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NOT YET RECRUITING
NCT07615192

RSV Immunisation Status in Queensland (Australia)

Sponsor: Sanofi

View on ClinicalTrials.gov

Summary

The primary objective of this study is to determine the nirsevimab immunisation rate in eligible infants (according to Queensland Paediatric Respiratory Syncytial Virus Prevention Program recommendation) in Queensland, Australia. The study will focus on: 1\. Assessing the immunisation rates among eligible infants (born from 1 February 2024 to 15 April 2025) in their first Respiratory Syncytial Virus (RSV)-season in Queensland. Secondary objectives of this study are as follows: 1. To analyse reasons of parents to decide for or against immunisation of their infant with nirsevimab. 1. This objective aims to assess potential influencing factors and evaluate the changes in acceptance across the three cohorts prior and post recommendation. 2. In this regard, demographic factors (e.g. education, income) will be included in the analysis where applicable to gain insights on their potential impact. 2. To assess immunisation rates for further subgroups, e.g. by: a) risk group (defined chronic condition or pre-term birth status), b) regional areas of Queensland. 3. To compare the vaccination coverage rate estimates with data captured via the Australian Immunisation Register.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

1200

Start Date

2026-05-26

Completion Date

2026-07-20

Last Updated

2026-05-29

Healthy Volunteers

Yes

Interventions

BIOLOGICAL

Nirsevimab Respiratory Syncytial Virus monoclonal antibody

This study will not administer any treatment, only observe the treatment as prescribed in real-world clinical practice

Locations (1)

Paratus Clinical Research

Brisbane, Queensland, Australia