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NCT Number: NCT06180993

Evaluation of the Effectiveness and Impact of Nirsevimab Administered as Routine Immunization

A longitudinal observational study based on routinely collected data on hospital and health care use for RSV infections will be undertaken. The Galician public health registries will be used for data collection including baseline information and follow-up data. Historical data will be retrieved for comparison purposes. The study aims to observe and analyze data from all the eligible children in Galicia for nirsevimab treatment. The number of eligible children is expected to be approximately 14,000 per each RSV season.

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Key information

Age range

1 day–24 month

Sex eligibility

All sexes

Study type

Observational

Primary location

Hospital Clínico Universitario de Santiago de Compostela

Santiago de Compostela, A Coruña, 15707, Spain

Location status: Recruiting

Location contact

Federico Martinón Torres, PhD, MD

CONTACT

[email protected]

+34981955373

About this study

The purpose of this study is to evaluate the impact of nirsevimab in preventing RSV in healthy infants and high-risk children less than 24 months of age at the start of RSV season in Galicia.

The target population to receive nirsevimab is around 14,000 subjects including all healthy newborns during the RSV season, those < 6 months at the start of the season, as well as those < 24 months with comorbidities at the start of the season. Nirsevimab will be administered as part of the immunization program of Galicia and following the implementation plan designed by the Public Health authorities, using the vaccination facilities of the Galician system, i.e., hospitals and primary care centres. Appointments for administration and registration of administered doses will be performed as per usual immunization protocols. The expected coverage with nirsevimab in the target population is expected to be high (>80%).

RSV testing is routinely performed in the hospital and emergency department settings. The Galician Regional Surveillance Information System will retrieve all the existing information of the different electronic databases for new RSV cases detected in Galicia, including hospitalization, primary care, drug administration and immunization. RSV case ascertainment and classification will be per- formed by a specialized clinical team according to pre-established definitions.

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subjects born in Galicia from April 1st, 2023 and March 1st, 2026

Exclusion criteria

  • No specific criteria has been reported

Treatment and study plan

Nirsevimab

Biological

Nirsevimab will be administered administered in a single dose at birth for birth cohort and at the beginning of the campaign for the other cohorts under study

Other names: Beyfortus

Primary outcomes

  1. Incidence of RSV LRTI hospitalization through the RSV season

    Time frame: 8 months (from October to May)

Sponsors and collaborators

Lead sponsor

Federico Martinón Torres

Other

Registry information

Acronym: NIRSE-GAL

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Dec 26, 2023
Registry last updated
Dec 26, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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