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NCT06311708Recruiting

Non-interventional Study of Seroprevalence of Pre-existing Antibodies Against Adenovirus-associated Virus Vector (AAV9) and the Progression of Disease in Patients With Plakophilin 2 (PKP2)-Associated Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)

Tenaya Therapeutics

Start Date

1/31/2023

Completion Date

7/11/2030

Summary

This is a multicenter, non-interventional study to observe the natural progression of the disease and to study the prevalence of pre-existing antibodies to AAV9 used for gene therapy in a population of patients with PKP2 gene-associated ARVC. Participation from all patients is encouraged regardless of interest in or eligibility for gene therapy.

Detailed Description

Patients will receive standard of care treatments and assessments under the care of their healthcare provider. Biologic samples will be collected annually to measure cardiac and other related biomarkers. Clinical and observational data will be collected prospectively for up to 5 years from the date of enrollment, or until the patient withdraws consent/assent, undergoes heart transplantation, or dies. If consent is provided, there may be a one-time sample collection to evaluate genetics for research purposes. Quality of Life (QoL) questionnaires will be used to assess a patient's wellbeing and quality of life. If not included as part of a patient's standard of care, diagnostic Holter (or equivalent) monitoring will be required annually. No investigational product will be administered. Participation from all patients is encouraged regardless of interest in or eligibility for gene therapy.

Eligibility Criteria

Age Range: 14 years to 65 years

Inclusion Criteria: * Ages 14-65 years, inclusive, at the time of consent * Pathogenic or likely pathogenic PKP2 gene mutation * Diagnosed with ARVC and meet 2010 Modified Task Force Criteria for ARVC as affected. * Functioning ICD Exclusion Criteria: * Currently receiving systemic immunosuppressive therapy, cytotoxic chemotherapy, immunoglobulin therapy or monoclonal antibody therapy * History of clinically significant liver disease, hepatitis B virus, hepatitis C virus, human immunodeficiency virus, or tuberculosis infection * Previously dosed with any investigational or approved gene therapy product at any time * Concurrent participation in another interventional clinical trial unless approved by the Sponsor. Participation in a noninterventional study may be allowed at the investigator's discretion. * History of cardiac transplant.

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Conditions

Arrhythmogenic Right Ventricular Cardiomyopathy

Locations

University of California San Francisco

San Francisco, California 94143

United States

University of Colorado, Denver

Aurora, Colorado 80045

United States

John Hopkins University School of Medicine

Baltimore, Maryland 21287

United States

Brigham and Women's Hospital

Boston, Massachusetts 02115

United States

Mayo Clinic

Rochester, Minnesota 55905

United States

New York University

New York, New York 10016

United States

Cleveland Clinic

Cleveland, Ohio 44195

United States

Medical University of South Carolina

Charleston, South Carolina 29425

United States

Hopital Louis Pradel

Bron,

France

Nantes University Hospital

Nantes, 44000

France

Pitié-Salpêtrière Hospital

Paris, 75013

France

Hôpital Haut-Lévêque

Pessac, 33604

France

University Hospital Muenster

Münster, 48149

Germany

Wuerzburg University Hospital

Würzburg, 97080

Germany

Centro Cardiologico Monzino

Milan, 20138

Italy

Istituti Clinici Scientifici Maugeri SpA

Pavia,

Italy

Skåne University Hospital

Malmö, 214 28

Sweden

The Queen Elizabeth Hospital

Glasgow, G514TF

United Kingdom

Barts & The London Health NHS Trust

London, E1 1BB

United Kingdom

St. George's University Hospitals NHS Foundation Trust

London, SW17 0QT

United Kingdom

Royal Brompton & Harefield NHS Foundation Trust

London, SW3 6NP

United Kingdom