FDA Approves Xocova as First Oral Post-Exposure Covid-19 Prevention Therapy
The Food and Drug Administration (FDA) approved Shionogi’s Xocova as the first oral post-exposure therapy for the prevention of Covid-19. This approval marks a significant advancement in Covid-19 prevention treatments.
The FDA’s decision signifies a new approach to managing Covid-19, providing an oral option for individuals seeking to prevent the virus after potential exposure. Xocova’s approval introduces a convenient method for post-exposure prophylaxis, potentially reducing the severity and spread of the disease.
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Date: June 1, 2026
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