Esperion Therapeutics
ESPRESPR · Stock Price
Historical price data
Overview
Esperion Therapeutics' mission is to deliver oral, once-daily, non-statin medicines for patients with elevated LDL-C. Its key achievement is the successful FDA approval and commercialization of bempedoic acid (NEXLETOL) and its combination with ezetimibe (NEXLIZET), establishing a new therapeutic class. The company's strategy combines direct U.S. commercialization with ex-U.S. partnerships to maximize global reach while advancing a pipeline of next-generation lipid-modifying agents. Esperion aims to become a leading cardiometabolic company by addressing broader patient populations and complementary risk factors.
Technology Platform
Liver-targeted prodrug platform centered on ATP citrate lyase (ACL) inhibition, utilizing a liver-specific activation mechanism to reduce LDL-cholesterol synthesis with a favorable muscle safety profile.
Pipeline
22| Drug | Indication | Stage | Watch |
|---|---|---|---|
| Bempedoic Acid / Ezetimibe Oral Tablet + Placebo | Cardiovascular Diseases | Approved | |
| Bempedoic Acid 180 MG Oral Tablet + Bempedoic Acid/Ezetimibe... | Healthy Lactating Women | Approved | |
| Bempedoic acid + Ezetimibe | Hypercholesterolemia | Phase 3 | |
| bempedoic acid | Hypercholesterolemia | Phase 3 | |
| Bempedoic Acid + Ezetimibe + Placebos | Hyperlipidemias | Phase 3 |
FDA Approved Drugs
2Opportunities
Risk Factors
Competitive Landscape
Esperion competes in a stratified market against low-cost generic statins/ezetimibe and potent, injectable PCSK9 inhibitors. Its key differentiators are oral convenience, a demonstrated cardiovascular outcomes benefit, and a muscle-friendly safety profile, positioning it as a preferred adjunctive or alternative therapy for statin-intolerant, high-risk patients.
Company Timeline
Founded in Ann Arbor, United States
FDA Approval: NEXLIZET
FDA Approval: NEXLETOL