and 12 months after whole-course immunization.
Time frame: 6 months and 12 months after whole-course immunization.
Specific T cells with ELISPOT assay
Detecting specific T cells with ELISPOT assay 6 months and 12 months after the whole-course immunization
Time frame: 6 months and 12 months after the whole-course immunization
The incidence of AEs
The incidence of AEs from the first dose to 28 days after whole-course immunization
Time frame: From the first dose to 28 days after whole-course immunization.
The incidence of SAEs
The incidence of SAEs from the first dose to at least 12 months after whole-course immunization.
Time frame: From the first dose to at least 12 months after whole-course immunization.
The occurrence of Antibody Dependent Enhancement (ADE)/ Vaccine Enhanced Disease(VED)
The occurrence of Antibody Dependent Enhancement (ADE)/ Vaccine Enhanced Disease(VED) that probably related to the laboratory-confirmed COVID-19 from 14 days after the second dose till the end of trial.
Time frame: From 14 days after the second dose to 1 year after the second dose.

Other outcomes

The surrogate endpoint of immunogenicity
The correlation between the efficacy of the vaccine and the levels of neutralizing antibody and IgG antibody against SARS-CoV-2.
Time frame: From 14 days after the second dose to 1 year after the second dose.

Study locations

2 sites

CEMEC Pesquisa Clinica
São Bernardo do Campo, São Paulo, Brazil
Hospital Sungai Buloh
Sungai Buloh, Selangor 47000, Malaysia

Updates

Tracking since Sep 25, 2026

No changes since tracking began. The registry record was last updated on Feb 10, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗

Registry details

Key details

Study ID: NCT04659239
Lead sponsor: Chinese Academy of Medical Sciences
Responsible party: Qihan Li (Professor, Chinese Academy of Medical Sciences) — Principal investigator
First posted: Dec 9, 2020
Start date: Jan 28, 2021
Primary completion: Sep 2021 (estimated)
Completion: Jul 2022 (estimated)
Last update: Feb 10, 2021

Study contacts

Yasmin binti Mohamed Gani, PhD

principal investigator · Hospital Sungai Buloh

Adilson JW Cavalcante, PhD

principal investigator · CEMEC Pesquisa Clinica

Oversight

Data monitoring committee: Yes
FDA-regulated drug: No
FDA-regulated device: No

View the source record on ClinicalTrials.gov ↗

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