Author: Ken Dropiewski

Idorsia welcomes Amer Joseph as new Chief Medical Officer and Head of Global Clinical Development

Idorsia thanks Alberto Gimona – most recently Head of Global Clinical Development and Medical Affairs – and wishes him all the best for a well-deserved retirementAmer Joseph joins Idorsia as EVP, Chief Medical Officer & Head of Global Clinical Development, becoming a member of the Idorsia Executive Committee Allschwil, Switzerland – April 9, 2026Idorsia Ltd (SIX: IDIA) announces the appointment of Dr Amer Joseph as Executive Vice President, Chief Medical Officer (CMO) & Head of Global Clinical Development, effective May 1, 2026. He succeeds Dr Alberto Gimona, who is retiring. Amer is an accomplished clinical development leader with a strong track record of delivering regulatory filings, executing mid‑ and late‑stage global clinical development programs, building high‑performing teams, and driving operational excellence with clarity, discipline and speed. His leadership – rooted in scientific rigor, curiosity, and a strong sense of ownership – reflects Idorsia’s culture of innovation, agility, and purposeful execution. As CMO & Head of Global Clinical Development, Amer will lead global clinical strategy and execution across all therapeutic areas, as well as ensure medical governance, helping to advance Idorsia’s pipeline and shape the company’s scientific and medical direction. Jean-Paul Clozel, MD, Chairman and interim CEO of Idorsia commented:“I’m delighted to welcome Amer to Idorsia. His breadth of clinical development experience, passion for advancing science, collaborative leadership style, and energetic, open approach make him an outstanding addition to our organization. Amer brings exactly the vision, discipline, and patient-focused mindset we need as we sharpen our scientific priorities and accelerate progress on our most promising assets. I’m confident he will strengthen our ability to deliver meaningful medicines to patients.” Amer Joseph, MD, commented:“I am truly excited to be joining Idorsia. The company has a remarkable scientific legacy, a strong culture of innovation, and a broad pipeline with real potential to make a difference in the lives of millions of patients. I look forward to working with the leadership team, and the talented teams across the company to advance our medicines with scientific rigor and a deep sense of purpose.” Thanking Alberto GimonaIdorsia extends its heartfelt gratitude to Dr. Alberto Gimona, who retires after years of dedicated service and leadership at Idorsia, most recently as Head of Global Clinical Development and Medical Affairs. Alberto has played a pivotal role in building and guiding Idorsia’s development capabilities and advancing key clinical programs. The company thanks him warmly for his invaluable contributions and wishes him the very best for his retirement. Jean-Paul concluded:“I also want to sincerely thank Alberto for his leadership, dedication, and unwavering commitment to science throughout his years at Idorsia. He has supported our assets and our teams over many years and leaves an amazing legacy of drugs that have made a real difference to so many people over his career. We wish him a very happy and fulfilling retirement.” About Dr Amer JosephAmer joins Idorsia from Chiesi Group, where he most recently served as Vice President, Head of Global Clinical Development, leading a global organization spanning clinical development, clinical operations, biometrics, real-world evidence, and digital health. He delivered late‑stage development programs in respiratory, neonatology, cardiovascular and rare diseases, launched three products in 2023, and drove multiple FDA and EMA approvals. Previously, Amer spent over nine years at Bayer, holding global leadership roles in cardiology and nephrology. He played a pivotal role in developing the blockbuster cardio-renal franchise finerenone, leading Phase 2 and Phase 3 programs involving 13,000 patients across 48 countries and steering global health authority interactions. He also gained rare disease experience at GSK, providing clinical leadership for programs in transthyretin amyloidosis. Amer began his career as a clinician in the United Kingdom, working in leading London hospitals including the London Chest Hospital, St Bartholomew’s, and the Royal London Hospital. He has a deep expertise across the heart-kidney-metabolic axis, strong engagement with global and US key opinion leaders, and considerable experience collaborating with commercial and medical affairs to shape differentiated clinical strategies. He has authored over 40 peer‑reviewed publications in top‑tier journals such as NEJM, JAMA, Circulation, European Heart Journal, and JACC, and has contributed to numerous due diligences and business development processes across rare disease, cardiovascular and renal assets. Notes to the editor About IdorsiaThe purpose of Idorsia is to discover, develop and commercialize innovative medicines to help more patients. To achieve this, we will develop Idorsia into a leading biopharmaceutical company, with a strong scientific core. Headquartered near Basel, Switzerland – a European biotech hub – Idorsia has a highly experienced team of dedicated professionals, covering all disciplines from bench to bedside; QUVIVIQ™ (daridorexant), a different kind of insomnia treatment with the potential to revolutionize this mounting public health concern; strong partners to maximize the value of our portfolio; a promising in-house development pipeline; and a specialized drug discovery engine focused on small-molecule drugs that can change the treatment paradigm for many patients. Idorsia is listed on the SIX Swiss Exchange (ticker symbol: IDIA). For further information, please contact:Investor & Media RelationsIdorsia Pharmaceuticals Ltd, Hegenheimermattweg 91, CH-4123 Allschwil+41 58 844 10 10investor.relations@idorsia.com – media.relations@idorsia.com – www.idorsia.com The above information contains certain “forward-looking statements”, relating to the company’s business, which can be identified by the use of forward-looking terminology such as “intend”, “estimates”, “believes”, “expects”, “may”, “are expected to”, “will”, “will continue”, “should”, “would be”, “seeks”, “pending” or “anticipates” or similar expressions, or by discussions of strategy, plans or intentions. Such statements include descriptions of the company’s investment and research and development programs, business development activities and anticipated expenditures in connection therewith, descriptions of new products expected to be introduced by the company and anticipated customer demand for such products and products in the company’s existing portfolio. Such statements reflect the current views of the company with respect to future events and are subject to certain risks, uncertainties and assumptions. Many factors could cause the actual results, performance or achievements of the company to be materially different from any future results, performances or achievements that may be expressed or implied by such forward-looking statements. Should one or more of these risks or uncertainties materialize, or should underlying assumptions prove incorrect, actual results may vary materially from those described herein as anticipated, believed, estimated or expected.
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First Implant of KingstronBio’s ProStyle M® Transcatheter Mitral Valve System Successfully Completed in National Multicenter Confirmatory Study

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AliveCor Expands AI-Powered 12-lead Cardiac Diagnostics to Vietnam, Advancing Access to Early Detection and Modernized Cardiac Care

Kardia 12L ECG System

Kardia 12L ECG System Enables Faster, Easier Detection of Life-Threatening Cardiac Conditions Using Reduced Leadset

MOUNTAIN VIEW, Calif., April 07, 2026 (GLOBE NEWSWIRE) — AliveCor, the global leader in AI-powered cardiology, today announced the regulatory registration of its Kardia™ 12L electrocardiogram (ECG) System powered by KAI™ 12L AI technology in Vietnam, marking an important step toward expanding AI-enabled cardiac diagnostics across Southeast Asia. The clearance supports Vietnam’s growing commitment to healthcare modernization and strengthens clinicians’ ability to detect and manage cardiovascular disease earlier and more efficiently. Cardiovascular disease remains a leading cause of death globally and across Asia, accounting for 33% of all deaths in Vietnam. Rising rates of hypertension, diabetes, and urbanization-related lifestyle changes are contributing to increasing cardiac risk. At the same time, the Ministry of Health has prioritized digital transformation, hospital capacity optimization, and expanded access to quality care, particularly beyond major urban centers. AI-enabled ECG systems like Kardia 12L align with broader efforts to advance care delivery, support data-driven decision-making, and extend specialist-level insight into frontline settings. Expanding Access to Hospital-Grade Cardiac Insight Kardia 12L is the portable, AI-powered, 12-lead ECG solution whose measurements and ECG interpretation are highly similar to standard 12-lead ECG solutions, right at the point of care, enabling rapid acquisition of complete ECG information and offering a better patient experience. By enabling fast, high-quality diagnostics in clinics, community health centers, and outpatient settings, the platform helps clinicians detect arrhythmias and morphologies including serious conditions like acute myocardial infarction and the most common types of cardiac ischemia earlier, without reliance on traditional, fixed hospital infrastructure. This capability is particularly relevant in Vietnam’s diverse healthcare landscape, where care is delivered across densely populated cities and remote and rural provinces. Kardia 12L supports a more distributed model of cardiac diagnostics, empowering healthcare professionals with accurate, actionable insights wherever patients are seen. Strengthening Healthcare Efficiency and Clinical Confidence Vietnam’s healthcare system continues to manage high patient volumes in major hospitals. Streamlined diagnostic workflows can play a meaningful role in reducing bottlenecks and improving throughput. Kardia 12L’s rapid acquisition and reduced electrode setup simplify the ECG process, shortening preparation time while maintaining diagnostic rigor. The simplified five-electrode setup makes it less invasive for patients, who do not need to fully disrobe during a reading, and typically allows for faster acquisition. Research has shown nearly a 30% reduction in ECG acquisition time compared to standard 12-lead setups. Faster acquisition enables healthcare professionals to move from suspicion to confirmation more quickly, thereby improving triage decisions and accelerating treatment pathways when needed. By combining portability with advanced AI interpretations, the system supports efficient clinician decision making while optimizing patient flow, contributing to both quality and efficiency. Enabling the Next Phase of Digital Cardiac Care As Vietnam advances national digital health initiatives, connected diagnostic tools are becoming increasingly important. Kardia 12L now strengthens AliveCor’s cardiovascular portfolio by standing alongside KardiaMobile and KardiaMobile 6L, creating a unified ecosystem for holistic management of the entire cardiovascular pathway. With its offering expansion into Vietnam, AliveCor reinforces its commitment to supporting healthcare professionals across Southeast Asia with scalable, technology-enabled cardiac solutions designed to improve early detection and expand access to quality cardiovascular care. For more information, sign up for exclusive updates on the Kardia 12L expansion outside of the U.S. here:  https://alivecor.com/uk/forms/kardia-12l-interest-registration. About AliveCorAliveCor, Inc., the leading provider of FDA-cleared personal electrocardiogram (ECG) devices, is transforming cardiology with its medical-grade AI solutions. The company was named to the inaugural TIME World’s Top Health Tech Companies 2025 list – recognition of its commitment to delivering innovative devices and services that empower patients and physicians with personalized, actionable heart data. With over 350 million ECGs recorded, the company’s Kardia devices are the most clinically validated personal ECGs in the world and can remotely detect six of the most common heart arrhythmias in just 30 seconds. The company’s latest offering, Kardia 12L ECG System, powered by KAI 12L cleared to detect 39 cardiac conditions (with determination availability varying by geography), was designed exclusively for use by healthcare providers. AliveCor’s enterprise platform allows third-party providers to manage their patients’ and customers’ heart conditions simply using state-of-the-art tools that provide easy front-end and back-end integration to AliveCor technologies, addressing gaps in care and improving the treatment experience for patients across a range of disease areas. AliveCor is a privately held company headquartered in Mountain View, Calif. For more information, visit alivecor.com and follow us on LinkedIn, X, Instagram and Facebook. Media Contactpress@alivecor.com  Sales ContactOUSenquiries@aliveor.com  A photo accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/7436ab48-0e5f-44b7-9289-6bc166f49740

InterVene Completes First 30 Cases Using the Recana® Thrombectomy Catheter System, Plans for Broader Commercial Launch

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