Personalised Treatment For Cystic Fibrosis Patients With Ultra-rare CFTR Mutations (and beyond). KU Leuven
In our HIT-CF project, we aim to bring personalised disease modifying therapies to cystic fibrosis (CF) patients with ultra-rare CFTR mutations, who could otherwise never get access to such treatment. Once we have proven our unique concept, the CF community can easily extend our state-of-the-art methodology to all CF patients such that HIT-CF will impact the entire CF field.
We will achieve our goals by means of a randomised, ...