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arrhythmogenic right ventricular cardiomyopathy (ARVC) - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

arrhythmogenic right ventricular cardiomyopathy

MONDO:0016587

Also known as:ARVCARVC cardiomyopathyARVD

Find Clinical TrialsTrials

Overview

Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heart muscle disease that consists in progressive dystrophy of primarily the right ventricular myocardium with fibro-fatty replacement and ventricular dilation, and that is clinically characterized by ventricular arrhythmias and a risk of sudden cardiac death.

OnsetCONGENITAL

Clinical Trials18 registered · 13 recruiting

Diagnosis

Biomarker and diagnostic research for arrhythmogenic right ventricular cardiomyopathy has been reported in the published literature.

Prognosis

Estimated prevalence: 1-5 in 10,000 (Uncommon).

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

18 clinical trials registered, 13 recruiting. Interventions under study include other interventions, drug therapy, gene therapy, and procedural interventions. Pipeline includes 2 PHASE2, 1 PHASE1, 4 NA. Research is sponsored by a mix of industry and academic institutions.

NCT ID	Title	Phase	Sponsor	Status
[NCT06546137](https://clinicaltrials.gov/study/NCT06546137)

Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 5:20 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:247

GARD

Genetic and Rare Diseases Info Center

GARD:5847

Questions for Your Care Team

→Are any of the 18 active clinical trials a good fit for my situation?
→Are there specialists or centers of excellence for this condition in my area?
→Is there a patient registry I should consider joining?

← Back to All Diseases

Research Type	Count	% of Total
Research summaries	72	24%
Patient case studies	63	21%
Laboratory research	41	14%
Testing and diagnosis research	38	13%
Disease patterns and progression	36	12%
Clinical study results	21	7%
Other research	18	6%
New treatment approaches	8	3%

arrhythmogenic right ventricular cardiomyopathy

Overview

Diagnosis

Prognosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Subtypes

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications