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Merck's RSV antibody showed strong results in young children, supporting extended protection and FDA approval.
Merck announced positive Phase 3 SMART trial results for its RSV monoclonal antibody Enflonsia (clesrovimab) in children under two, showing sustained safety and effective serum levels supporting a second dose for extended protection into a second RSV season.
The data, along with prior findings, underpinned the FDA’s 2025 approval for use in infants during their first RSV season.
GSK reported its RSV vaccine AREXVY was 75.6% effective against hospitalization after about five months, with early signs of cardiovascular benefit.
Merck’s stock rose 42% over the past year, trading near its 52-week high with analysts maintaining a Buy rating.
El anticuerpo RSV de Merck mostró fuertes resultados en niños pequeños, lo que respalda una protección extendida y la aprobación de la FDA.