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NCT Number: NCT07103655

The Therapeutic Value of Mavacamten in Hypertrophic Cardiomyopathy With Mid-to-Apical Left Ventricular Obstruction

This study is a prospective interventional cohort study aimed at evaluating the therapeutic efficacy and clinical utility of Mavacamten-a targeted myosin inhibitor specifically developed for obstructive hypertrophic cardiomyopathy (HCM)-in patients with HCM characterized by mid-to-apical left ventricular obstruction.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Second Affiliated Hospital, Zhejiang University School of Medicine

Hangzhou, Zhejiang, 310009, China

Location contact

Xiaojie Xie, MD, PhD

CONTACT

[email protected]

571-87784700

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients diagnosed with HCM according to the 2023 Chinese Guidelines for the Diagnosis and Treatment of Adult Hypertrophic Cardiomyopathy, meeting one of the following:
  • Left ventricular wall thickness ≥15 mm at end-diastole in any segment as assessed by echocardiography or cardiac magnetic resonance imaging (CMR);
  • Left ventricular wall thickness ≥13 mm in individuals with a confirmed pathogenic gene mutation or in genetically affected family members;
  • Exclusion of other cardiovascular, systemic, or metabolic disorders that may cause ventricular hypertrophy.
  • Symptomatic non-outflow tract obstructive HCM patients (meeting criterion a and at least one of b or c):

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  • Presence of clinical symptoms such as dyspnea, chest pain, dizziness, palpitations, or syncope, with New York Heart Association (NYHA) functional class II-III;
  • Maximal pressure gradient (PGmax) >30 mmHg in the mid-ventricle under resting or Valsalva maneuver as assessed by echocardiography;
  • PGmax >30 mmHg in the apical region under resting or Valsalva maneuver on echocardiography.

③Ability to provide written informed consent (ICF) and any required privacy authorization prior to study enrollment.

Exclusion criteria

-

  • Obstructive hypertrophic cardiomyopathy (HCM), defined as a maximal left ventricular outflow tract pressure gradient (LVOT-PGmax) ≥30 mmHg at rest and during the Valsalva maneuver on echocardiography;
  • Maximal right ventricular outflow tract pressure gradient (RVOT-PGmax) ≥16 mmHg at rest; ③ Left ventricular ejection fraction (LVEF) <50% on echocardiography;
  • Uncontrolled primary hypertension;
  • Moderate or severe aortic valve stenosis and/or primary mitral valve disease with severe mitral regurgitation; ⑥ Known infiltrative or storage disorders mimicking the HCM phenotype (e.g., Fabry disease, cardiac amyloidosis); ⑦ Presence of severe infections, hepatic dysfunction, renal impairment, or other serious conditions significantly affecting life expectancy.

Treatment and study plan

Mavacamten

Drug

Add Mavacamten to guideline-directed standard medical therapy for patients with hypertrophic cardiomyopathy (HCM) and mid-to-apical left ventricular obstruction.

Other names: beta receptor blockers

Beta Blocker (BB) - metoprolol, bisoprolol, carvedilol

Drug

Administer an appropriate dose of beta-blockers according to the patient's tolerance.

Diltiazem

Drug

Administer an appropriate dose of diltiazem according to the patient's tolerance.

Primary outcomes

  1. Percentage change in pressure gradient during the Valsalva maneuver

    Time frame: Week 36

    The percentage reduction in the pressure gradient at the site of left ventricular obstruction during the Valsalva maneuver at week 36, compared to baseline, as measured by echocardiography.

Secondary outcomes

  1. Anterior papillary muscle to the interventricular septum distance

    Time frame: Week 36

    Percentage Increase in the distance from the anterior papillary muscle to the interventricular septum

  2. Left atrial global longitudinal strain

    Time frame: Week 36

    Left Atrial Global Longitudinal Strain (LA GLS) is an echocardiographic parameter derived from speckle-tracking imaging that measures the longitudinal deformation of the left atrial myocardium throughout the cardiac cycle.

  3. Left ventricular global longitudinal strain

    Time frame: Week 36

    Left Ventricular Global Longitudinal Strain (LVGLS) is a sensitive echocardiographic parameter derived from speckle-tracking imaging that quantifies the myocardial deformation in the longitudinal direction. It reflects the shortening of myocardial fibers along the long axis of the left ventricle during systole.

  4. Percentage change in resting pressure gradient

    Time frame: Week 36

    The percentage reduction in the pressure gradient at the site of left ventricular obstruction at rest measured by echocardiography at week 36 compared to baseline.

  5. Absolute change in pressure gradient during the Valsalva maneuver

    Time frame: Week 36

    The absolute decrease in number of the pressure gradient at the site of left ventricular obstruction during the Valsalva maneuver measured by echocardiography at week 36 compared to baseline.

  6. The proportion of patients with a pressure gradient <30 mmHg during the Valsalva maneuver

    Time frame: Week 36

    The proportion of patients with a pressure gradient <30 mmHg at the site of obstruction during the Valsalva maneuver at week 36.

  7. BNP

    Time frame: Week 36

    Number decrease in BNP levels from baseline to week 36.

  8. Troponin T

    Time frame: Week 36

    Number decrease in Troponin T levels from baseline to week 36.

  9. New-onset atrial fibrillation

    Time frame: From baseline to week 36

    Rate of new-onset atrial fibrillation in each group during the study period

  10. LVEF<50%

    Time frame: From baseline to week 36

    The proportion of patients in each group with LVEF <50% accompanied by signs and symptoms of heart failure worsening and/or an increase in BNP of ≥30% compared to the previous measurement during the study period.

  11. LVEF<40%

    Time frame: From baseline to week 36

    Rate of LVEF <40% in each group during the study period.

Study contacts

Contact information is provided by the study sponsor or research team.

Xiaojie Xie, MD, PhD

CONTACT

[email protected]

571-87784700

Sponsors and collaborators

Lead sponsor

Second Affiliated Hospital, School of Medicine, Zhejiang University

Other

Registry information

Official study title

The Therapeutic Value of Mavacamten in Hypertrophic Cardiomyopathy With Mid-to-Apical Left Ventricular Obstruction: A Prospective, Interventional, Real-World Clinical Study.

Acronym: BRAVE-HCM

Important dates

Study start
2026
Primary completion
2026
Study completion
2027
First posted
Aug 5, 2025
Registry last updated
Jan 21, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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