Findings presented at IDWeek 2025 emphasize the need to target pneumococcal serotypes that disproportionately affect adults and exhibit resistance to commonly prescribed antibiotics. Merck announced results from a systematic review of 15 studies published between 2015 and 2025 assessing the epidemiology and antimicrobial resistance of pneumococcal serotypes covered by Capvaxive (Pneumococcal 21-valent Conjugate Vaccine) in comparison to those covered by PCV20.
The review incorporated US data from published studies and Centers for Disease Control and Prevention (CDC) Active Bacterial Core Surveillance reports. Results showed that Capvaxive-unique serotypes were more common among adults with pneumococcal disease (PD) than those covered solely by PCV20. In particular, Capvaxive-unique serotypes such as 35B and 23A demonstrated notably high resistance to penicillin and erythromycin. Among adults aged 65 and older, invasive pneumococcal disease caused by Capvaxive-unique serotypes accounted for over three times the prevalence of PCV20-unique serotypes.
"By covering the serotypes responsible for the majority of invasive pneumococcal disease cases in US adults, based on 2018-2022 national-level CDC data, Capvaxive is specifically designed for adults," Paula Annunziato, MD, senior vice president of infectious diseases and vaccines at Merck Research Laboratories, said in a statement. Capvaxive is currently approved in the US, European Union, Japan, and other countries.