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Oxford-Harrington Rare Disease Centre named first global initiative for children with rare disease

November 24, 2023

In the autumn statement on Wednesday 22 November, the government announced its support for the Rare Therapies Launch Pad, a new programme that will develop regulatory pathways for children with rare conditions to access individualised therapies.

The Oxford-Harrington Rare Disease Centre (OHC) in the Department of Paediatrics has a central role in the delivery of this programme, alongside Genomics England, the Association of the British Pharmaceutical Industry and the Medicines and Healthcare Regulatory Agency.

Tens of millions of children globally, including hundreds of thousands in the UK, have rare and life-threatening genetic diseases, with a very small number having access to a treatment. This announcement offers the prospect of change: new individualised therapeutic options are being created but there is currently no route to access these individualised medicines for most patients.

The Launch Pad aims to deliver an end-to-end pathway covering diagnosis, the design and rapid manufacturing of these therapies and treatment.

The programme’s first project will explore the use of individualised therapies called antisense oligonucleotides (ASOs) to treat children with ultra-rare and life-threatening brain conditions. This approach has been driven by Julia Vitarello, mother of Mila, and founder of Mila’s Miracle Foundation. Mila was the first person to receive an individualised medicine, an ASO called Milasen, for a condition called Batten’s disease. Longer term, the Rare Therapies Launch Pad will support access to other types of individualised therapies across a wider range of rare conditions, which affect 1 in 17 people globally.

Oxford-Harrington Rare Disease Centre named in first global. University of Oxford. (n.d.).



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