Results 151 to 160 of about 1,580 (184)
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New Era: Mavacamten for Obstructive Hypertrophic Cardiomyopathy

Cardiovascular & Hematological Agents in Medicinal Chemistry, 2023
Abstract: Obstructive hypertrophic cardiomyopathy results from asymmetric septal hypertrophy, which eventually obstructs the outflow of the left ventricle. Obstructive hypertrophic cardiomyopathy is linked to mutations in genes that encode for sarcomere proteins, including actin, β-myosin heavy chain, titin, and troponin.
Rami A. Al-Horani, Ma’Lik Woodland
openaire   +2 more sources

Mavacamten (Camzyos)

Canadian Journal of Health Technologies, 2023
CADTH reimbursement reviews are comprehensive assessments of the clinical effectiveness and cost-effectiveness, as well as patient and clinician perspectives, of a drug or drug class. The assessments inform non-binding recommendations that help guide the reimbursement decisions of Canada's federal, provincial, and territorial governments ...
openaire   +1 more source

Evaluation of mavacamten in patients with hypertrophic cardiomyopathy

Journal of Cardiovascular Medicine
Aims We aimed to comprehensively assess the safety and efficacy of mavacamten in hypertrophic cardiomyopathy (HCM) patients. Methods A systematic review and meta-analysis was conducted, and efficacy [changes in postexercise left ventricular outflow tract (LVOT) gradient, left ...
Hui-Ling, Liao, Yi, Liang, Bo, Liang
openaire   +2 more sources

Mavacamten Treatment for Obstructive Hypertrophic Cardiomyopathy

Annals of Internal Medicine, 2019
Mavacamten, an orally administered, small-molecule modulator of cardiac myosin, targets underlying biomechanical abnormalities in obstructive hypertrophic cardiomyopathy (oHCM).To characterize the effect of mavacamten on left ventricular outflow tract (LVOT) gradient.Open-label, nonrandomized, phase 2 trial. (ClinicalTrials.gov: NCT02842242).5 academic
Stephen B, Heitner   +9 more
openaire   +2 more sources

Mavacamten: A Novel Agent for Hypertrophic Cardiomyopathy

Clinical Therapeutics
Hypertrophic cardiomyopathy (HCM) is an under-recognized genetic cardiac disorder affecting the muscles and contractility of the heart, which in turn can result in heart failure symptoms, arrhythmia, and sudden cardiac death. Previously, pharmacotherapy options for HCM were not disease-specific, often poorly tolerated, and overall inadequate for ...
J. Chase Cole   +2 more
openaire   +2 more sources

Mavacamten for obstructive hypertrophic cardiomyopathy

Prescriber
Mavacamten (Camzyos) is a cardiac myosin inhibitor indicated for the treatment of symptomatic obstructive hypertrophic cardiomyopathy. This article discusses its efficacy, adverse effects and place in therapy.
openaire   +1 more source

Mavacamten: treatment aspirations in hypertrophic cardiomyopathy

The Lancet, 2020
Michael, Papadakis   +2 more
openaire   +2 more sources

Efficacy and Safety of Mavacamten in the Treatment of Hypertrophic Cardiomyopathy: A Systematic Review

Heart Lung and Circulation, 2023
Daniel Bishev   +2 more
exaly  

Effect of Chronopharmacology and Food on in Vivo Pharmacokinetic Profile of Mavacamten

Bioanalysis, 2023
Siva Nageswara Rao Gajula   +2 more
exaly  

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