Results 101 to 110 of about 385 (131)
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Aficamten—A Second in Class Cardiac Myosin Inhibitor for Hypertrophic Cardiomyopathy
Cardiology in Review, 2023Hypertrophic cardiomyopathy is an under-recognized disease with a genetic component that results in abnormal and often asymmetric thickening of the left ventricle in addition to decreased compliance and progressive fibrosis of the myocardium. It further poses significant complications related to dynamic left ventricular outflow obstruction over time in
Jay, Patel +4 more
openaire +2 more sources
Effect of Aficamten on Health Status Outcomes in Obstructive Hypertrophic Cardiomyopathy
Background: A primary goal in treating obstructive hypertrophic cardiomyopathy (oHCM) is to improve patients’ health status: their symptoms, function, and quality of life. The health status benefits of aficamten, a novel cardiac myosin inhibitor, have not been comprehensively described. Objectives: This study sought to determine the effect of aficamten
Michael Nassif, Pablo García-Pavía
exaly +3 more sources
Innovative pharmacological approaches to hypertrophic cardiomyopathy: The emerging role of Aficamten
Current Problems in CardiologyHypertrophic cardiomyopathy (HCM) is a genetic cardiac disorder characterized by left ventricular hypertrophy (LVH), which can lead to left ventricular outflow tract (LVOT) obstruction. Traditional treatments often provide limited symptom relief and may not adequately reduce the LVOT gradient.
Adetola Emmanuel Babalola +2 more
exaly +3 more sources
Aficamten in Non-Obstructive Hypertrophic Cardiomyopathy: Unlocking New Horizons?
European Journal of Heart FailureN ...
Rossi, Maddalena +2 more
openaire +3 more sources
Aficamten (Myqorzo) for Obstructive Hypertrophic Cardiomyopathy
The Medical Letter on Drugs and TherapeuticsAficamten (Myqorzo – Cytokinetics), an oral cardiac myosin inhibitor, has been approved by the FDA to improve functional capacity and symptoms in adults with symptomatic obstructive hypertrophic cardiomyopathy (HCM). It is the second cardiac myosin inhibitor to be approved in the US for this indication; mavacamten (Camzyos) was approved in 2022.
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The American Journal of Cardiology
Myosin inhibitors represent a novel therapeutic class for hypertrophic cardiomyopathy (HCM). While both mavacamten and aficamten have been evaluated in randomized trials, comparative evidence across the 2 agents remains limited. We performed a systematic review and meta-analysis of 8 randomized controlled trials of myosin inhibitors in HCM.
Md Fahim +7 more
openaire +2 more sources
Myosin inhibitors represent a novel therapeutic class for hypertrophic cardiomyopathy (HCM). While both mavacamten and aficamten have been evaluated in randomized trials, comparative evidence across the 2 agents remains limited. We performed a systematic review and meta-analysis of 8 randomized controlled trials of myosin inhibitors in HCM.
Md Fahim +7 more
openaire +2 more sources
Aficamten for Obstructive Hypertrophic Cardiomyopathy
New England Journal of MedicineJorge, Pedreira-Bouzas +2 more
openaire +3 more sources
Aficamten Monotherapy for Hypertrophic Cardiomyopathy
New England Journal of MedicineMapelli, Massimo +2 more
openaire +4 more sources
A Phase 1 Dose-Escalation Study of the Cardiac Myosin Inhibitor Aficamten in Healthy Participants
JACC Basic To Translational Science, 2022Fady Malik +2 more
exaly

