Evaluate the Safety and Immunogenicity of a SARS-CoV-2 mRNA Vaccine Booster
NCT05897190 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 60
Last updated 2024-03-25
Summary
This study is to evaluate the safety and immunogenicity of a SARS-CoV-2 mRNA Vaccine as a heterologous booster dose in adults who completed 2 doses of inactivated vaccination through 12 months in China.
Conditions
Interventions
- BIOLOGICAL
-
SARS-CoV-2 mRNA vaccine (RBMRNA-405)
Dose A
- BIOLOGICAL
-
CoronaVac®
Dose B
Sponsors & Collaborators
-
Argorna Pharmaceuticals Co., LTD
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2022-05-16
- Primary Completion
- 2022-06-13
- Completion
- 2023-05-12
Countries
- China
Study Locations
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