Australian National Duchenne Muscular Dystrophy Registry
The Australian Duchenne Muscular Dystrophy Registry provides an opportunity for Australian DMD patients to participate in clinical trials being undertaken anywhere in the world. The Registry is linked directly to the TREAT-NMD global network of registries, an international effort which has proven effective in improving the health and management of boys with DMD. The Registry provides an important enabling tool for clinicians and clinical trial sponsors to quickly identify patients suitable for each study, particularly those therapeutic strategies that target specific genetic defects.
Potential Benefits of a DMD Registry
Australian DMD Registry Coordinator
|Adding New Patients to Registry|
The database is open to anyone affected by DMD and is entirely voluntary – data obtained is held securely and confidentially. Most of the clinical and genetic information about each patient will be entered locally by the patient’s primary physician in association with the genetic testing laboratories in each state.
Details on how to register can be found on the website
|Please see the website for more information|