French healthcare company Sanofi S.A. (Euronext Paris:SAN) (Nasdaq:SNY) reported on Monday that a universal respiratory syncytial virus immunisation programme using Beyfortus (nirsevimab) was associated with a statistically significant reduction in RSV-related hospitalisations in the second RSV season among infants immunised during their first season.
Conducted in Galicia, Spain, the real-world population study evaluated outcomes across two consecutive RSV seasons. Findings have been published in The Lancet Infectious Diseases, and will be presented at the RSVVW '26 conference in Rome, Italy.
Coverage reached 94.4% (11,796 of 12,492 eligible infants), with an 85.9% reduction in RSV-related lower respiratory tract infection hospitalisations in the first season and 55.3% fewer hospitalisations in the second season among infants immunised during infancy.
The analysis also showed reductions in first-season primary care consultations, including 30.8% for acute bronchitis or bronchiolitis, 33.4% for lower respiratory tract infections, and 27.7% for wheezing or asthma. Among infants previously hospitalised due to RSV, second-season rehospitalisations declined by 78.2% for RSV-related cases and 62.4% for lower respiratory tract infections. The data support the hypothesis that preventing severe RSV infection during early lung development may make infants less prone to subsequent admissions from either RSV or other infections.
ALK secures EU approval for EURneffy 1 mg as needle-free adrenaline option for children
4DMedical secures EU approval for CT:VQ as EUR83m funding fuels European expansion
AstraZeneca's tozorakimab meets primary endpoints in two Phase III COPD trials
Eisai and Nuvation Bio report taletrectinib MAA validated by European regulator
Akeso's Phase II trials of AK146D1 and AK138D1 approved in China
UCB selects PANTHERx Rare to distribute KYGEVVI for TK2d
Roche launches new test to help clinicians treat patients with respiratory infections
GSK secures Japan Orphan Drug status for lung cancer ADC
Dizal meets primary endpoint in Phase 3 study of ZEGFROVY (sunvozertinib) monotherapy
bioMérieux secures IVDR CE marking for respiratory diagnostic panels in Europe
Avacta opens Phase 1 trial for AVA6103 cancer therapy in US
IDEAYA Biosciences enrols first patient in Phase 1 trial of PRMT5 inhibitor IDE892
Airiver Medical's Airiver Pulmonary DCB receives US FDA Breakthrough Device Designation