Paediatrio Ltd

Luminesce Alliance

The Luminesce Alliance is a world-leading paediatric research co-operative, established to harness the strengths of its partner organisations to unlock future prevention, treatments and ultimately, cures, for childhood illnesses. In 2022, the primary focus of the Company was delivering the Centre for Paediatric Precision Medicine research programs that were established with a $20 million investment from NSW Government. The Centre for Paediatric Precision Medicine supported NSW s Paediatric Precision Medicine (PPM) Program which consisted of ten innovative and translational research projects delivered through the Alliance. In addition to this program, there were a further eight NSW Government funded research programs managed and delivered across the Luminesce Alliance they include: Establishment of smallscale cGMP vector manufacturing for gene and cell therapy clinical trials. INFORM2: An exploratory multinational phase I/II combination study of Nivolumab and Entinostat in children and adolescents with highrisk Malignancies. Newborn Screening Program Pilot for SMA and PID in NSW & ACT; A selfamplifying theranostic for treatment of neuroblastoma. Curing genetic metabolic liver disease by precise genomic and epigenomic editing. Translating disease severity biomarkers into the clinic for Rett syndrome. Precision medicine addressing a novel disease pathway to preserve sight in retinal dystrophies. LA Centre for RNA Diagnostics: A pipeline of accredited RNA Diagnostics to extend diagnostic yield of rare disorders by 25 % in 5 years.
33604563680
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NSW 2145
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luminesce.org.au
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LuminesceAlliance
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Amazing work being done by The Luminesce Alliance! It’s inspiring to see such dedication to improving the lives of children with rare diseases and cancers. 💖 #HopeForChildren
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Kudos to all the researchers and families involved! Your stories highlight the importance of precision medicine and making a real difference in the lives of these brave kids. Together, we can create a brighter future! 🌟 #ChildrensHealth
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Poslední diskuze

What role do you think psychosocial support plays in the overall treatment and well-being of children with rare diseases and their families?
Odpovědí: 3, Naposledy před 1 den detail
How can we improve collaboration between researchers, clinicians, and families to enhance outcomes in precision medicine for childhood illnesses?
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NSW 2145
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- H98, H30, H20 -

We support precision medicine research for children with cancer rare diseases and neurodevelopmental disorders. Our outstanding researchers and clinicians are increasing capacity for rare disease research innovation and equitable access to health system support for children with rare diseases and their families. Having a child with a rare complex condition is very isolating says Kris Pierce whose son Will was finally diagnosed with the rare genetic disease SCN2Arelated disorder when he was 14. We can invest millions of dollars but we also need to provide families and healthcare professionals with psychosocial support.

Výzkum pediatrie Výzkum rakoviny Výzkum vrozených vad a genetických onemocnění
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