Study to Evaluate the Safety of a Lyophilized RSV mRNA Vaccine
NCT07418229 · Status: NOT_YET_RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 60
Last updated 2026-02-18
Summary
To evaluate the safety of Sinovac RSV mRNA among participants aged ≥18 years
Conditions
- RSV
- mRNA Vaccine
Interventions
- BIOLOGICAL
-
Low-dose RSV mRNA vaccine
One dose of RSV mRNA vaccine in low dosage
- BIOLOGICAL
-
High-dose RSV mRNA vaccine
One dose of RSV mRNA vaccine in high dosage
- OTHER
-
Placebo
Participants will receive one dose of normal saline.
Sponsors & Collaborators
-
Sinovac Biotech Co., Ltd
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2026-03-09
- Primary Completion
- 2026-06-30
- Completion
- 2027-05-30
Countries
- China
Study Locations
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