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Active, not recruiting Observational

Comparison of Two Methods of Immunoprophylaxis Against RSV in Term Newborns

NCT07251972 · tracked via the Priya Life Science France tracker
Sponsor
Jean-Michel HASCOET
Phase
Observational
Started
2025-09-01
Last updated
2025-11-26

Condition(s) studied

Bronchiolitis

Investigational drug(s) / intervention(s)

to compare vaccine and monoclonal antibody

to compare vaccine and monoclonal antibody: collect the details at birth of chosen immunoprophylaxis and collect if later there will be any hospitalisation for bronchiolitis or consultation emergencies

Study summary

Bronchiolitis is a lower respiratory tract infection, extremely common in pediatrics, and potentially serious. Bronchiolitis affects nearly 30% of infants under 2 years old each year, representing approximately 480,000 cases annually worldwide. Each year, 2 to 3% of infants under 1 year old are hospitalized for bronchiolitis. The virus primarily found worldwide and in France is RSV. Given the scale, frequency, and potential severity of the illness, several immunoprophylaxis methods have been developed.

Currently, there are two methods: the ABRYSVO vaccine, administered to pregnant women during the last month of pregnancy for immunization via the placenta through the transplacental passage of anti-RSV-A and RSV-B antibodies; or neonatal immunoprophylaxis with BEYFORTUS, which involves an intramuscular injection of the monoclonal antibody nirvesimab directly into the newborn immediately before discharge from the maternity ward during the epidemic period.

Currently, no superiority or difference has been described for either immunoprophylaxis method.

Eligibility

Sex
ALL
Min age
4 Days
Max age
8 Months
Healthy volunteers
No
Inclusion Criteria: * all term born neonates Exclusion Criteria: * postnatal transfert * born at home or in birthing center

Primary outcome measure(s)

  • Bronchiolitis incidence — 8 months
    Number of emergency room visits for bronchiolitis

Trial sites (1)

FacilityCityRegionStatus
Chru Nancy Nancy France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07251972 on ClinicalTrials.gov ↗ ← All trials in France