The Ocular Gene and Cell Therapies Australia program is a joint initiative between Sydney Children’s Hospitals Network (SCHN), Children’s Medical Research Institute (CMRI) and Save Sight Institute (SSI), University of Sydney.
The program aims to accelerate the genomic diagnosis and development of novel genetic therapies for children and adults with ocular (eye) diseases across Australia.
The collaborative program is made up of research experts, many of whom are pioneers of their work in various fields, including genomics of genetic ocular diseases, functional investigations, investigation of novel ocular genetic and stem cell therapies, delivery of ocular genetic therapies and clinical expertise in genomic and ophthalmic diagnoses.
The program has gained international recognition for successful work and leadership in genomic and ophthalmic diagnosis and management of Inherited Retinal Diseases (IRD).
The program is now aiming to expand:
- The portfolio of gene and other advanced therapy clinical deliveries and clinical trials
- Translation of multi-omics for additional diagnostic and mechanistic insights in ocular diseases to enhance development of further novel genetic and cellular therapies
- The pre-clinical program to test additional novel gene, stem cell and other advanced therapies for ocular diseases