Clinical Trial of SARS-CoV-2 mRNA Vaccine in China
NCT05364047 · Status: UNKNOWN · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 144
Last updated 2022-12-05
Summary
This study is a phase I clinical trial. The investigators intent to evaluate the safety, tolerability and preliminary immunogenicity of SARS-CoV-2 mRNA vaccine (LVRNA009) in Chinese people aged 18 years and over.
Conditions
Interventions
- BIOLOGICAL
-
Low-dose of LVRNA009
25μg/person
- BIOLOGICAL
-
Middle-dose of LVRNA009
50μg/person
- BIOLOGICAL
-
High-dose of LVRNA009
100μg/person
- OTHER
-
Placebo
0.5ml/person
Sponsors & Collaborators
-
Shulan (Hangzhou) Hospital
collaborator OTHER -
Yuncheng Central Hospital
collaborator OTHER -
AIM Vaccine Co., Ltd.
lead INDUSTRY
Principal Investigators
-
Lanjuan Li · Shulan (Hangzhou) Hospital
-
Guiling Chen · Shulan (Hangzhou) Hospital
-
Fengli Zhao · Yuncheng Central Hospital
-
Jinlian Bi · Xiangya Boai Rehabilitation Hospital
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2021-07-31
- Primary Completion
- 2022-10-14
- Completion
- 2023-10-31
Countries
- China
Study Locations
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