Cardiomyopathy Trial, Recruiting NCT06644742 Sponsor: Rocket Pharmaceuticals Inc. Condition: Cardiomyopathy
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Cardiomyopathy Trial, Recruiting

NCT06644742
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:

  • You are 12 years old or older at the time of signing the consent form
  • You are able and willing to sign a consent form and follow the study's rules and requirements
  • You have been diagnosed with a heart condition called arrhythmogenic cardiomyopathy (ACM), a disease affecting the heart muscle and its rhythm
  • Genetic testing done by an approved laboratory has found a specific harmful change (variant) in a gene called PKP2 linked to your condition
  • You had a defibrillator (ICD) implanted at least 6 months before joining the study
  • A heart scan (echocardiogram or MRI) done within the past 12 months shows your heart's pumping function (left ventricular ejection fraction) is at 50% or above

Who may not be able to join:

  • Your genetic test results suggest your heart condition may be caused by a gene change other than a specific type of PKP2 variant
  • You are currently taking part in another clinical trial using an experimental treatment that could affect this study's results
  • You have previously taken part in a study involving gene therapy or gene editing
  • You have very severe heart failure (known as NYHA Class IV), meaning you have symptoms even at rest
  • You currently need, or are expected to need within 6 months, a mechanical device to help your heart pump, or a heart transplant
  • You have previously had a heart transplant or transplant of another major organ (such as lungs or liver)
  • Your heart has been found within the past 12 months to rely entirely on a pacemaker to beat
  • You have tested positive for HIV
  • You are unwilling or unable to follow the study's procedures, attend follow-up appointments, or cooperate fully with the research team

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 26 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

Phone: 646-627-0033

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
Sponsor
Rocket Pharmaceuticals Inc.
Registry
ClinicalTrials.gov
Start date
1 March 2026
Est. completion
1 December 2030

Where this trial is recruiting

🇳🇱 Netherlands 🇺🇸 United States

Primary endpoints

Heart rhythm and rate monitoring measures; Cardiac biomarkers

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: 26 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