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NCT Number: NCT07004972

A Study of Mavacamten in Adults With Obstructive Hypertrophic Cardiomyopathy in India (ROVER)

The purpose of this study is to evaluate the safety, tolerability and effectiveness of mavacamten in adults with obstructive hypertrophic cardiomyopathy in India.

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This study is active but is not currently recruiting participants.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Local Institution - 0014, Hyderabad, Andhra Pradesh, India

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Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Diagnosed with obstructive hypertrophic cardiomyopathy (HCM) consistent with current American College of Cardiology Foundation/American Heart Association and European Society of Cardiology guidelines.
  • Has unexplained LV hypertrophy with nondilated ventricular chambers in the absence of other cardiac (ie, hypertension, aortic stenosis) or systemic disease and with maximal LV wall thickness ≥ 15 mm (or ≥ 13 mm with positive family history of hypertrophic cardiomyopathy).
  • Has LVOT (Valsalva left ventricular outflow tract) peak gradient ≥ 50 mmHg during screening as assessed by TTE at rest or with Valsalva maneuver.
  • Has LVOT peak gradient with Valsalva maneuver at screening TTE of ≥ 30 mmHg.
  • Has adequate acoustic windows to enable accurate TTEs.
  • Has New York Heart Association (NYHA) Class II or III symptoms at screening.
  • Body weight is greater than 45 kg at screening.
  • Documentation of LVEF ≥ 55% at rest of screening TTE.

Exclusion criteria

  • Known infiltrative or storage disorder causing cardiac hypertrophy that mimics obstructive hypertrophic cardiomyopathy, such as Fabry disease, amyloidosis, or Noonan syndrome with LV hypertrophy.
  • Has paroxysmal atrial fibrillation present per the investigator's evaluation of the participant's ECG at the time of screening.
  • Has persistent or permanent atrial fibrillation not on anticoagulation for at least 4 weeks prior to screening and/or not adequately rate controlled within 6 months prior to screening. (Note: Participants with persistent or permanent atrial fibrillation who are anticoagulated and adequately rate-controlled are allowed).
  • Has a history of syncope with exercise within 6 months prior to screening.
  • History of sustained ventricular tachyarrhythmia (> 30 seconds) within 6 months prior to screening.
  • Has documented obstructive coronary artery disease (> 70% stenosis in one or more epicardial coronary arteries) or history of myocardial infarction.
  • Other protocol-defined Inclusion/Exclusion criteria apply.

Treatment and study plan

Mavacamten

Drug

Specified dose on specified days

Other names: BMS-986427

Primary outcomes

  1. Incidence of serious Treatment Emergent Adverse Events (TEAEs)

    Time frame: Up to Week 48

Secondary outcomes

  1. Number of participants with major adverse cardiac events

    Time frame: Up to Week 48

    Major adverse cardiac events includes cardiovascular [CV] death, non-fatal stroke, nonfatal myocardial infarction and hospitalization for heart failure

  2. Number of participants with CV hospitalization

    Time frame: Up to Week 48

  3. Number of participants with heart failure (HF) events

    Time frame: Up to Week 48

    HF includes HF related hospitalizations and urgent emergency room [ER]/outpatient visits

  4. Number of participants with atrial fibrillation/flutter

    Time frame: Up to Weeks 48

  5. Number of participants with syncope

    Time frame: Up to Week 48

  6. Number of participants with left ventricular ejection fraction (LVEF) < 50%

    Time frame: Up to Week 30

  7. Number of participants with left ventricular ejection fraction (LVEF) < 45%

    Time frame: Up to Week 30

  8. Number of participants with left ventricular ejection fraction (LVEF) < 40%

    Time frame: Up to Week 30

  9. Number of participants with left ventricular ejection fraction (LVEF) < 30%

    Time frame: Up to Week 30

  10. Number of participants with non-serious AEs

    Time frame: Up to Week 48

  11. Change from baseline to Week 30 in Valsalva left ventricular outflow tract (LVOT) peak gradient

    Time frame: Up to Week 30

  12. Change from baseline to Week 30 in resting LVOT peak gradient

    Time frame: Up to Week 30

  13. Change from baseline to Week 30 in hs-troponin-I

    Time frame: Up to Week 30

  14. Change from baseline to Week 30 in N-terminal pro b-type natriuretic peptide (NT-proBNP)

    Time frame: Up to Week 30

  15. Proportion of participants with at least 1 class improvement in New York Heart Association (NYHA) functional class from baseline to Week 30

    Time frame: Up to Week 30

    The New York Heart Association (NYHA) functional classification of heart failure assigns participants to 1 of 4 categories based on the participant's symptoms. Heart failure classification will be assessed by the Investigator at specified timepoints in the study. NYHA class at Week 30 will be compared to baseline and the proportion of participants with an improvement of at least one class will be determined.

Sponsors and collaborators

Lead sponsor

Bristol-Myers Squibb

Industry

Registry information

Official study title

A Phase 4, Single-Arm, Open-Label Study to Evaluate Safety, Tolerability, and Efficacy of Mavacamten in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy in India

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Jun 4, 2025
Registry last updated
Apr 28, 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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