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Safety and Immunogenicity of the Recombinant Respiratory Syncytial Virus (RSV) Vaccine in Adults Aged 18 Years and Older

StatusActive, Not Recruiting
PhasePhase 1
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated August 22, 2025 (before its estimated August 2026 completion). Its status may not reflect the trial's current state.

Record History

  1. Minor Trial status: Not Yet Recruiting to Active, Not Recruiting
    • Start date changed from estimate of Apr 14, 2025 to Apr 15, 2025
    • Site contact updated
    v2
  2. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This phase 1 study in China will evaluate the safety and immunogenicity of the the Respiratory Syncytial Virus (RSV) Vaccine, LYB005 in adults aged 18 years and older.
Trial Details
NCT Number NCT06904222
Lead Sponsor Guangzhou Patronus Biotech Co., Ltd.
Conditions
(from sponsor)
Respiratory Syncytial Virus Infection
Related terms Respiratory Syncytial Virus Infections
Enrollment 90 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov