Press Releases May 13, 2026 08:00 AM

Esperion Announces Two New Analyses Supporting Bempedoic Acid to Reduce LDL-C Levels to be Presented at the European Atherosclerosis Society (EAS) Congress 2026

Esperion Announces New Data Supporting Bempedoic Acid's LDL-C Lowering Benefits in Pediatric and Adult Patients

By Jordan Park ESPR

Esperion Therapeutics announced the presentation of new analyses at the European Atherosclerosis Society Congress 2026. The data highlights the efficacy of bempedoic acid in lowering LDL cholesterol in children with heterozygous familial hypercholesterolemia as well as factors enhancing LDL-C reduction in adults. These findings support advancing bempedoic acid into Phase 3 pediatric trials and provide insights for optimizing clinical use, underscoring the drug's potential to reduce cardiovascular risk in both pediatric and adult populations.

Esperion Announces Two New Analyses Supporting Bempedoic Acid to Reduce LDL-C Levels to be Presented at the European Atherosclerosis Society (EAS) Congress 2026
ESPR

Key Points

  • Phase 2 pediatric study shows bempedoic acid effectively reduces LDL-C in children with heterozygous familial hypercholesterolemia.
  • New CLEAR Outcomes trial analyses identify patient factors linked to greater LDL-C reductions among statin-intolerant adults.
  • Multiple abstracts including post hoc analyses of cardiovascular outcomes will be presented, reinforcing bempedoic acid's role in lipid-lowering therapy.
  • Impacted sectors include pharmaceuticals, healthcare, and cardiovascular therapeutics markets.

– Presentations Examine Findings From the Pediatric Phase 2 Study, As Well As Factors Associated With Enhanced LDL-C Reductions in Adult Patients Enrolled in Clear Outcomes

Pediatric Phase 2 Study Demonstrated Bempedoic Acid Treatment Reduced LDL-C in Children with Heterozygous Familial Hypercholesterolemia (HeFH) Congruent with Reductions in Adult Exposures

New Analyses from CLEAR Outcomes Trial Identified Factors Associated With Enhanced LDL-C Reductions in Adult Patients

ANN ARBOR, Mich., May 13, 2026 (GLOBE NEWSWIRE) -- Esperion (NASDAQ: ESPR) today announced that two new abstracts and three encore abstracts have been accepted for presentation at the European Atherosclerosis Society (EAS) Congress 2026 taking place on May 24-27, 2026, in Athens, Greece.

“We are pleased to present supportive new data to the global lipid community at EAS Congress 2026, as they highlight the breadth and durability of our bempedoic acid products to meaningfully lower LDL-C levels and reduce the risk of cardiovascular events,” said Sheldon Koenig, President and CEO of Esperion. “Results from our Phase 2 pediatric study demonstrate LDL C reductions in children with heterozygous familial hypercholesterolemia are consistent with those observed in adults, supporting the advancement of bempedoic acid into Phase 3 development for pediatric patients with HeFH and homozygous familial hypercholesterolemia. These findings represent an important step toward expanding treatment options for patients with lifelong cardiovascular risk.

“In collaboration with our partner, Daiichi Sankyo Europe, we are also presenting a new analysis from the CLEAR Outcomes trial that identifies patient characteristics associated with achieving robust LDL C reductions of 30% or greater, providing additional insight into how bempedoic acid can be optimally utilized in clinical practice,” added Koenig.

Original Research

Abstract Title:   

Abstract #:         
Location:        
Date & Time:             
Session Title:
Presenter: Bempedoic Acid In Children Aged 6-17 Years With Heterozygous
Familial Hypercholesterolaemia: A Phase 2 Study
178
Station 08
May 25, 2026; 7:35-8:35 AM EST
Science-at-a-Glance (SaaG) Session: Real-World Lipid-Lowering Therapies and Determinants of Treatment Success
Samuel S Gidding, MD  Abstract Title: 


Abstract #:         
Location:        
Date & Time:
Session Title:
Presenter:         Factors Associated With Enhanced LDL-Cholesterol Lowering With
Bempedoic Acid Among Statin-Intolerant Patients From CLEAR
Outcomes
338
Station 08
May 25, 2026; 7:35-8:35 AM EST
SaaG Session: Real-World Lipid-Lowering Therapies and Determinants of Treatment Success
Christie M Ballantyne, MD

Encore Presentations

Abstract Title:   
Session ID:                 
Location:
Date & Time:          
Session Title:
Presenter:         The Association Between Bempedoic Acid And Risk Of Venous Thromboembolism: A Post Hoc Analysis Of The CLEAR Outcomes Trial
122
Elisaf Hall
May 25, 2026; 3:30-5:00 AM EST
New perspectives on lipid lowering therapies
Prof. Stephen J Nicholls, MBBS, PhD
  Abstract Title:   

Abstract #:                 
Location
Date & Time:             
Session Title:
Presenter:         Bempedoic Acid And Incidence Of Stroke Among Statin-
Intolerant Patients: An Analysis Of The CLEAR Outcomes Trial
481
Station 07
May 25, 2026; 6:30-7:30 AM EST
SaaG Session: Novel Lipid-Lowering Therapies: Clinical Outcomes and Real-World Evidence
Prof. Stephen J Nicholls, MBBS, PhD
  Abstract Title:   

Abstract #:                 
Location
Date & Time:             
Session Title:
Presenter:         Bempedoic Acid Without Background LLT, LDL Cholesterol And Cardiovascular Events: A Secondary Analysis Of The CLEAR Outcomes Trial
455
Station 07
May 25, 2026; 6:30-7:30 AM EST
SaaG Session: Novel Lipid-Lowering Therapies: Clinical Outcomes and Real-World Evidence
Prof. Kausik K Ray, MD

Esperion Therapeutics
Esperion Therapeutics, Inc. is a commercial-stage biopharmaceutical company dedicated to developing and delivering innovative cardiometabolic and rare/orphan disease therapies. The Company leverages deep domain expertise in ACLY biology to develop and commercialize transformative medicines for patients worldwide. Esperion currently markets two oral, once-daily, non-statin therapies for patients struggling to maintain their low-density lipoprotein cholesterol (LDL-C) levels and are at risk of cardiovascular disease.

With a broad U.S. commercial infrastructure and global approvals across more than 40 countries, Esperion is well positioned to serve as a partner-of-choice for global innovators seeking U.S. market access through acquisition, in-license, co-promotion and revenue share opportunities. In tandem, the Company is advancing its leadership in ACLY biology to build a diversified pipeline of novel product candidates, including treatments for Primary Sclerosing Cholangitis and renal diseases. For more information, visit esperion.com and follow Esperion on LinkedIn and X.

Esperion Contact Information:
Investors:
Alina Venezia
[email protected]
(734) 887-3903

Media:
Tiffany Aldrich
[email protected]
(616) 443-8438


Risks

  • Advancement to Phase 3 pediatric trials depends on continued positive safety and efficacy data.
  • Market adoption may be limited if statin-intolerant patient subsets do not respond as expected.
  • Competitive landscape in cardiovascular and lipid-lowering therapies remains intense, potentially impacting commercial success.

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