FDA now approves Esperion's bempedoic non-statin LDL-cholesterol lowering combo

27 February 2020

USA-based Esperion Therapeutics (Nasdaq: ESPR) last week received its first-ever product approval and yesterday announced another, with the US Food and Drug Administration approving Nexlizet (bempedoic acid and ezetimibe) tablet, an oral, once-daily, non-statin LDL-Cholesterol (LDL-C), lowering medicine.

Esperion’s shares gained 2.6% to $58.30 in after-hours trading on Wednesday, but were down 10.57% at $57.05 in pre-market trading today.

Nexlizet is indicated as an adjunct to diet and maximally tolerated statin therapy for the treatment of adults with heterozygous familial hypercholesterolemia (HeFH) or established atherosclerotic cardiovascular disease (ASCVD), who require additional lowering of LDL-C.

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