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Edgewise Enters HCM Arena | Preventive LAAO September 23, 2024
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Together with
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“It has become increasingly difficult to coerce busy scholars into providing their valuable labor for nothing.”
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Professor Lucina Uddin in a class action lawsuit against the major academic journals.
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A new HCM competitor emerged last week, after Edgewise Therapeutics’ EDG-7500 showed strong evidence of its safety and efficacy in a pair of early-stage trials.
- EDG-7500 is an oral cardiac sarcomere modulator designed to slow early contraction velocity and address impaired cardiac relaxation associated with HCM and other diastolic dysfunctions.
- EDG-7500 is later to the HCM party than BMS’ Camzyos and Cytokinetics’ aficamten, but is differentiated by its potential to improve blood flow without sacrificing LVEF.
Edgewise tested EDG-7500 in a Phase 1 trial to confirm the drug’s side effects, and an early part of a Phase 2 trial to measure EDG-7500’s impact on key oHCM biomarkers – and both trials proved successful.
The Phase 1 trial randomized 48 healthy patients to receive single doses of EDG-7500 or a placebo (5mg – 300 mg), while giving 34 healthy patients ascending doses daily for 14 days (25 to 100 mg), finding that…
- EDG-7500 was well tolerated, with no clinically meaningful changes in vital signs, clinical chemistry, hematology, or electrocardiograms.
- The EDG-7500 groups also had no meaningful changes in LVEF, and none of the subjects experienced a decrease in LVEF <50%.
- Adverse events were similar between the EDG-7500 and placebo groups.
In the CIRRUS-HCM Part A Phase 2 trial, patients with obstructive HCM received single doses of EDG-7500 (50, 100 or 200 mg), finding that…
- Patients taking 100 or 200 mg showed a 67% average reduction in resting LVOT-G and a 55% average reduction in provokable (Valsalva) LVOT-G.
- The 100 mg and 200mg patients also achieved 31% and 64% average reductions in NT-proBNP.
- Gradient reductions were achieved without a meaningful change in LVEF, and EDG-7500 proved to be well tolerated across all doses.
These results support Edgewise’s hypothesis that EDG-7500 can reduce LVOT gradients without reducing LVEF levels, potentially giving it a unique advantage over the current HCM frontrunners.
- Wall Street certainly seemed to agree, driving a 55% surge in Edgewise’s stock price to a three year high of $29.
That added value should come in handy for Edgewise, which is still planning a lot more research on EDG-7500’s safety, efficacy, and treatment dosages for both oHCM and nHCM.
The Takeaway
Edgewise has a long way to go, but this safety and efficacy evidence, and EDG-7500’s potential to reduce LVOT gradients without compromising LVEF could make it a future HCM contender.
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Measuring True Cardiac Risk
How can AI help physicians “see” beyond conventional lipid profiles? Tune in to this on-demand webinar showcasing how Cleerly’s AI-QCT solution complements conventional approaches to evaluating heart disease risk factors, and improves coronary artery disease diagnosis and heart attack risk assessments.
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Cardiology’s Path to Enterprise Imaging
By connecting healthcare teams through every image, every scan and every report, we can reveal the full picture of a patient’s story. Check out this GE HealthCare Cardiology Coffee Break and see how enterprise imaging seamlessly integrates with existing technology infrastructures, ensuring compatibility across systems and platforms, enhances workflow efficiency, and more.
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An All-in-One Coronary Care Solution
See how HeartFlow ONE is transforming precision heart care as the first all-in-one CCTA pathway, combining FFRCT, stenosis, and plaque analysis in a single workflow.
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- EU Recommends Wegovy for HF: Wegovy (semaglutide) might soon be approved in Europe as a heart failure drug, just a few months after the blockbuster GLP-1 gained EU approval for cardiovascular event risk reduction. Based on the positive results from Novo Nordisk’s STEP HFpEF and STEP HFpEF-DM trials, the European Medicines Agency recommended adding HF to Wegovy’s cardiovascular label, while the European Commission will have the final say on this label expansion.
- Preventive LAAO: A JAHA meta-analysis shows that left atrial appendage occlusion (LAAO) may reduce future stroke risk in patients who are undergoing cardiac surgery, even if they don’t have AFib. In six studies (4,130 patients), LAAO cut 5-year stroke rates from 6.8% to 4.3% and improved 4-year survival from 86% to 89.6%, while rates of post-surgery AFib were similar in patients who did and didn’t undergo LAAO.
- Asian Americans’ Mixed MI Care: A large registry study highlighted disparities in Asian Americans’ MI care. Among ~147k adults (3.9% Asian and the rest non-Hispanic white), some Asian male patient groups were far less likely than White men to have door-to-ECG times within 10 minutes (Indian -36%, Chinese -35%, Korean -43%). Korean men were also 35% less likely to get optimal medical therapy, while Indian men were 22% more likely.
- Astellas’ Home HF Solution: Astellas Pharma announced the FDA Class I SaMD listing of its Digitiva heart failure management solution, which combines Eko Health’s digital stethoscope and CVD detection software with Welldoc’s chronic care management capabilities to allow more comprehensive home HF care. Digitiva is Astellas’ first digital health offering in the U.S. and is part of a growing trend of traditional pharma companies expanding into the digital realm (following Bayer, Roche, Pfizer, Novartis, BMS and more).
- ADMIRing PFA’s Paroxysmal AF Impact: Results from the ADMIRE Pivotal Trial show that 75.4% of patients with paroxysmal AFib who were treated with Johnson & Johnson MedTech’s Varipulse PFA platform were free from atrial arrhythmias at 12 months. Among 277 cases, more than 25% of procedures were done without fluoroscopy, with a median procedure time of 81 minutes, and an adverse event rate of just 2.9%.
- PFA for PVCs: Speaking of PFA, could it also be used for ventricular arrhythmias? A small prospective study using the CENTAURI System showed that PFA for PVC ablation achieved acute success and long-term PVC suppression in 85% of cases. Complications were minimal, showing initial promise for PFA as a safe, effective PVC ablation option.
- FH Genetic Screening Alliance: GENinCode, the Family Heart Foundation, and UT Southwestern have teamed up to improve detection of familial hypercholesterolemia. The partners will use GENinCode’s LIPID inCode to identify patients with FH, followed by “cascade screening” to test family members for FH. Testing will be performed at the UT Southwestern Medical Center and VA North Texas Health Care, and after a patient is genetically confirmed to have FH, the Family Heart Foundation will directly contact at-risk family members to educate them and coordinate genetic testing.
- Digital Tools for Heart Failure: Clinicians have a growing array of digital tools for assessing patients with suspected heart failure. A new review article in Lancet Digital Health takes stock of some of the options, noting that many of the tools are based on patient data routinely found in EHRs such as echocardiograms and ECGs, and can help flag high-risk patients.
- COVID’s Toll on Cardiology Staff: A JAHA survey shows the impact that COVID care had cardiology professionals’ wellbeing. In the Coping with COVID survey of 1,199 cardiology healthcare workers in 2020, burnout was reported by 40% of physicians, 59% of nurses, and 57% of other clinical staff. Workload and anxiety/depression were common factors associated with burnout, which caused 23% to 45% to consider quitting, while a sense of being valued helped morale.
- Dapa Delivers with Neuropathy: A post-hoc analysis of the DAPA-HF and DELIVER trials found that diabetic patients with HF and neuropathy might see more benefits from dapagliflozin (Farxiga) than patients who have HF but not neuropathy. Patients with HF and neuropathy from diabetes had a higher risk of worsening HF or cardiovascular death, but Dapagliflozin reduced that risk. Dapagliflozin had a number needed to treat of 9 in patients who had neuropathy, versus 22 in patients who didn’t.
- Journal Publishers in Hot Seat: A class action antitrust lawsuit was filed against the six largest academic journal publishers – Elsevier, Wolters Kluwer, Taylor & Francis Group, John Wiley & Sons, Springer, and Sage – for colluding to profit from scientific research. The litigation reads like the culmination of frustrations that have been coming to a boil for years, alleging the publishers consolidated ownership of 53% of all medical journals while leaving peer-reviewers out to dry and fleecing universities for “the maximum the market will bear for access to that scientific knowledge.”
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AI Algorithms in Cardiology: Navigating the Path from Research to Practice
Join Tempus on Tuesday, September 24 for an in-depth webinar exploring the transformative power of cardiology AI algorithms. Learn from leading experts, including Cedars Sinai’s Dr. David Ouyang and Tempus’ senior cardiology team Dr. Brandon Fornwalt and Dr. John Pfeifer, about how cardiology AI algorithms are unlocking new possibilities for diagnosis, treatment, and patient outcomes. Secure your spot now to be part of this pivotal discussion.
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Bringing AI Into Echo Workflows
Cardiovascular AI solutions are still far more commonly found in cardiology journal papers than in actual clinical workflows, but that’s changing fast and there’s a lot to learn from AI early adopters. Tune into the latest Cardiac Wire Show with Mount Sinai’s Jeffrey Bander, MD and Us2.ai’s Seth Koeppel to see how they launched and expanded their echo AI partnership, and learn how to “adopt echo AI the right way.”
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Addressing Coronary Artery Disease
Learn how the AGENT™ Drug-Coated Balloon provides a new treatment option for in-stent restenosis in the U.S. Rx Only. (Sponsored by Boston Scientific)
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- Merge Cardiology is Best in KLAS: Merge Cardio and Merge Hemo continued their KLAS hot streak, ranking Best in KLAS 2024 for Cardiology and Hemodynamics for the 9th and 12th years. The Merge by Merative cardiology solutions further expanded their KLAS score leads this year, with Merge Cardio scoring 82.8 (up from 82.7 last year) and Merge Hemo surging to 91.5 (from 85.7 in 2023).
- Experience the future of learning: Medtronic Academy 2.0 is here! Unlock your ultimate destination for structural heart medical education with the newly redesigned Medtronic Academy 2.0. Gain access to expert-led courses, webinars, and a wealth of resources to stay ahead in cardiovascular care. Visit now!
- Relieving The Burden of Post-Processing: With the advent of advanced imaging technologies like CCTA come added burdens to technologists and diagnostic imaging centers. See how PIA can relieve the burden of post-processing, saving you time while helping your bottom line.
- How UCSD Improved Post-Stroke Care: Viz Connect improves the monitoring of stroke patients with suspected AFib without adding layers of complexity to the clinical workflow. Hear from Brett C. Meyer, MD, on the impact it has had on post-acute stroke patient care at UCSD.
- Reducing ECG Background Noise: Monebo’s Kinitec Rhythms ECG Algorithm separates true ECG signals from background noise, leading to more accurate diagnoses and improved operator efficiency. See for yourself how the algorithm measured up to a gold standard.
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