Daiichi Sankyo Europe Reaffirms Commitment to Patient-Centred Care with Extensive Data Showcase at EAS Congress 2026
26.5.2026 17:00:00 CEST | Business Wire | Press Release
Daiichi Sankyo Europe (DSE) is pleased to announce its extensive scientific presence at the European Atherosclerosis Society (EAS) Congress 2026. The presentation of 15 abstracts, comprising both clinical trial analyses and real-world evidence, underscores the company's sustained investment in cardiovascular health and its mission to care for every heartbeat.
The 15-abstract showcase provides a comprehensive look at the role of bempedoic acid in lipid management. This includes post-hoc analyses in collaboration with Esperion Therapeutics from the Phase 3 CLEAR Outcomes trial exploring its impact on stroke and venous thromboembolism (VTE) incidence.5,6 There are also real-world findings from the MILOS registry, including a dedicated sub-analysis investigating the effectiveness of bempedoic acid across various background therapies.1,2,3,4 Results reinforce consistent effectiveness and safety profile of bempedoic acid across various EU countries and regardless of patients’ existing treatment regimens.7
DSE’s commitment to expanding the evidence base for bempedoic acid is further reflected in new Esperion sponsored data being presented in paediatric patients (aged 6–17 years old) with familial hypercholesterolemia.8 Alongside the recent label update regarding breastfeeding – where use may now be considered by weighing the benefit of therapy for the mother against the child’s benefit from breastfeeding – these milestones underscore DSE’s ongoing efforts to study bempedoic acid across all populations, including specific underserved groups, to ensure as many patients as possible can achieve their LDL-C goals.9,10
"Far too many patients across Europe still fail to reach their LDL-C targets, leaving them unnecessarily exposed to cardiovascular risk," says Prof. Maurizio Averna, Professor of Internal Medicine, School of Medicine, University of Palermo, Italy. "The real-world data being presented at EAS 2026 provide critical evidence to help clinicians bridge these treatment gaps in routine practice and improve outcomes for a diverse range of patients."
"At Daiichi Sankyo Europe, our commitment goes beyond clinical data; it is rooted in the individual journey of every patient," said Dr. Stefan Seyfried, Vice President and Head of Medical Affairs, Specialty Medicines, Daiichi Sankyo Europe."The extensive data set we are presenting at EAS 2026 – a testament to our sustained investment in cardiovascular health – reinforces our mission to give every patient a chance to reach their treatment goals. By translating scientific innovation into practical, patient-centred care, we are ensuring that we care for every heartbeat through innovative and accessible solutions."
By emphasizing bempedoic acid’s ability to deliver improved cardiovascular outcomes and low-density lipoprotein cholesterol (LDL-C) reduction, irrespective of background therapy and patient subgroup, DSE aims to ensure that healthcare professionals have the evidence needed to support their lipid management treatment decisions.
Data Being Presented at EAS Congress 2026
MILOSstudy
Presentation title | Author | Session (Time, EEST) |
UK Real-World Experience with Bempedoic Acid in Dyslipidaemia: 1-Year Results from the MILOS Study | K. K. Ray | Oral 25 May 14:56-15:03 |
Real-world effectiveness and safety of bempedoic acid: Insights from the 1-year follow-up Italian cohort data of the MILOS study | M. Averna | Oral 25 May 14:56-15:03 |
Effectiveness and safety of bempedoic acid in routine clinical practice: 1-year follow-up data from MILOS Belgian cohort | T. Vanassche | Oral 26 May At all times |
Real-World One-Year Data on the Use of Bempedoic Acid in Patients with Dyslipidemia: Insights from the MILOS Austria Study | T. Stulnig | Poster Discussion 25 May 14:49-14:56 |
Real-World Use of Bempedoic Acid in Spain: 8-Week Results from the MILOS Study | J.J. Gómez Doblas | Virtual Poster At all times |
Swiss Real-World Experience with Bempedoic Acid in Dyslipidaemia: 8-Week Results from the Observational, Prospective MILOS Study | K. Koskinas | Poster on Board 24-25 May At all times |
Comparable LDL-C reductions with bempedoic acid used alone or with background statin and/or ezetimibe therapy: real world evidence from the MILOS study | T. Vanassche | Oral 26 May 16:45-17:00 |
CLEAR Outcomes trial
Presentation title | Author | Session (Time, CET) |
Factors associated with enhanced LDL cholesterol lowering with bempedoic acid among statin-intolerant patients from CLEAR Outcomes (in collaboration with Esperion Therapeutics) | C. M. Ballantyne | Oral Presentation 25 May 15:03-15:10 |
The association between bempedoic acid and risk of venous thromboembolism: A post hoc analysis of the CLEAR Outcomes trial (in collaboration with Esperion Therapeutics) | S. J. Nicholls | Oral Presentation 25 May 11:30-11:40 |
Bempedoic acid and incidence of stroke among statin-intolerant patients: An analysis of the CLEAR Outcomes trial (in collaboration with Esperion Therapeutics) | S. J. Nicholls | Oral Presentation 26 May 13:44-13:51 |
Bempedoic acid without background LLT, LDL cholesterol and cardiovascular events: a secondary analysis of the CLEAR Outcomes trial | K. K. Ray | Science at a Glance 26 May 13:51-13:58 |
CLEAR Path 1 trial
Presentation title | Author | Session (Time, EEST) |
Bempedoic acid in children aged 6-17 years with heterozygous familial hypercholesterolemia: a Phase 2 study (Esperion Therapeutics-sponsored) | S. Gidding | Science at a Glance 25 May 14:35-14:42 |
About MILOS
MILOS (NCT04579367) is an ongoing, multinational, European observational study in adult patients diagnosed with primary hypercholesterolaemia or mixed dyslipidaemia.11 The aim is to evaluate the real-world use of bempedoic acid and bempedoic plus ezetimibe fixed-dose combination. Beyond Germany, MILOS has sites in Austria, Belgium, Italy, the Netherlands, Spain, Switzerland and the UK.11
About CLEAR Outcomes trial
The CLEAR Outcomes trial was a double‑blind, randomized, placebo‑controlled study designed to evaluate the effect of bempedoic acid on cardiovascular (CV) outcomes in statin‑intolerant patients for whom primary or secondary CV prevention was clinically indicated.12 The trial enrolled 13,970 patients aged 18–85 years (mean age 65.5 years), nearly half of whom were women, all of whom had established or were at high risk for cardiovascular disease and a mean baseline LDL‑C of 139 mg/dL (3.59 mmol/L).12 Conducted at 1,250 sites across 32 countries, patients were randomized to receive oral bempedoic acid 180 mg daily or placebo and were followed for a median of 40.6 months.12 The primary endpoint was a four‑component composite of major adverse cardiovascular events (MACE‑4): CV death, non‑fatal myocardial infarction, non‑fatal stroke, or coronary revascularization, with multiple key secondary CV endpoints also assessed.12
About Daiichi Sankyo
Daiichi Sankyo (TSE: 4568) is a global healthcare company committed to becoming a trusted healthcare innovator, transforming the lives of people through its strength in science and technology. The company discovers and develops new standards of care to address diverse medical needs to fulfill its purpose of contributing to the enrichment of quality of life around the world. With a strategic focus on oncology, Daiichi Sankyo is advancing an industry-leading antibody drug conjugate portfolio along with identifying new breakthrough generating technologies to deliver practice-changing medicines to patients, healthcare professionals and society. For more information, please visit www.daiichisankyo.com.
References
- Averna M, et al. Real-world effectiveness and safety of bempedoic acid: Insights from the 1-year follow-up Italian cohort data of the MILOS study. Presented at European Atherosclerosis Society (EAS) Congress 2026.
- Ray KK, et al. UK Real-World Experience with Bempedoic Acid in Dyslipidaemia: 1-Year Results from the MILOS Study. Presented at European Atherosclerosis Society (EAS) Congress 2026.
- Stulnig T, et al. Real-World One-Year Data on the Use of Bempedoic Acid in Patients with Dyslipidemia: Insights from the MILOS Austria Study. Presented at European Atherosclerosis Society (EAS) Congress 2026.
- Vanassche T, et al. Effectiveness and safety of bempedoic acid in routine clinical practice: 1-year follow-up data from MILOS Belgian cohort. Presented at European Atherosclerosis Society (EAS) Congress 2026.
- Nicholls SJ, et al. Bempedoic acid and incidence of stroke among statin-intolerant patients: An analysis of the CLEAR Outcomes trial. Presented at European Atherosclerosis Society (EAS) Congress 2026.
- Nicholls SJ, et al. The association between bempedoic acid and risk of venous thromboembolism: A post hoc analysis of the CLEAR Outcomes trial. Presented at European Atherosclerosis Society (EAS) Congress 2026.
- Ray KK, et al. Bempedoic acid without background LLT, LDL cholesterol and cardiovascular events: a secondary analysis of the CLEAR Outcomes trial. Presented at European Atherosclerosis Society (EAS) Congress 2026.
- Gidding SS, et al. Bempedoic Acid in Children aged 6-17 years with Heterozygous Familial Hypercholesterolaemia: A Phase 2 Study. Presented at European Atherosclerosis Society (EAS) Congress 2026.
- European Medicines Agency. Nilemdo – summary of product characteristics (SmPC). Available at: https://www.ema.europa.eu/en/documents/product-information/nilemdo-epar-product-information_en.pdf. Last accessed May 2026.
- European Medicines Agency. Nustendi – summary of product characteristics (SmPC). Available at: https://www.ema.europa.eu/en/documents/product-information/nustendi-epar-product-information_en.pdf. Last accessed May 2026.
- Treatment with bempedoic acid and/or its fixed-dose combination with ezetimibe in primary hypercholesterolemia or mixed dyslipidemia (MILOS). Available at: https://clinicaltrials.gov/study/NCT04579367?viewType=Card&term=NCT04579367&rank=1. Last accessed April 2026.
- Nissen SE, et al. Bempedoic Acid and Cardiovascular Outcomes in Statin-Intolerant Patients. N Engl J Med. 2023. 13;388(15):1353-1364.
- Ballantyne CM, et al. Factors associated with enhanced LDL cholesterol lowering with bempedoic acid among statin-intolerant patients from CLEAR Outcomes. Presented at European Atherosclerosis Society (EAS) Congress 2026.
- J.J. Gómez Doblas, et al. Real-World Use of Bempedoic Acid in Spain: 8-Week Results from the MILOS Study. Presented at European Atherosclerosis Society (EAS) Congress 2026.
- K. Koskinas, et al. Swiss Real-World Experience with Bempedoic Acid in Dyslipidaemia: 8-Week Results from the Observational, Prospective MILOS Study. Presented at European Atherosclerosis Society (EAS) Congress 2026.
- Vanassche T, et al. Comparable LDL-C reductions with bempedoic acid used alone or with background statin and/or ezetimibe therapy: real world evidence from the MILOS study. Presented at European Atherosclerosis Society (EAS) Congress 2026.
View source version on businesswire.com: https://www.businesswire.com/news/home/20260526953274/en/
Contacts
Media Contact
Shreya Pandey
Daiichi Sankyo Europe GmbH
Senior Public Relations Manager
+49 151 54478370
(c) 2024 Business Wire, Inc., All rights reserved.
Business Wire, a Berkshire Hathaway company, is the global leader in multiplatform press release distribution.
Subscribe to releases from Business Wire
Subscribe to all the latest releases from Business Wire by registering your e-mail address below. You can unsubscribe at any time.
Latest releases from Business Wire
SLB Announces Date for Second-Quarter 2026 Results Conference Call26.5.2026 19:00:00 CEST | Press Release
SLB (NYSE: SLB) will hold a conference call on July 24, 2026, to discuss the results for the second quarter ending June 30, 2026. The conference call is scheduled to begin at 9:30 a.m. U.S. Eastern time and a press release regarding the results will be issued at 7:00 a.m. U.S. Eastern time. To access the conference call, listeners should contact the Conference Call Operator at +1 (800) 715-9871 within North America or +1 (646) 307-1963 outside of North America approximately 10 minutes prior to the start of the call and the access code is 3440360. A webcast of the conference call will be broadcast simultaneously at https://events.q4inc.com/attendee/157027565 on a listen-only basis. Listeners should log in 15 minutes prior to the start of the call to test their browsers and register for the webcast. Following the end of the conference call, a replay will be available at www.slb.com/irwebcast until July 31, 2026, and can be accessed by dialing +1 (800) 770-2030 within North America or +1
Alipay Launches Next-Generation AI Payment Infrastructure, Debuts AI Wallet and Token Pay to Power Agentic Economy26.5.2026 17:20:00 CEST | Press Release
Alipay today introduced its full-stack AI payment solution to partners across industries, ranging from AI companies to traditional retailers, and debuted two new services — the world’s first AI Wallet and Token Pay — to support the agentic economy’s rapid growth. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260526337824/en/ Alipay Unveils Next-generation AI Payment Infrastructure This launch extends Alipay's next-generation AI payment infrastructure, building on its consumer-facing product Alipay AI Pay and its business-facing AI payment processing product. “While the essence of commerce remains unchanged in the age of AI, the emergence of AI agents is reshaping everything. Drawing on 22 years of technological expertise and commercial know-how, Alipay is building a new generation of AI payment services to accelerate the growth of the agentic commerce ecosystem,” said Cyril Han, CEO of Ant Group. AI Wallet: Giving Users Vis
OpenRouter Raises $113 Million CapitalG-led Series B as Weekly Volume Explodes to 25T Tokens26.5.2026 15:15:00 CEST | Press Release
OpenRouter, the AI model exchange, today announced a $113 million Series B led by Alphabet’s independent growth fund, CapitalG, with participation from investors including NVentures (NVIDIA’s venture capital arm), ServiceNow Ventures, MongoDB Ventures, Snowflake Ventures, Databricks Ventures, alongside existing investors including Andreessen Horowitz and Menlo Ventures. OpenRouter’s volume has surged to 25 trillion tokens per week (100 trillion tokens per month), representing a 5X increase from the 5 trillion tokens processed per week just six months ago. The explosion in token demand illustrates how quickly enterprises are deploying agents and scaling AI across multiple models and providers. OpenRouter’s infrastructure manages and optimizes inference and provides access to 400+ models across leading AI providers, including Anthropic, Google, OpenAI, xAI, and DeepSeek, among others. The platform is used by over 8 million global users, including AI-native startups and large enterprises,
Xsolla Expands Its Community Management Tools for Creators, Community Leaders, and Resellers26.5.2026 15:00:00 CEST | Press Release
Xsolla, a leading global video game commerce company, today announced three simultaneous expansions of its community management tools and products. As the creator economy continues to reshape how games are discovered and the industry accelerates its shift toward direct-to-consumer commerce, Xsolla is building on its community management tools for creators, community leaders, and emerging markets, and will showcase them at TwitchCon Rotterdam later this month. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260526596720/en/ Graphic: Xsolla The games industry has never had a shortage of people who drive player acquisition, loyalty, and commerce; it's had a shortage of infrastructure that recognizes them. Creators stream it. Community leaders build a culture around it. Local resellers get it into the hands of players in markets traditional channels can't reach. Each operates at the center of how games are discovered, adopted, an
Biocytogen Launches AI-Powered RenSuper™ Platform and Industry-First Fully Automated Antibody Discovery Infrastructure26.5.2026 14:00:00 CEST | Press Release
Biocytogen today announced the launch of RenSuper Workstation, a next-generation AI-powered antibody discovery platform providing off-the-shelf access to a large-scale, experimentally validated library of fully human therapeutic antibody sequences, together with the RenSuper High-Throughput Antibody Manufacturing Automation Center, a fully automated infrastructure designed to accelerate antibody validation and production. Built on Biocytogen’s proprietary RenMice® platforms, RenSuper establishes a closed-loop antibody discovery engine combining in vivo immune repertoires, AI-driven candidate selection, automated experimental validation, and scalable manufacturing infrastructure. The platform supports the discovery and development of monoclonal antibodies, bispecifics, multispecifics, antibody-drug conjugates (ADCs), VHHs, and other advanced therapeutic modalities, significantly reducing the time and risk associated with antibody discovery. RenSuper Workstation: AI-Powered One-Click Tar
In our pressroom you can read all our latest releases, find our press contacts, images, documents and other relevant information about us.
Visit our pressroom