Sanofi gets priority U.S. FDA review for sutimlimab product

Sanofi gets priority U.S. FDA review for sutimlimab product
Reuters: Health
French healthcare company Sanofi said on Thursday that the U.S. Food & Drug Administration (FDA) regulator had granted a priority review for Sanofi's sutimlimab product, which treats hemolysis in adults suffering from cold agglutinin disease.


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