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Open-label, Dose Escalation Study of Safety and Preliminary Efficacy of TN-401 in Adults With PKP2 Mutation-associated ARVC

Plain-language summary

This study evaluates TN-401, a gene therapy, for its safety and preliminary efficacy in adults with arrhythmogenic right ventricular cardiomyopathy associated with a PKP2 gene mutation. It enrolls adults aged 18 and older who carry a pathogenic PKP2 mutation, have preserved left ventricular function, and have a functioning implantable cardiac defibrillator. The study is in Phase 1 and is currently recruiting participants.

The summary above is a plain-language rendering of the official record. The original English title is shown for reference.

Trial details

Phase
Phase 1
Status
Recruiting
Sponsor
Tenaya Therapeutics
Intervention
TN-401
Start date
3/26/2024
Estimated completion
10/1/2029
Countries
United States

Related genes

Locations

  • San Francisco, United States
  • Aurora, United States
  • Baltimore, United States
  • Boston, United States
  • Rochester, United States
  • New York, United States
  • Cleveland, United States

Eligibility criteria

Criteria are reproduced from the ClinicalTrials.gov record in the original English. Only the trial team can determine eligibility.

Inclusion Criteria:

* PKP2 mutation (pathogenic or likely pathogenic)
* Arrhythmogenic Right Ventricular Cardiomyopathy as defined by the 2010 revised Task Force Criteria
* Left Ventricular Ejection Fraction ≥50%
* Functioning Implantable Cardiac Defibrillator with remote integration capabilities at least 9 months prior to Screening
* NYHA Functional Class I, II, or III
* Frequent premature ventricular contractions (PVCs)

Exclusion Criteria:

* Ventricular tachycardia (VT) ablation within 6 months of Screening or planned VT ablation within 6 months after Screening
* High AAV9 neutralizing antibody titer
* Prior myocardial infarction
* Right Ventricular Heart Failure
* Class IV Heart Failure
* Clinically significant renal disease
* Clinically significant liver disease
This is not medical advice. Consult your specialist.
View the official record on ClinicalTrials.gov →