ESPR—FDA approves Nexletol/Zetia FDC called Nexlizet: https://www.globenewswire.com/news-release/2020/02/26/1991460/0/en/Esperion-Announces-FDA-Approval-of-the-NEXLIZET-bempedoic-acid-and-ezetimibe-Tablet-an-Oral-Once-Daily-Non-Statin-LDL-Cholesterol-Lowering-Medicine.html By incorporating a dual LDL-lowering MoA, Nexlizet can reduce LDL for some patients beyond what can be accomplished with Nexletol monotherapy. Each Nexlizet tablet contains 180mg of Nexletol and 10mg (generic) Zetia. (Zetia has been off-patent in the US for several years.)