Cardiomyopathy Trial, Recruiting NCT07557498 Sponsor: Bristol-Myers Squibb Condition: Cardiomyopathy
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Cardiomyopathy Trial, Recruiting

NCT07557498
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • Adults aged 18 or older at the time the study begins looking at their records
  • People who have been formally diagnosed with obstructive hypertrophic cardiomyopathy (a condition where the heart muscle becomes abnormally thick, blocking blood flow)
  • People who were prescribed a medication called mavacamten for this heart condition at one of the study sites, between 28 April 2022 and 31 December 2024
  • People who have never been enrolled in an interventional clinical trial (a trial testing a treatment) involving a type of heart medication called a cardiac myosin inhibitor — though having taken part in observational studies (where researchers only observe, not treat) is allowed
  • People who were not enrolled in any interventional clinical trial at the time the study begins reviewing their records
  • For the survey part of the study only: people who are also able to read and understand English and have access to a computer or smartphone to complete an online survey

Who may not be able to join:

  • There are no specific exclusion criteria listed beyond not meeting all of the inclusion criteria above

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 21 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Bristol-Myers Squibb, Bristol-Myers Squibb

Phone: 855-907-3286

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
15 January 2026
Est. completion
14 December 2026

Where this trial is recruiting

🇬🇧 United Kingdom

Primary endpoints

Participant blood pressure (both systolic and diastolic); Date of diagnosis of hypertrophic cardiomyopathy; Hypertrophic cardiomyopathy genetic testing results; Family history of hypertrophic cardiomyopathy; Family history of Sudden Cardiac Death (SCD); Participant comorbidities (cardiovascular and non-cardiovascular ); Type of prior surgeries and procedures; Participant New York Heart Association (NYHA) class category; Change in participant New York Heart Association (NYHA) class from baseline; Duration of mavacamten treatment; Number of mavacamten dose titrations; Type of mavacamten dose tri...

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov