ClinicalTrials.Veeva

Menu

A Study to Assess Real-world Patient Characteristics and Clinical Course for Symptomatic Patients With PKP2-ACM (SNAPSHOT- PKP2)

L

Lexeo Therapeutics

Status

Enrolling

Conditions

Arrhythmogenic Cardiomyopathy
PKP2-ACM
PKP2-ARVC

Study type

Observational

Funder types

Industry

Identifiers

NCT06976606
LX2020-03

Details and patient eligibility

About

An observational study to assess real-world patient characteristics and clinical course of disease in participants with PKP2-ACM.

Full description

SNAPSHOT-PKP2 is an observational, multicenter study that consists of 2 parts, a retrospective EMR review (up to 2 years) and a prospective observational study (1 year), to evaluate the clinical burden of illness of patients with PKP2-ACM, and to prospectively evaluate changes in key cardiac parameters and patient-reported outcome measures (PROMs) associated with PKP2-ACM progression.

Enrollment

40 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adults with a clinical diagnosis of ACM as defined by the 2010 revised Task Force Criteria (TFC)
  • Documentation of a pathogenic or likely pathogenic truncating variant in PKP2
  • Frequent premature ventricular contractions (PVCs)
  • Patients must have an ICD placed prior to enrollment
  • Left ventricular ejection fraction (LVEF) ≥ 50% for Part A participants. Left ventricular ejection fraction (LVEF) ≥40% for Part B participants.

Exclusion criteria

  • Evidence of variant(s) in addition to PKP2 that meet standard criteria to be considered pathogenic or likely pathogenic for an arrhythmogenic cardiomyopathy.
  • A history of other cardiac abnormalities as specified in the protocol.
  • New York Heart Association symptoms of heart failure of Class IV at the time of consent.
  • A history of prior gene transfer therapy.

Trial contacts and locations

6

Loading...

Central trial contact

Person*: Lexeo Clinical Trials

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems