IDSA Concerned Over Federal Plan to Overhaul Infectious Disease Research
Leading medical societies warn that proposed changes and funding delays at the National Institutes of Health could disrupt active studies and patient care.
Leading medical societies warn that proposed changes and funding delays at the National Institutes of Health could disrupt active studies and patient care.
Leading medical societies warn that proposed changes and funding delays at the National Institutes of Health could disrupt active studies and patient care.
Read MoreAAP recommendations expand second-season RSV protection criteria for children ages 8 to 19 months, alongside updated infant COVID-19 vaccination recommendations.
Read MoreNew clinical recommendations emphasize the safety and importance of COVID-19, influenza, and RSV vaccines for individuals with weakened immune systems.
Read MoreFDA will review Enflonsia’s ability to protect high-risk children under 2 years of age during their second RSV season.
Read MoreCVS and Walgreens are expanding walk-in access, multi-vaccine scheduling, and respiratory illness testing ahead of peak viral activity.
Read MoreThe National Foundation for Infectious Diseases (NFID) launched an initiative to streamline evidence-based information regarding respiratory disease prevention.
Read MoreCo-Diagnostics submitted a dual 510(k) premarket notification and CLIA Waiver by Application to the FDA for its Co-Dx PCR Flu A/B & RSV multiplex respiratory test.
Read MoreMerck is seeking expand approval for its RSV drug Enflonsia to include children under age two through their second year of risk.
Read MoreAdults with weakened immune systems, particularly transplant recipients, face significant risks of severe illness and death from respiratory syncytial virus (RSV).
Read MoreInfants exposed to viruses by older siblings face a higher risk of hospitalization and long-term socioeconomic challenges, according to new research.
Read MoreA study shows that a loss of immunity caused flu and RSV peaks to occur earlier in the season before returning to pre-pandemic patterns.
Read MoreEnanta Pharma advanced zelicapavir into a registrational Phase 2b/3 clinical trial for adults at high risk of severe RSV outcomes.
Read MoreThe AMDI Fast PCR System provides point-of-care results for RSV, influenza, and COVID-19 in less than 10 minutes.
Read MoreUnderlying chronic conditions and hospital transfers are major indicators of severe disease in pediatric patients with respiratory tract infections.
Read MoreReal-world data published in JAMA Network Open confirm the effectiveness of the RSVpreF vaccine in protecting newborns from respiratory syncytial virus.
Read MoreThe families of two infants who died in the 1960s are suing the federal government alleging the babies received an experimental RSV vaccine without the knowledge or consent of their families, according to a report by The New York Times.
Read MoreMaternal RSV vaccination reduced infants’ hospitalization risk by more than 80% when administered at least 14 days before birth.
Read MoreEnanta Pharmaceuticals will present data on its RSV therapy zelicapavir and on EPS-3903, an oral STAT6 inhibitor, at ATS 2026.
Read MoreVertical ventilation ducts in residential buildings can facilitate the spread of infectious respiratory aerosols in multi-family buildings.
Read MoreThe once-weekly INNA-051 treatment from ENA Respiratory aims to prime the immune system to protect high-risk patients from influenza, RSV, and other respiratory viruses.
Read MoreAn NFID initiative provided evidence-based guidance on influenza, COVID-19, and RSV during the 2025-2026 season.
Read MoreThe new Roche diagnostic test identifies 25 viruses and bacteria to help clinicians provide...
Read MoreThe expanded approval means Arexvy is now indicated for all adults aged 60 and older, and adults aged 18–59 at increased risk for LRTD caused by RSV.
Read MoreThe American College of Physicians recommends an RSV vaccine for all adults age 75 and older.
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