Mavacamten : A Review of a Novel Therapeutic Approach for Hypertrophic Cardiomyopathy

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Hypertrophic Cardiomyopathy (HCM) is a heart disease that can cause left ventricular hypertrophy, arrhythmias, heart failure, and sudden cardiac death. Currently, pharmacological treatment is limited and ineffective. Mavacamten (CamzyosTM) is a cardiac myosin inhibitor developed as a therapeutic option to reduce myocardial contractility and restoration of myocardial function. The Food and Drug Administration (FDA) approved the use of Mavacamten in 2022 for HCM symptoms. Clinical studies have proven that Mavacamten can reduce Left Ventricular Outflow Tract (LVOT) involvement, cardiac hypercontraction, and hypertrophy. This review provides an overview of HCM, its pathophysiology, current treatments, synthesis of Mavacamten, and the clinical trials of Mavacamten.

Medienart:

E-Artikel

Erscheinungsjahr:

2024

Erschienen:

2024

Enthalten in:

Zur Gesamtaufnahme - year:2024

Enthalten in:

Cardiovascular & hematological agents in medicinal chemistry - (2024) vom: 05. Apr.

Sprache:

Englisch

Beteiligte Personen:

Abdul Qadir Memon, Ayesha [VerfasserIn]
Shamim, Areeba [VerfasserIn]
Mirza, Sanoober [VerfasserIn]
Osama, Muhammad [VerfasserIn]
Naeem Muhammad, Iyad [VerfasserIn]
R Wei, Calvin [VerfasserIn]

Links:

Volltext

Themen:

Camzyos
Cardiac myosin inhibitor
Cardiomyopathy
Cardiovascular disease
Clinical studies.
Journal Article
Mavacamten
Novel cardiac drug

Anmerkungen:

Date Revised 08.04.2024

published: Print-Electronic

Citation Status Publisher

doi:

10.2174/0118715257283752240325082733

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM37073940X