drugset / Trial / NCT05921903

A Study on the Immune Response and Safety of an RSV Vaccine When Given to Adults 18 Years of Age and Above Who Received Lung or Kidney Transplant and Are at an Increased Risk of Respiratory Syncytial Virus Lower Respiratory Tract Disease and Compared to Healthy Adults 50 Years of Age and Above

NCT05921903

Phase 2 Completed 386 enrolled GlaxoSmithKline
RandomizedParallel-groupOpen-labelPrevention

Summary

The purpose of this study is to evaluate the immunogenicity, safety, and reactogenicity of the RSVPreF3 OA investigational vaccine in an immunocompromised (lung and renal transplant recipients) population and assess whether a second dose of the vaccine increases the immune response.

Timeline

Start
2023-07-28
Primary completion
2024-06-25
Completion
2025-05-16

Drugs

EvaluationDrugModalityDoseRoute
Subject RSVPreF3 OA Vaccine 0.5 ml Intramuscular