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PRALUENT® (ALIROCUMAB) INJECTION RECEIVES FDA APPROVAL TO TREAT CHILDREN WITH GENETIC FORM OF HIGH C

Date postedMarch 11, 2024
in Industry,

TARRYTOWN, N.Y., March 11, 2024 (GLOBE NEWSWIRE) -- Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) announced the U.S. Food & Drug Administration (FDA) has extended the approval of Praluent® (alirocumab) as an adjunct to diet and other low-density lipoprotein cholesterol (LDL-C) lowering therapies to include pediatric patients aged 8 and older with heterozygous familial hypercholesterolemia (HeFH). Read more...

Wegovy® receives FDA approval for cardiovascular risk reduction in adults with known heart disease aDate postedMarch 8, 2024 Medicare plans can now cover Wegovy for patients at risk of heart diseaseDate postedMarch 22, 2024

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