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Merck & Co Makes Case For Molnupiravir After Narrow FDA Nod

Backing Comes Day After Pfizer's Paxlovid Green Light

 
• By Nielsen Hobbs

US regulators have granted emergency authorization to the antiviral molnupiravir but only for use when "alternative COVID-19 treatment options authorized by the FDA are not accessible or clinically appropriate."

Merck_New_Jersey
• Source: Archive

The timing of the US Food and Drug Administration’s emergency use authorization for Merck & Co., Inc.’s COVID-19 treatment molnupiravir appears to have allowed the agency to craft a less complicated indication – though still not one that’s particularly favorable to the product.

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