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The EU's top drug panel recommended approval for Merck's Keytruda and a new RSV shot for infants, pending final EU decision.
The European Medicines Agency's CHMP has recommended approval for Merck's cancer drug Keytruda in a subcutaneous form for all adult EU indications and for treating certain adults with resectable head and neck cancer.
The committee also recommended approval for Enflonsia, Merck's RSV preventive for infants, which would be the first and only RSV option in Europe using a single dose for all infants regardless of weight.
Both recommendations are pending final review by the European Commission, with decisions expected by year-end.
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El máximo panel de medicamentos de la UE recomendó la aprobación de Keytruda de Merck y una nueva vacuna contra el RSV para los bebés, a la espera de una decisión final de la UE.