Merck Announces U.S. FDA Approval of VAXNEUVANCE for the Prevention of Invasive Pneumococcal Disease in Adults 18 Years and Older Caused by 15 Serotypes
Clinical Data Supporting Approval Demonstrated Non-Inferior Immune Responses for the Serotypes Shared with PCV13 VAXNEUVANCE Elicited Superior Immune Responses for Serotypes 3, 22F and 33F Compared to PCV13, Which Are Major Causes of Disease known as MSD outside the United States and Canada, today announced the U.S. Food and Drug Administration approved VAXNEUVANCE ™ for active immunization for the prevention of … Clinical Data Supporting Approval Demonstrated Non-Inferior Immune Responses...
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