drugset / Trial / NCT07208461

A Study to Evaluate the Immunogenicity and Safety of a Recombinant Respiratory Syncytial Virus Vaccine in Older Adults Aged 60 Years and Older

NCT07208461

Phase 2 Active not recruiting 700 enrolled Guangzhou Patronus Biotech Co., Ltd.
RandomizedParallel-groupQuadruple-blindPrevention

Summary

This is a randomized, observer-blinded, placebo-controlled Phase Ⅱ clinical trial to evaluate the immunogenicity and safety of the Respiratory Syncytial Virus (RSV) Vaccine, LYB005 in participants aged 60 years and older.

Timeline

Start
2025-10-21
Primary completion
2026-03
Completion
2026-12

Drugs

EvaluationDrugModalityDoseRoute
Subject LYB005 Vaccine 30 ug
Subject LYB005 Vaccine 60 ug
Subject LYB005 Vaccine 120 ug