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Allan Scott AO OAM


Women's and Childrens Hospital Foundation


Australian Cystic Fibrosis Research Trust


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Cystic Fibrosis (CF) is the most common inherited disease affecting western society, with one in every 2,500 children being affected.


No cure is available and the current treatments can only (briefly) slow the destruction of the lung. The lung infections in CF patients are extremely difficult to treat, even with the strongest antibiotics and most innovative therapies currently available.


Our research team based at the Women’s and Children’s Hospital in Adelaide has developed a potential cure for CF. Their approach uses gene transfer into the affected airway, to replace the defective gene that causes Cystic Fibrosis.


Cure4CF Foundation was established to support and help fast-track the gene therapy research to the stage of clinical (human) trials. 

Cure4CF Foundation Limited   ABN 71 136 956 137  

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