Skip to content

Study on the safety and immunogenicity of the third dose (booster dose) of adenovirus, mRNA, recombinant protein and inactivated vaccine of novel coronavirus in the population that has received two doses of inactivated vaccine

Clinical study to evaluate the safety and immunogenicity of the third dose of adenovirus, mRNA, recombinant protein and inactivated vaccine of novel coronavirus in people who have received two doses of inactivated vaccine (booster shot)

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200057758
Enrollment
Unknown
Registered
2022-03-16
Start date
2022-01-01
Completion date
Unknown
Last updated
2023-11-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Novel Coronavirus Pneumonia (COVID-19)

Interventions

Group 1:Inoculation with adenovirus vaccine
Group 2:Inoculation with mRNA vaccine
Group 3:Inoculation with inactivated vaccine
Group 4:Inoculation with protein subunit vaccine
Group 5:Inoculation with saline solution

Sponsors

The Afiliated Hospital of Yunnan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 59 Years

Inclusion criteria

Inclusion criteria: 1. Subjects aged 18-59 years, no gender limit; 2. Recently received two doses of inactivated COVID-19 vaccine with an interval of 3-5 weeks; 3. Be currently 100-270 days after the second dose of vaccination; 4. Subjects can complete the study process according to the researcher's guidance.

Exclusion criteria

Exclusion criteria: 1. A history of infection with the novel coronavirus; 2. Patients with severe mental and neurological diseases; 3. Patients with the following common diseases (coronary heart disease, hypertension, diabetes, chronic respiratory diseases, tumors, etc.) and poor control; 4. Patients with immune deficiency or immunosuppressive treatment; 5. In the investigator's judgment, the patient has any other ineligible factors for clinical trial participation.

Design outcomes

Primary

MeasureTime frame
Neutralizing antibody titers;Incidence of adverse events;Cellular immune response to SARS-CoV-2;

Secondary

MeasureTime frame
Serious adverse events and adverse event rates of special concern;Titer multiplication rate of neutralizing antibody;Persistence of neutralizing antibody titers;

Countries

China

Contacts

Public ContactWei Jia

The Affiliated Hospital of Yunnan University

weijia19631225@163.com+86 871 65815279

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 13, 2026