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

No results posted yet for this study

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

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07418229 on ClinicalTrials.gov