The gene therapy landscape for 

Duchenne muscular dystrophy in Australia.

Join Save Our Sons Duchenne Foundation for a webinar that discusses the gene therapy pipeline for Duchenne muscular dystrophy from an Australian perspective. The webinar will also discuss how clinicians across Australia are working together to support equitable approaches for clinical trial patient recruitment. Presenters will include Dr Ian Woodcock from the Royal Children's Hospital, Melbourne, and Dr Michelle Lorentzos from the Sydney Children's Hospitals Network.

Date: Thursday 29 August 2024

Time: 7:00PM - 8:00PM (AEST)

Hosted by: Save Our Sons Duchenne Foundation



Please fill in your details to register, you will then receive an email with webinar event  zoom link.