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. 2025 Jun 23;6(6):CD016183.
doi: 10.1002/14651858.CD016183.

Myosin inhibitors for treatment of hypertrophic cardiomyopathy

Affiliations

Myosin inhibitors for treatment of hypertrophic cardiomyopathy

Samuel Quill et al. Cochrane Database Syst Rev. .

Abstract

This is a protocol for a Cochrane Review (intervention). The objectives are as follows: Primary objective To assess the effects of myosin inhibitors compared to usual care or placebo on exercise capacity, need for septal reduction therapy, and all-cause mortality in people with hypertrophic cardiomyopathy (HCM). Secondary objectives To assess the effects of myosin inhibitors compared to usual care or placebo in people with HCM in the following population subgroups. By demographics, such as age and sex Obstructive HCM versus non-obstructive HCM Genotype-negative and genotype-positive disease People with and without pre-existing atrial fibrillation or other types of arrhythmias.

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Conflict of interest statement

SQ: none.

ASA: has acted as a consultant for Bristol‐Myers Squibb.

FA: has acted as a consultant for Healthsage BV.

CRB: has acted as a consultant for Tenaya Therapeutics, and has received research funding from the Horstingstuit Foundation.

PE: has acted as a consultant for Sarepta Therapeutics Inc, BioMarin Pharmaceutical Inc, Sanofi and Genzyme US Companies, Myokardia, Novo Nordisk, Affinia Therapeutics, Pfizer, Amicus Therapeutics Inc, AstraZeneca, and Bristol‐Myers Squibb. Additionally, PE has participated on a Data And Safety Monitoring for Cytokinetics.

JVD: none.

AFS: none.

Both SQ and AFS confirm that they have no relevant financial interests to declare. They also have not been involved in myosin inhibitor studies. Similarly, neither SQ nor AFS – who are making decisions about study eligibility, data extraction, risk of bias assessment, or GRADE assessments – have been involved in the conduct, analysis, or publication of a study that could be included in the review.

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