Merck & Company IncFDA and EMA accepted supplemental applications to expand RSV antibody use in children, a regulatory milestone.

Merck has secured acceptance from both the FDA and the European Medicines Agency for supplemental applications to expand the use of its antibody ENFLONSIA for preventing RSV in young children at elevated risk. The filings seek to broaden the indication into vulnerable pediatric groups where preventative options remain limited. The dual regulatory milestones underscore Merck's efforts to diversify its portfolio beyond oncology as attention on the future of Keytruda intensifies. A key signpost will be the FDA's March 22, 2027 PDUFA decision on the supplemental Biologics License Application, alongside the EMA outcome, which will determine whether this potential second-season use can become a meaningful pediatric RSV franchise.
Merck & Company IncFDA and EMA accepted supplemental applications to expand RSV antibody use in children, a regulatory milestone.
Merck KGaA