About this trial

The goal of this study is to describe the natural history and clinical events for patients who have Arrhythmogenic Cardiomyopathy with Pathogenic Plakophilin-2 Variants (PKP2-ACM) managed with standard of care.

Eligibility criteria

Qualifiers

None

Disqualifiers

Male or female age 12 years or older at the time of providing informed consent (i.e., ICF provision).

Capable and willing to provide signed informed consent and/or assent, which includes compliance with the requirements and restrictions listed in the ICF and protocol.

Clinical diagnosis of arrhythmogenic cardio myopathy (ACM)

Documentation of a pathogenic or likely pathogenic variant in PKP2 by a CLIA-certified genetic testing laboratory

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

36 Participants
are grouped into 1 trial group

Locations

3
Netherlands
Amsterdam UMC1105 AZ, Amsterdam Netherlands
United States
Boston Children's Hospital02116, BostonMassachusetts, United States
Duke University27710, DurhamNorth Carolina, United States

Sponsors and collaborators

Rocket Pharmaceuticals Inc.

Lead sponsor