Rescue Pacing for Congenital Complete Heart Block

This project aims to develop a gene therapy using adenoviral vectors to increase heart rates in fetuses with congenital complete heart block, enabling safe pacemaker implantation post-birth.

Subsidie
€ 150.000
2022

Projectdetails

Introduction

Congenital heart block is the most commonly observed type of foetal bradycardia, occurring in one in 15,000 live births. A significant subset of foetuses develops towards congenital complete heart block (CCHB), i.e., complete failure of the electrical excitation wavefront to be conducted over the atrioventricular (AV) node.

Severity of CCHB

CCHB is the most severe and life-threatening cardiac arrhythmia in utero. Current medicinal treatments cannot significantly alter the cause of CCHB, and therapeutic attempts at human foetal cardiac pacing have been unsuccessful.

Project Objective

For CCHB patients at high risk for life-threatening disease progression and death due to severe bradycardia before 34 weeks of gestation, this project develops a gene therapy medicinal product (GTMP) that is based on adenoviral vector-mediated ion channel overexpression.

Expected Outcomes

The aim is to transiently increase heart rates over the course of several months. When successful, such a GTMP would rescue these patients and allow for permanent pacemaker implantation in the first months after birth.

Financiële details & Tijdlijn

Financiële details

Subsidiebedrag€ 150.000
Totale projectbegroting€ 150.000

Tijdlijn

Startdatum1-8-2022
Einddatum31-1-2024
Subsidiejaar2022

Partners & Locaties

Projectpartners

  • STICHTING AMSTERDAM UMCpenvoerder

Land(en)

Netherlands

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