Literature DB >> 31035291

Mavacamten Treatment for Obstructive Hypertrophic Cardiomyopathy: A Clinical Trial.

Stephen B Heitner1, Daniel Jacoby2, Steven J Lester3, Anjali Owens4, Andrew Wang5, David Zhang6, Joseph Lambing6, June Lee6, Marc Semigran6, Amy J Sehnert6.   

Abstract

Background: Mavacamten, an orally administered, small-molecule modulator of cardiac myosin, targets underlying biomechanical abnormalities in obstructive hypertrophic cardiomyopathy (oHCM). Objective: To characterize the effect of mavacamten on left ventricular outflow tract (LVOT) gradient. Design: Open-label, nonrandomized, phase 2 trial. (ClinicalTrials.gov: NCT02842242). Setting: 5 academic centers. Participants: 21 symptomatic patients with oHCM. Intervention: Patients in cohort A received mavacamten, 10 to 20 mg/d, without background medications. Those in cohort B received mavacamten, 2 to 5 mg/d, with β-blockers allowed. Measurements: The primary end point was change in postexercise LVOT gradient at 12 weeks. Secondary end points included changes in peak oxygen consumption (pVO2), resting and Valsalva LVOT gradients, left ventricular ejection fraction (LVEF), and numerical rating scale dyspnea score.
Results: In cohort A, mavacamten reduced mean postexercise LVOT gradient from 103 mm Hg (SD, 50) at baseline to 19 mm Hg (SD, 13) at 12 weeks (mean change, -89.5 mm Hg [95% CI, -138.3 to -40.7 mm Hg]; P = 0.008). Resting LVEF was also reduced (mean change, -15% [CI, -23% to -6%]). Peak VO2 increased by a mean of 3.5 mL/kg/min (CI, 1.2 to 5.9 mL/kg/min). In cohort B, the mean postexercise LVOT gradient decreased from 86 mm Hg (SD, 43) to 64 mm Hg (SD, 26) (mean change, -25.0 mm Hg [CI, -47.1 to -3.0 mm Hg]; P = 0.020), and mean change in resting LVEF was -6% (CI, -10% to -1%). Peak VO2 increased by a mean of 1.7 mL/kg/min (SD, 2.3) (CI, 0.03 to 3.3 mL/kg/min). Dyspnea scores improved in both cohorts. Mavacamten was well tolerated, with mostly mild (80%), moderate (19%), and unrelated (79%) adverse events. The most common adverse events definitely or possibly related to mavacamten were decreased LVEF at higher plasma concentrations and atrial fibrillation. Limitation: Small size; open-label design.
Conclusion: Mavacamten can reduce LVOT obstruction and improve exercise capacity and symptoms in patients with oHCM. Primary Funding Source: MyoKardia.

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Year:  2019        PMID: 31035291     DOI: 10.7326/M18-3016

Source DB:  PubMed          Journal:  Ann Intern Med        ISSN: 0003-4819            Impact factor:   25.391


  37 in total

1.  Actin-binding compounds, previously discovered by FRET-based high-throughput screening, differentially affect skeletal and cardiac muscle.

Authors:  Piyali Guhathakurta; Lien A Phung; Ewa Prochniewicz; Sarah Lichtenberger; Anna Wilson; David D Thomas
Journal:  J Biol Chem       Date:  2020-08-11       Impact factor: 5.157

Review 2.  Hypertrophic Cardiomyopathy: Genetic Testing and Risk Stratification.

Authors:  Fergus Stafford; Kate Thomson; Alexandra Butters; Jodie Ingles
Journal:  Curr Cardiol Rep       Date:  2021-01-12       Impact factor: 2.931

Review 3.  Targeted Medical Therapies for Hypertrophic Cardiomyopathy.

Authors:  Carlo Fumagalli; Maria Grazia De Gregorio; Mattia Zampieri; Elisa Fedele; Alessia Tomberli; Chiara Chiriatti; Alberto Marchi; Iacopo Olivotto
Journal:  Curr Cardiol Rep       Date:  2020-01-28       Impact factor: 2.931

4.  Lessons From MAVERICK-HCM: The Need for Less Speed.

Authors:  Jane E Wilcox; Elizabeth M McNally
Journal:  J Am Coll Cardiol       Date:  2020-06-02       Impact factor: 24.094

5.  Effects of mavacamten on Ca2+ sensitivity of contraction as sarcomere length varied in human myocardium.

Authors:  Peter O Awinda; Yemeserach Bishaw; Marissa Watanabe; Maya A Guglin; Kenneth S Campbell; Bertrand C W Tanner
Journal:  Br J Pharmacol       Date:  2020-10-21       Impact factor: 8.739

Review 6.  Genetic, clinical, molecular, and pathogenic aspects of the South Asian-specific polymorphic MYBPC3Δ25bp variant.

Authors:  Mohammed Arif; Pooneh Nabavizadeh; Taejeong Song; Darshini Desai; Rohit Singh; Sholeh Bazrafshan; Mohit Kumar; Yigang Wang; Richard J Gilbert; Perundurai S Dhandapany; Richard C Becker; Evangelia G Kranias; Sakthivel Sadayappan
Journal:  Biophys Rev       Date:  2020-07-12

7.  Mavacamten preserves length-dependent contractility and improves diastolic function in human engineered heart tissue.

Authors:  Lorenzo R Sewanan; Shi Shen; Stuart G Campbell
Journal:  Am J Physiol Heart Circ Physiol       Date:  2021-01-15       Impact factor: 4.733

8.  Mavacamten decreases maximal force and Ca2+ sensitivity in the N47K-myosin regulatory light chain mouse model of hypertrophic cardiomyopathy.

Authors:  Peter O Awinda; Marissa Watanabe; Yemeserach Bishaw; Anna M Huckabee; Keinan B Agonias; Katarzyna Kazmierczak; Danuta Szczesna-Cordary; Bertrand C W Tanner
Journal:  Am J Physiol Heart Circ Physiol       Date:  2020-12-18       Impact factor: 4.733

9.  Machine Learning for Predicting Heart Failure Progression in Hypertrophic Cardiomyopathy.

Authors:  Ahmed S Fahmy; Ethan J Rowin; Warren J Manning; Martin S Maron; Reza Nezafat
Journal:  Front Cardiovasc Med       Date:  2021-05-13

Review 10.  Pushing the Limits of Medical Management in HCM: A Review of Current Pharmacological Therapy Options.

Authors:  Cristian Stătescu; Ștefana Enachi; Carina Ureche; Laura Țăpoi; Larisa Anghel; Delia Șalaru; Carmen Pleșoianu; Mădălina Bostan; Dragoș Marcu; Mircea Ovanez Balasanian; Radu Andy Sascău
Journal:  Int J Mol Sci       Date:  2021-07-05       Impact factor: 5.923

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