Sept. 25, 2025 — Royal Philips has entered a national partnership in the United States with Optum Healthcare. The inclusion of Philips’ Mobile Cardiac Telemetry (MCOT) and Philips Extended Holter (ePatch) in Optum Healthcare's network is designed to enable earlier detection of cardiac conditions and timely clinical intervention.

Sept. 25, 2025 — Kardigan has introduced the three late-stage clinical programs leading its robust pipeline, each strategically chosen to advance the company’s mission of delivering multiple important medicines. These programs target the underlying drivers of specific types of dilated cardiomyopathy (DCM), acute severe hypertension (ASH) and calcific aortic valve stenosis (CAVS), where no treatments exist.

Sept. 24, 2025 — The Family Heart Foundation, a leading research and advocacy organization, has announced the online publication of recommendations from a multidisciplinary panel in the Journal of Pediatrics to promote the early identification of children living with familial hypercholesterolemia (FH). 

Sept. 23, 2025 — Ultromics, a pioneer in AI-driven cardiology solutions, has announced findings from its new study on artificial intelligence (AI) in echocardiography, presented at the American Society of Echocardiography's (ASE) 2025 Scientific Sessions in Nashville, Tennessee. Published as an abstract in the Journal of the American Society of Echocardiography (JASE), the study points to the growing role of AI in helping doctors find cardiac amyloidosis sooner.

Sept. 22, 2025 — Nicklaus Children's Heart Institute in Miami, Florida, is now offering bedside transcatheter patent ductus arteriosus (PDA) closures for medically fragile newborns. This new offering brings advanced therapy directly to the neonatal intensive care unit, allowing procedures to be performed within the baby's own isolette or crib. This eliminates the need to transport the infant to a catheterization laboratory or even outside of their NICU room, removing any risks associated with moving fragile babies.

Sept. 23, 2025 — CeleCor Therapeutics’ multinational Phase 3 clinical trial of its investigational heart-attack drug DisaggproT (zalunfiban) has shown positive primary efficacy and primary safety outcomes. The full results from the CeleBrate study will be released Nov. 10 as part of the late-breaking sessions at the American Heart Association Scientific Sessions in New Orleans.

Sept. 22, 2025 — Heartflow, Inc. has received U.S. Food and Drug Administration (FDA) 510(k) clearance for its Next Gen Heartflow Plaque Analysis algorithm and the platform is now available. The technology features an updated algorithm, vastly expanded nomogram, and advanced 3D color-coded visualization of plaque type, volume and distribution, empowering clinicians with the insights needed to make confident care decisions with ease.

Sept. 22, 2025 — The latest findings on heart failure (HF) published by the Heart Failure Society of America (HFSA) reveal that the lifetime risk of HF has increased to 24%, while the cost of this debilitating condition in the United States continues to soar. According to the HF Stats 2025: Heart Failure Epidemiology and Outcomes Statistics, approximately 6.7 million Americans over 20 years of age have HF, and the prevalence is expected to rise to 8.7 million by 2030.

Sept. 18, 2025 — BioCardia, Inc., a developer of cellular and cell-derived therapeutics for treating cardiovascular and pulmonary diseases, has announced the primary endpoint results of the open label roll-in cohort of the CardiAMP Cell Therapy in Chronic Myocardial Ischemia Trial.

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