Developer docs
API playgroundTry for free, no card

Search company profiles

Esperion

Full company profile

uuid0000dpu

Namestring
Esperion
Legal namestring
Esperion Therapeutics, Inc.
Company typeenum
Public
Founded yearint
1998
Descriptiontext

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.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
251–500
akta.pro rankint
HeadquartersAnn Arbor, United States
HQ citystring
Ann Arbor
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
cardiovascular pharmaceuticals, lipid lowering therapies, LDL cholesterol drugs, biopharmaceutical products, heart failure treatments
Industry1 code
1Cardiology & Vascular Specialty Pharmaceuticals
CodeHLAIACAGPrimaryYes
NAICS code1 code
  • Drugs and Druggists' Sundries Merchant Wholesalers4242
SIC code1 code
  • Medicinal Chemicals & Botanical Products2833
Product category
Cardiovascular Pharmaceuticals
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model4 records
1U.S. Product Sales
TypeOne Time License
Description

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.

esperion.com
2Collaboration Revenue
TypeLicensing Royalties
Description

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.

esperion.com
3Milestone Payments
TypeLicensing Royalties
Description

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.

esperion.com
4Royalty Monetization
TypeLicensing Royalties
Description

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.

za.investing.com
Marketing channels10 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels7 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Marketing or Sales, Personnel, Technology or R&D, Operations, Supply Chain
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 6 records shown
1NEXLETOL
Description

FDA-approved bempedoic acid tablet for reducing LDL-C in adults with hypercholesterolemia, including heterozygous familial hypercholesterolemia (HeFH).

esperion.com
+5 more records
Core offering1 text field

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.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 8 values shown
  • 42% reduction in venous thromboembolism risk with bempedoic acid treatment in CLEAR Outcomes post-hoc analysis
+7 more records
Product overview1 text field

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.

Product and service6 records
1NEXLETOL (bempedoic acid)
CategoryLipid-Lowering Cardiovascular Therapy
Description

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.

2NEXLIZET (bempedoic acid and ezetimibe)
CategoryLipid-Lowering Cardiovascular Therapy
Description

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.

3Enbumyst (bumetanide nasal spray)
CategoryCardiorenal / Heart Failure Therapy
Description

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.

4NILEMDO (bempedoic acid) - International Brand
CategoryLipid-Lowering Cardiovascular Therapy (International)
Description

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.

5Nustendi (bempedoic acid and ezetimibe) - International Brand
CategoryLipid-Lowering Cardiovascular Therapy (International)
Description

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.

6ESP-2001 (preclinical pipeline candidate)
CategoryPipeline - Rare Disease Liver Therapy
Description

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.

Scale indicator14 records

Each record includes

Type, Value, Description, Source

Partnership6 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-03-03
Description

Esperion 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.

Strategic tierMinorTypeChannel Partner/ Reseller/ DistributorAnnounced on2025-07-01
Description

CSL 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.

Strategic tierStrategicTypeChannel Partner/ Reseller/ DistributorAnnounced on2025-05-01
Description

HLS 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.

Strategic tierMinorTypeChannel Partner/ Reseller/ DistributorAnnounced on2025-01-01
Description

Neopharm Israel is Esperion's partner for the Israeli market. Regulatory approval for NEXLETOL and NEXLIZET expected in first half of 2026.

Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2018-01-01
Description

Daiichi 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.

Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2018-01-01
Description

Otsuka 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.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight7 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

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.

TypeOthers
Description

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.

TypeDirect peer
Description

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.

TypeEmerging player
Description

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.

TypeBroad incumbent
Description

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.

TypeDirect peer
Description

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.

TypeOthers
Description

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.

TypeBroad incumbent
Description

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.

TypeBroad incumbent
Description

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.

TypeDirect peer
Description

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.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment5 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile4 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature5 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles6 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

Subsidiaries1 record

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds12 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors10 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A1 record

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Esperion

Cardiovascular Pharmaceuticalsesperion.com

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

  • Cardiovascular pharmaceuticals
  • Lipid lowering therapies
  • LDL cholesterol drugs
  • Biopharmaceutical products
  • Heart failure treatments

Where Esperion is headquartered

Location

Headquarters

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

  1. 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.
  2. 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.
  3. 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.
  4. 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 offering

Core 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 profile

Segments5 records

Ideal customer profiles4 records

Esperion technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature5 records

Esperion partnerships and signals

Strategic signal

Partnerships

Six partnerships are on record, tiered core, minor and strategic.

  • Corstasis TherapeuticscoreStrategic or Co-development Partner · 3 March 2026Esperion 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 SeqirusminorChannel Partner/ Reseller/ Distributor · 1 July 2025CSL 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 TherapeuticsstrategicChannel Partner/ Reseller/ Distributor · 1 May 2025HLS 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 IsraelminorChannel Partner/ Reseller/ Distributor · 1 January 2025Neopharm Israel is Esperion's partner for the Israeli market. Regulatory approval for NEXLETOL and NEXLIZET expected in first half of 2026.
  • Daiichi Sankyo EuropecoreChannel Partner/ Reseller/ Distributor · 1 January 2018Daiichi 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 CompanycoreChannel Partner/ Reseller/ Distributor · 1 January 2018Otsuka 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 assessment

Broad 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 presence

Esperion financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Esperion leadership team

Management profile

Number of profiles

Profiles6 records

Esperion subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

Esperion funding detail

Funding detail

Funding 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 investment

M&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.

Unlock the full company data

50 free credits on sign-up, no credit card required.

Contact sales
Live signals
Stock TitanEsperion settles Renata patent case through 2040Esperion settled patent litigation with Renata, agreeing Renata will not market generic NEXLETOL or NEXLIZET in the U.S. before April 19, 2040, with limited exceptions. Litigation against other generic applicants remains ongoing, with no assurance of generic availability before that date.Stock TitanEsperion launches ENBUMYST nasal spray campaignEsperion Therapeutics is launching a nationwide campaign to raise awareness of ENBUMYST, a nasal spray diuretic for edema in heart failure. The company aims to educate stakeholders ahead of the CMS Ambulatory Specialty Model launching in 2027, which will hold providers accountable for heart failure care costs and quality.Ticker Report521,081 Shares in Esperion Therapeutics, Inc. $ESPR Purchased by Public Employees Retirement System of OhioThe Public Employees Retirement System of Ohio purchased 521,081 shares of Esperion Therapeutics, Inc. valued at approximately $1.43 million in the first quarter, with several other institutional investors also acquiring stakes in the biopharmaceutical company. Esperion reported quarterly earnings of -$0.10 EPS, missing analyst consensus estimates of -$0.02 by $0.08, while revenue of $80.10 million fell short of the $84.52 million forecast. Multiple equity research analysts, including Needham & Company, Citizens JMP, Cantor Fitzgerald, and Piper Sandler, downgraded the stock from buy/strong-buy ratings to hold ratings.Pulse 2.0ARCHIMED Successfully Completes Take-Private of Esperion in $1.1 Billion DealARCHIMED announced the closing of its acquisition of Esperion Therapeutics, a commercial-stage biopharmaceutical company, in a deal valued at approximately $1.1 billion in total equity value on a fully diluted basis. Esperion shareholders are receiving $3.16 per share in cash, representing a 58 percent premium to the closing price prior to the announcement, along with rights to contingent milestone payments of up to $100 million tied to future net sales performance. With the deal closed, Esperion common stock has ceased trading on NASDAQ; ARCHIMED will deploy its MedValue template to accelerate Esperion's growth through product range extension, innovation, licensing, and acquisitions.MarketScreenerAn unknown funds, managed by ArchiMed SAS completed the acquisition of Esperion Therapeutics, Inc. from Wasatch Advisors LP, BlackRock, Inc. and others.Unknown funds managed by ArchiMed SAS completed the acquisition of Esperion Therapeutics, Inc. from Wasatch Advisors LP, BlackRock, Inc. and others on July 13, 2026, for approximately $850 million upfront consideration, with the total transaction valued at up to $1.1 billion on a fully diluted basis including contingent milestone payments of up to $100 million tied to future U.S. net sales performance. Esperion shareholders received $3.16 per share in cash, representing a 58% premium to the closing share price on April 30, 2026, and the company will be delisted from the Nasdaq Stock Market upon closing. The transaction, which had received regulatory clearance from Germany's Bundeskartellamt and U.S. Hart-Scott-Rodino review, was financed in part by up to $400 million in debt financing provided by Pharmakon Advisors, LP and Biopharma Credit.AInvestEsperion Therapeutics Inc. anticipated last trading date July 10, Nasdaq saysNasdaq has announced that July 10, 2026, will be the last trading date for Esperion Therapeutics Inc. (NASDAQ: ESPR), marking the final day the stock will be listed on the exchange. This decision typically precedes delisting, which may result from failure to meet continued listing standards or from mergers, acquisitions, or other corporate actions. Investors are advised to review official communications from the company and Nasdaq regarding the delisting process and potential liquidity risks.PR NewswireAre GBTG, BGMS, SUNE, ESPR Obtaining Fair Deals for their Shareholders?Halper Sadeh LLC, an investor rights law firm, announced investigations into four companies for potential federal securities law violations and breaches of fiduciary duties related to proposed transactions. The companies under scrutiny are Global Business Travel Group (sale to Long Lake Management for $9.50/share), Bio Green Med Solution (merger with Future NRG Sdn. Bhd. ), SUNation Energy (merger with Suniva), and Esperion Therapeutics (sale to ARCHIMED-managed funds for $3.16/share). The law firm stated it may seek increased consideration, additional disclosures, or other relief on behalf of affected shareholders.GurufocusEsperion Therapeutics Investor Alert: Kahn Swick & Foti, LLC InvLaw firm Kahn Swick & Foti, LLC announced an investigation into the proposed acquisition of Esperion Therapeutics, Inc. by funds managed by ARCHIMED, examining whether the consideration of $3.16 per share in cash plus contingent milestone payments adequately values the company. The firm is seeking to determine whether the deal process and terms were fair to Esperion shareholders. This type of shareholder rights investigation is commonly filed when publicly traded companies enter into acquisition agreements.FinancialContent Business PageEsperion Therapeutics Investor Alert: Kahn Swick & Foti, LLC Investigates Adequacy of Price and Process in Proposed Sale of Esperion Therapeutics, Inc. - ESPRLaw firm Kahn Swick & Foti, LLC has launched an investigation into the proposed acquisition of Esperion Therapeutics, Inc. by funds managed by ARCHIMED, examining whether the offered price of $3.16 per share plus contingent milestone payments adequately compensates shareholders. The firm is seeking shareholders who may wish to discuss their legal rights regarding the transaction. This type of investor alert typically signals that independent counsel is scrutinizing deal terms on behalf of minority shareholders.Stock TitanEsperion reports 6–25% LDL-C cuts in pediatric trialEsperion Therapeutics presented Phase 2 pediatric data at the European Atherosclerosis Society Congress 2026 in Athens showing its drug bempedoic acid reduced LDL cholesterol by 6–25% in children aged 6–17 with heterozygous familial hypercholesterolemia, with similar drug exposure to adults and no new safety concerns. A secondary analysis of the CLEAR Outcomes trial found 42% of statin-intolerant adults achieved at least 30% LDL-C reduction, with greater response associated with female sex, higher baseline LDL-C, and concurrent ezetimibe use. The findings support Phase 3 pediatric studies and expand clinical evidence supporting Esperion's marketed products NEXLETOL and NEXLIZET.