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We're the largest charity funder of cystic fibrosis research in the UK. Explore some of our recent achievements, made possible by our supporters...
Following formal licensing by the European Commission, clinicians across the UK can now start prescribing the triple combination therapy Kaftrio to eligible people with cystic fibrosis.
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Hundreds of researchers around the world are investigating genetic therapies for cystic fibrosis (CF). Genetic therapies offer the potential of being able to treat everyone with CF, including those who for whatever reason are not eligible for CFTR modulators. Earlier this month we announced funding for a Strategic Research Centre (SRC) grant on developing gene editing therapies, a type of genetic therapy. Here we take a closer look at how gene editing and other types of genetic therapy work and how they could benefit people with cystic fibrosis.
We invest more money into cystic fibrosis research than any other UK organisation.
Find out more about our vision for a life unlimited by cystic fibrosis for everyone with the condition, and our strategy for getting there.
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Discover answers to frequently asked questions about cystic fibrosis.