RSV Antiviral Zelicapavir Enters Late-stage Clinical Trials
Enanta Pharma advanced zelicapavir into a registrational Phase 2b/3 clinical trial for adults at high risk of severe RSV outcomes.
Enanta Pharma advanced zelicapavir into a registrational Phase 2b/3 clinical trial for adults at high risk of severe RSV outcomes.
Enanta Pharma advanced zelicapavir into a registrational Phase 2b/3 clinical trial for adults at high risk of severe RSV outcomes.
Read MoreThe FDA approved the first generic of Xofluza (baloxavir marboxil) tablets, the first single-dose treatment for acute uncomplicated influenza and prophylaxis in patients 5 years of age and older.
Read MoreResearchers found that sialidase inhibitors—a class of flu drugs including oseltamivir (Tamiflu)—protected against degradation of protective sugar molecules tied to cognitive decline and premature aging in people living with HIV.
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 MoreA two-week course of metformin or ursodeoxycholic acid (UDCA) did not meaningfully improve recovery from long COVID symptoms.
Read MoreThe American College of Physicians (ACP) issued its final update on antiviral treatment for COVID‑19 in outpatient settings.
Read MoreResearchers investigated the safety and efficacy of Paxlovid (nirmatrelvir/ritonavir) for hemodialysis-dependent patients with COVID-19.
Read MoreNew research discovered that data used in the development of SARS-Cov-2 antivirals contained major errors.
Read MoreThe FDA approved Enflonsia, a long-acting monoclonal antibody designed to protect neonates and infants from RSV-related lower respiratory tract disease.
Read MoreIn laboratory testing, new drug candidate Jun13296 remained effective against Paxlovid-resistant strains of the coronavirus SARS-CoV-2.
Read MoreTwo FDA–approved flu antivirals did not successfully treat severe H5N1 infections, and route of infection (eye, nose or mouth) significantly impacted effectiveness.
Read MorePaxlovid does not significantly reduce COVID-19 hospitalization and mortality among vaccinated older adults, according to UCLA-led research.
Read MoreA new antiviral modeling approach combines various experimental techniques to create a comprehensive picture of a virus’ dynamic behavior.
Read MoreThe online tool provides weekly updates on flu activity across states and cities, highlighting regions with the highest increases and historical trends.
Read MorePneumonia is a potentially life-threatening infection of the lungs that inflames alveoli and spurs the overproduction of purulent material. Typically afflicting neonates and seniors, the COVID pandemic has revealed the importance of proper pneumonia care for all patients.
Read MoreTopline results demonstrated that the drug was well-tolerated over a 10-day period and achieved consistent plasma levels without the need for ritonavir co-administration.
Read MoreFuture updates to COVID-19 treatment recommendations will transition to professional medical societies.
Read MoreA new case report sheds light on the first documented transmission of bird flu from cow to human.
Read MoreUH15-38 shows potential in preventing lung injury and reducing inflammation in severe influenza when administered even five days after infection.
Read MoreResearchers identified unusual COVID-19 mutation patterns that were strongly associated with molnupiravir use and coincided with the drug’s introduction.
Read MoreIn this 2023 update of RT’s pharmacological treatment of respiratory disorders, the most commonly administered classes of pulmonary medications are reviewed.
Read MorePfizer’s Paxlovid is the fourth drug—and first oral antiviral pill—approved by the FDA to treat COVID-19 in adults.
Read MoreResearchers identified potential broad-spectrum antiviral agents that can target multiple families of RNA viruses that pose a significant threat for future pandemics.
Read MoreThe oral, direct-acting antiviral drug candidate is being evaluated in the global phase 3 SUNRISE-3 registrational trial for the treatment of COVID-19 in outpatients at high risk for disease progression regardless of vaccination status.
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