A Clinical Trial on Booster Immunization of Two COVID-19 Vaccines Constructed From Different Technical Routes
NCT05886790 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 450
Last updated 2023-06-02
Summary
This is an open-label, randomized, parallel-controlled clinical trial conducted in people aged 18 years and older to evaluate the immunogenicity and safety of two SARS-CoV-2 bivalent vaccines constructed by adenovirus type 5-based or mRNA-based technics.
Conditions
Interventions
- BIOLOGICAL
-
Prototype and Omicron BA.4/5 Bivalent Recombinant COVID-19 Vaccine(Adenovirus Type 5 Vector) For Inhalation
Containing two adenovirus type 5-based vaccines delivering the spike proteins of SARS-CoV-2 wild type and Omicron BA.4/5 mutant, respectively
- BIOLOGICAL
-
Bivalent COVID-19 mRNA Vaccine
Containing two mRNA-based vaccines delivering the spike proteins of SARS-CoV-2 Beta and Omicron BA.4/5 mutant, respectively
- BIOLOGICAL
-
Recombinant COVID-19 Vaccine (Adenovirus Type 5 Vector) For Inhalation
Containing adenovirus type 5-based vaccine delivering the spike proteins of SARS-CoV-2 wild type
Sponsors & Collaborators
-
Institute of Biotechnology, Academy of Military Medical Sciences, PLA of China
collaborator OTHER -
Zhongnan Hospital
lead OTHER
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2023-05-30
- Primary Completion
- 2023-12-31
- Completion
- 2024-05-29
Countries
- China
Study Locations
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