US FDA Accepts sBLA for ENFLONSIA to Expand RSV Indication
US Food and Drug Administration (FDA) and European Medicines Agency (EMA) accept applications for ENFLONSIA (clesrovimab-cfor) to expand RSV protection for high-risk children under 2 years of age during their second Respiratory Syncytial Virus (RSV) season.
Merck ENFLONSIA | 07/08/2026 | By News Bureau
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