Esperion
- Company typePublic
- Founded1998
- HeadquartersAnn Arbor, United States
- Headcount251–500
- GTM typeB2B
- OfferingHardware or Manufacturing
What Esperion does
Esperion Therapeutics is a commercial-stage biopharmaceutical company headquartered in Ann Arbor, Michigan, that develops and markets oral, non-statin lipid-lowering therapies for cardiovascular disease. The company was founded in 2008 by Dr. Roger S. Newton around bempedoic acid — the first and only FDA-approved ATP-citrate lyase (ACLY) inhibitor — acquired from Pfizer along with worldwide patent rights. Its commercial portfolio consists of NEXLETOL (bempedoic acid monotherapy) and NEXLIZET (bempedoic acid/ezetimibe combination), both approved in the U.S. and Europe for LDL-C reduction in statin-intolerant and high-risk cardiovascular patients, and most recently expanded via the March 2026 acquisition of Corstasis Therapeutics to include Enbumyst (bumetanide nasal spray), the first FDA-approved nasal spray loop diuretic.
The company monetizes through a dual-channel model: direct U.S. commercial operations with a field sales force targeting cardiologists, lipidologists, and primary care physicians (FY2025 U.S. net product revenue of $159.6M, 38% YoY growth) complemented by a global partnership network for international markets — Daiichi Sankyo Europe (30+ countries), Otsuka Japan, HLS Therapeutics Canada, CSL Seqirus Australia/NZ, and Neopharm Israel. Total FY2025 revenue reached $403.1 million (21% YoY growth), inclusive of $243.6M in collaboration revenue spanning royalties, milestones (notably a $90M Otsuka payment tied to Japan launch), and product supply. The pipeline includes ESP-2001, a next-generation allosteric ACLY inhibitor in preclinical development for primary sclerosing cholangitis, and the company holds composition-of-matter patent protection through 2030 in the U.S. and settlement agreements restricting ANDA generic entry until April 2040.
Esperion operates as a public company on NASDAQ under ticker ESPR, but in May 2026 ARCHIMED agreed to acquire the company for approximately $1.1 billion ($3.16 per share plus up to $100M in contingent value), with closing expected in Q3 2026 and a consequent delisting. The current headcount range is 251-500 employees, and the company holds Class 1 guideline recommendations from 2026 ACC/AHA and ESC/EAS 2025 positioning bempedoic acid alongside PCSK9 inhibitors in standard lipid management.
Esperion firmographics
Firmographics- Name
- Esperion
- Legal name
- Esperion Therapeutics, Inc.
- Website
- http://www.esperion.com
- Company type
- Public
- Founded year
- 1998
- Operating status
- Operating
- Headcount range
- 251–500 employees
- Ownership category
- akta.pro rank
Esperion industry classification
Industry- Product category
- Cardiovascular Pharmaceuticals
- NAICS
- Drugs and Druggists' Sundries Merchant Wholesalers (4242)
- SIC
- Medicinal Chemicals & Botanical Products (2833)
- akta.pro primary industry
- Cardiology & Vascular Specialty Pharmaceuticals (HLAIACAG)
Keywords
Where Esperion is headquartered
LocationHeadquarters
- HQ city
- Ann Arbor
- HQ country
- United States
- HQ region
- North America
Offices1 record
Markets served
Esperion business model
Business model- GTM type
- B2B
- Offering type
- Hardware or Manufacturing
- Cost components
- Marketing or Sales, Personnel, Technology or R&D, Operations, Supply Chain
Revenue model
- U.S. Product Sales: Direct net product revenue from sales of NEXLETOL (bempedoic acid) and NEXLIZET (bempedoic acid/ezetimibe combination) in the United States. Q4 2025 U.S. net product revenue was $43.7 million, growing 38% year-over-year. Full year 2025 U.S. net product sales reached $159.6 million.
- Collaboration Revenue: Revenue from international partners including royalty payments, milestone payments, and product sales to partners. Q4 2025 collaboration revenue was $124.7 million (including $90M Otsuka milestone). Full year 2025 collaboration revenue was $243.6 million. Royalty revenue from Daiichi Sankyo Europe was $14.6 million in Q4 2025, up 51% year-over-year.
- Milestone Payments: One-time payments from partners upon regulatory approvals and commercial launches. Esperion received $90 million from Otsuka following Japan regulatory approval and favorable NHI price listing for NEXLETOL.
- Royalty Monetization: Sale of royalty interests to capital partners. Esperion sold Japan royalty rights for $50 million to Athyrium Capital Management to fund the Corstasis acquisition. Transaction involves tiered royalties from 12% to 33% until 2x ROI, after which rights revert to Esperion.
Go-to-market motion2 records
Distribution channels7 records
Marketing channels10 records
Esperion product offering
Product offeringCore offering
Esperion is a commercial-stage biopharmaceutical company that develops and commercializes FDA-approved oral non-statin LDL-cholesterol lowering therapies—NEXLETOL (bempedoic acid) and NEXLIZET (bempedoic acid/ezetimibe)—for cardiovascular risk reduction in statin-intolerant patients. Through its 2026 Corstasis Therapeutics acquisition, Esperion also markets Enbumyst (bumetanide nasal spray), the first FDA-approved nasal spray loop diuretic for edema in heart failure, hepatic, and renal disease. Internationally, bempedoic acid products are commercialized as NILEMDO and Nustendi through regional partners.
Product overview
Esperion is a commercial-stage biopharmaceutical company with two FDA-approved oral non-statin therapies for cardiovascular disease: NEXLETOL (bempedoic acid) and NEXLIZET (bempedoic acid/ezetimibe combination). In 2026, Esperion expanded its portfolio through the acquisition of Corstasis Therapeutics, adding Enbumyst (bumetanide nasal spray) - the first FDA-approved nasal spray loop diuretic for edema. The company is also developing ESP-2001, a next-generation ACLY inhibitor for primary sclerosing cholangitis. Internationally, bempedoic acid is marketed as NILEMDO and Nustendi through partnerships with Daiichi Sankyo Europe and HLS Therapeutics.
Differentiator
Problem solved
Functional benefit
Brands
- NEXLETOL: FDA-approved bempedoic acid tablet for reducing LDL-C in adults with hypercholesterolemia, including heterozygous familial hypercholesterolemia (HeFH).
- NEXLIZET
- Enbumyst
- ESP-2001
- NILEMDO
- Nustendi
Products and services
- NEXLETOL (bempedoic acid) Oral, once-daily, first-in-class non-statin LDL-C lowering therapy for adults with hypercholesterolemia inadequately treated with statins. First and only FDA-approved ATP citrate lyase (ACLY) inhibitor for cardiovascular risk reduction. Targets statin-intolerant patients with proven cardiovascular event reduction in the CLEAR Outcomes trial.
- NEXLIZET (bempedoic acid and ezetimibe) Combination tablet containing bempedoic acid plus ezetimibe for enhanced LDL-C reduction in adults with hypercholesterolemia, including heterozygous familial hypercholesterolemia. Combines two complementary mechanisms (ACLY inhibition and cholesterol absorption inhibition) to deliver 38% additional LDL-C reduction beyond statin or bempedoic acid monotherapy.
- Enbumyst (bumetanide nasal spray) First and only FDA-approved nasal spray loop diuretic (bumetanide) for outpatient treatment of edema associated with congestive heart failure, hepatic disease, and renal disease in adults. Provides rapid onset of action and addresses an estimated $4 billion+ U.S. market opportunity across the 6.7 million American adults living with congestive heart failure.
- NILEMDO (bempedoic acid) - International Brand European brand of bempedoic acid marketed by Daiichi Sankyo Europe and HLS Therapeutics (Canada) for LDL-C reduction in patients with hypercholesterolemia and cardiovascular risk. Commercialized through Esperion's international partnership network covering 30+ European countries.
- Nustendi (bempedoic acid and ezetimibe) - International Brand European brand of the bempedoic acid and ezetimibe combination tablet commercialized by Daiichi Sankyo Europe for LDL-C reduction in patients at risk of cardiovascular disease.
- ESP-2001 (preclinical pipeline candidate) Preclinical development candidate—a highly specific next-generation allosteric ATP-citrate lyase (ACLY) inhibitor—being developed for the treatment of primary sclerosing cholangitis (PSC), a rare progressive liver disease with no approved treatments affecting approximately 76,000 diagnosed patients in the U.S. and Europe. Potential Orphan Drug and Fast Track designations expected with IND filing anticipated in 2026.
Quantifiable outcome
- 42% reduction in venous thromboembolism risk with bempedoic acid treatment in CLEAR Outcomes post-hoc analysis
- +7 more outcomes
Companies that use Esperion
Customer profileSegments5 records
Ideal customer profiles4 records
Esperion technology and API
TechnologyTechnology focussed No
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature5 records
Esperion partnerships and signals
Strategic signalPartnerships
Six partnerships are on record, tiered core, minor and strategic.
- Corstasis TherapeuticscoreEsperion acquired Corstasis Therapeutics for $75 million upfront cash plus up to $180 million in milestone payments and low double-digit royalties. The acquisition brings Enbumyst (bumetanide nasal spray), the first FDA-approved nasal spray loop diuretic for edema associated with heart failure, into Esperion's cardiovascular franchise. The transaction targets a U.S. market exceeding $4 billion and is expected to close Q2 2026, subject to customary closing conditions.
- CSL SeqirusminorCSL Seqirus is Esperion's partner for Australia and New Zealand. Filed marketing application for NEXLETOL and NEXLIZET in Australia in July 2025, with expected market approval in Q4 2026.
- HLS TherapeuticsstrategicHLS Therapeutics in-licensed exclusive Canadian rights to NILEMDO and NEXLIZET from Esperion in May 2025. NILEMDO received Health Canada approval and launched commercially in March 2026 targeting over 500,000 statin-intolerant Canadians. NEXLIZET approval expected in 2027.
- Neopharm IsraelminorNeopharm Israel is Esperion's partner for the Israeli market. Regulatory approval for NEXLETOL and NEXLIZET expected in first half of 2026.
- Daiichi Sankyo EuropecoreDaiichi Sankyo Europe commercializes NILEMDO (bempedoic acid) and NUSTENDI (bempedoic acid/ezetimibe) across the European Economic Area, UK, Turkey, and Switzerland. Partnership expanded in April 2021 to include S. Korea, Taiwan, Hong Kong, Thailand, Vietnam, Brazil, and other markets. Products launched in 30+ countries with double-digit annual growth and 700,000+ patients treated.
- Otsuka Pharmaceutical CompanycoreOtsuka manages development, regulatory approvals, and commercialization of bempedoic acid in Japan. Total agreement value of $600 million including milestones and development costs, with significant royalties on net sales. NEXLETOL received regulatory approval and NHI pricing in late 2025, triggering $90 million payment to Esperion with commercial launch underway.
Scale indicators14 records
Recent moves7 records
Expansion highlights7 records
Esperion competitors and assessment
Company assessmentBroad incumbents
- Amgen: Global biopharma with Repatha (evolocumab), a leading PCSK9 inhibitor for LDL-C lowering. Competes directly with bempedoic acid in statin-intolerant/high-risk patients but operates at much larger scale across multiple therapeutic areas.
- Novartis: Markets Leqvio (inclisiran), a siRNA-based PCSK9-targeting therapy for LDL-C lowering. Represents an emerging non-statin alternative competing for the same cardiologist/lipidologist prescribing workflow, though Novartis operates a much broader pharmaceutical portfolio.
- Pfizer: Original developer and licensor of bempedoic acid before spinning out Esperion; Pfizer markets Lipitor and broader cardiovascular portfolio. Historical and structural relationship with Esperion, and competes for cardiologist prescription share through established statin franchise.
- Regeneron Pharmaceuticals: Commercializes Praluent (alirocumab) in partnership with Sanofi as a PCSK9 inhibitor for LDL-C reduction. Direct competitor in lipid management, complemented by broader ophthalmology, oncology, and immunology franchises.
Others
- Otsuka Pharmaceutical: Japanese pharma partner commercializing NEXLETOL in Japan following late-2025 launch. Distribution partner and major collaboration-revenue contributor ($90M milestone in 2025) rather than direct competitor; comparable in cardiovascular commercial infrastructure scale.
- HLS Therapeutics: Canadian specialty pharma commercializing NILEMDO/NEXLIZET under license from Esperion. Adjacent ecosystem participant and distribution partner rather than direct competitor; relevant for understanding Canadian commercial economics.
Direct peers
- Madrigal Pharmaceuticals: Commercial-stage specialty biopharma with Rezdiffra (resmetirom) for MASH, a cardiometabolic/liver disease therapy. Comparable specialty-pharma commercial model targeting metabolic-disease specialists, with similar launch-stage growth profile.
- Amarin Corporation: Cardiovascular-focused specialty pharma commercializing Vascepa (icosapent ethyl) for cardiovascular risk reduction. Comparable in cardiovascular specialty pharma commercial model, prescriber focus on cardiologists, and lipid/risk-reduction therapeutic category.
- NewAmsterdam Pharma: Late-stage clinical biopharma developing obicetrapib, an oral CETP inhibitor for LDL-C lowering in high-risk cardiovascular patients. Direct competitor to bempedoic acid in the same statin-intolerant and high-risk patient segments targeted by NEXLETOL/NEXLIZET.
Emerging players
- Ionis Pharmaceuticals: Develops antisense-based therapies including olpasiran for elevated Lp(a) and other cardiometabolic targets. Relevant as an emerging player in next-generation lipid-lowering with overlapping prescriber audience and complementary mechanism.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat5 records
Key risks6 records
Key highlights7 records
Customer concentration
Esperion social profiles
Digital presenceEsperion financial estimates
Financial estimateRevenue estimate
Valuation estimate
Esperion leadership team
Management profileNumber of profiles
Profiles6 records
Esperion subsidiaries and ownership
Company hierarchySubsidiaries1 record
Esperion funding detail
Funding detailFunding overview
Funding rounds12 records
Investors10 records
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Esperion M&A and investment
M&A and investmentM&A1 record
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about Esperion
What does Esperion do?
Esperion is a commercial-stage biopharmaceutical company that develops and commercializes FDA-approved oral non-statin LDL-cholesterol lowering therapies—NEXLETOL (bempedoic acid) and NEXLIZET (bempedoic acid/ezetimibe)—for cardiovascular risk reduction in statin-intolerant patients. Through its 2026 Corstasis Therapeutics acquisition, Esperion also markets Enbumyst (bumetanide nasal spray), the first FDA-approved nasal spray loop diuretic for edema in heart failure, hepatic, and renal disease. Internationally, bempedoic acid products are commercialized as NILEMDO and Nustendi through regional partners.
Is Esperion a public or private company?
Esperion is a public company. It is classified as public and is currently operating.
When was Esperion founded?
Esperion was founded in 1998. It employs 251 to 500 people.
Where is Esperion based?
Esperion is headquartered in Ann Arbor, United States, in the North America region.
How does Esperion make money?
Four revenue lines are on record. U.S. Product Sales are the primary driver. The others are collaboration Revenue, milestone Payments and royalty Monetization.
Who are Esperion's main competitors?
Broad incumbents on record are Amgen, Novartis, Pfizer and Regeneron Pharmaceuticals. Others are Otsuka Pharmaceutical and HLS Therapeutics. Direct peers are Madrigal Pharmaceuticals, Amarin Corporation and NewAmsterdam Pharma. Ionis Pharmaceuticals is listed as an emerging player.
Does Esperion have an API?
No public API is recorded for Esperion.
What industry is Esperion in?
Esperion's product category is Cardiovascular Pharmaceuticals. Its primary akta.pro industry code is HLAIACAG, Cardiology & Vascular Specialty Pharmaceuticals. Its NAICS code is 4242 and its SIC code is 2833.