Merck Says FDA Approves ENFLONSIA For Prevention Of RSV Lower Respiratory Tract Disease In Neonates And Infants Who Are Born During Or Entering First RSV Season

Merck & Co., Inc. -0.79%

Merck & Co., Inc.

MRK

83.36

-0.79%

ENFLONSIA is a preventive monoclonal antibody designed to protect infants against a spectrum of RSV disease severity, including worsening disease requiring hospitalization

ENFLONSIA is the first and only RSV preventive option administered to infants using the same dose regardless of weight

Merck (NYSE:MRK), known as MSD outside of the United States and Canada, today announced the U.S. Food and Drug Administration (FDA) has approved ENFLONSIA™ (clesrovimab-cfor) for the prevention of respiratory syncytial virus (RSV) lower respiratory tract disease in neonates (newborns) and infants who are born during or entering their first RSV season. ENFLONSIA is a preventive, long-acting monoclonal antibody (mAb) designed to provide direct, rapid and durable protection through 5 months, a typical RSV season, with the same 105 mg dose regardless of weight. A typical RSV season usually spans autumn to spring of the next year.

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