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With the launch of the cystic fibrosis drug Trikafta, about 90% of people with the disease have a treatment. The Cystic Fibrosis Foundation has an ambitious plan to close the gap and go beyond treatments. The nonprofit is committing $500 million to cystic fibrosis drug discovery through 2025, with a focus on not just treating but curing the disease. The funding will mostly support clinical studies of drug classes including mRNA therapy, gene therapy, and gene editing.
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