New inhaled treatment for children with inherited heart conditions

The project

The project aims to develop a new, non-invasive treatment for children with inherited heart conditions such as hypertrophic cardiomyopathy (HCM). These conditions can cause the heart muscle to thicken, leading to serious health problems from a young age.

Researchers at Curtin are developing a new approach that uses a nebuliser (similar to those used for asthma) to deliver medicine directly to the heart. The treatment uses tiny particles (nanoparticles) to carry genetic medicines designed to help restore normal heart function.

The goal of this research is to create a safer, needle-free treatment option that can be used repeatedly and more comfortably by children and their families.

The involvement opportunity

The research team is looking for 2 consumers to join them. Consumers will:

Skills and experience

The research team are looking for people who:

Other information

Initially, there will be one meeting (1 hour) held online in late April/early May. This discussion will inform a grant application for funding for the project. If the application is successful, there will be an opportunity for ongoing involvement (approximately 2-3 meetings per year).

Applications close 20 April 2026.

Apply now