Repeated Cross Sectional Surveillance Study To Determine the Respiratory Syncytial Virus (RSV) Immunization Rates in German Infants

NCT06824207 | Active Not Recruiting

• 1 other identifier: RSV00093
• Study Type: observational
• Target: 2,400
• Locations: 1 country
• Sites: 1

Brief Summary

In June 2024, the German Standing Committee on Vaccination (STIKO) recommended the universal immunization of infants with nirsevimab during their first RSV season. Nirsevimab is a long-acting monoclonal antibody designed to provide passive immunity against RSV, significantly reducing the risk of severe RSV disease in infants. This recommendation marks the 2024/25 season as the first in which nirsevimab is broadly implemented for all infants in Germany. Despite the introduction of this new prevention measure, there is currently no timely monitoring system for immunization rates. Understanding the uptake and coverage of nirsevimab is crucial for evaluating its impact on public health and guiding future vaccination strategies. Therefore, this study aims to monitor the national immunization rates of nirsevimab in children under one year of age during the initial seasons of its widespread use. The primary objective of this study is to determine the Nirsevimab immunization rate in eligible infants in their first RSV-season in Germany. The study will focus on:

1. 1.Assessing the immunization rates among eligible infants (according to STIKO recommendation) in their first RSV-season in Germany (i.e. across all geographies)
2. 2.Assessing the immunisation rates among the "catch-up cohort", i.e. all infants born between April and September. For these infants, the STIKO recommends immunization with nirsevimab in early autumn.
3. 3.Assessing the immunization rate among the "in-season cohort", i.e. all infants born during the RSV season between October and March. For these newborns, the STIKO recommends immunization with Nirsevimab shortly after birth, preferably during the second "well-baby visit" at the age of 3-10 days of life.

Conditions

Respiratory Syncytial Virus Immunization

Keywords

RSV; RSV Immunization Rates; Nirsevimab

Outcome Measures

Primary Outcomes (1)

• Assessing the nirsevimab immunization rates among eligible infants in both cohorts

  Descriptive analysis of nirsevimab immunization status (yes/no) will be performed using summary statistics, i.e., proportion of immunized infants among all enrolled infants per wave.

  Throughout Study (Approximatley 4 months)

Secondary Outcomes (4)

• Assessing the seasonal evolution of the nirsevimab immunization coverage rates among the two cohorts

  Throughout Study (Approximatley 4 months)

• Assessing reasons for/against nirsevimab immunization

  Throughout Study (Approximately 4 months)

• Assessing the nirsevimab immunization rates among subgroups

  Throughout Study (Approximately 4 months)

• Assessing the reliability of a demographic study

  Throughout the Study (Approximately 4 months)

Study Arms (2)

Catch-Up Cohort

Parents of infants born between April and September

In-Season Cohort

Parents of infants born between October and March

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

This study is conducted using various recruitment approaches, including but not limited to mailings, online panels, telephone contact, in person contact. The data i.e. respondents answers will be captured via an online questionnaire. The interviews will be conducted applying various methodologies e.g. self-completion (CAWI), assisted in person completion (F2F interviews), assisted telephone completion (CATI). The study will target a sample of parents of infants either born between April and September (catch-up cohort) or between October and March (in-season cohort). The study targets a representative distribution with regards to both aforementioned subgroups and regions. To achieve the primary objective in the representative sample of the German population of eligible parents, a needed sample size of approximately 2,400 participants in total per season is assessed. These are spread over a total of three waves per season, resulting in a sample size of 800 respondents per wave.

You may qualify if:

• Be a parent of an infant born between April 2024/25/26 and March 2025/26/27, respectively
• Reside in Germany at the time of survey completion
• Be at least 18 years old at the time of survey completion.
• Agree with privacy policy and AE (Adverse Event) reporting requirements before proceeding with the survey.
• Read and agree to the ICF (Informed Consent Form) by ticking a box before proceeding with the survey.

You may not qualify if:

• Participation in the study (= completed the survey) in a previous wave of the current season.
• Note: The above information is not intended to contain all considerations relevant to a potential participation in a clinical trial.

Sponsors & Collaborators

• Sanofi Pasteur, a Sanofi Company: lead

Study Sites (1)

Unknown Facility

Germany, Germany, Germany

Location

Study Design

• Study Type: observational
• Observational Model: OTHER
• Time Perspective: CROSS SECTIONAL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: February 7, 2025
• First Posted: February 13, 2025
• Study Start: January 13, 2025
• Primary Completion (Estimated): May 30, 2026
• Study Completion (Estimated): May 30, 2026
• Last Updated: June 5, 2025

Record last verified: 2025-06

Data Sharing

• IPD Sharing: Will share

Locations

DE (1)