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The use of VX-445-tezacaftor-ivacaftor to target Phe508del CFTR protein resulted in increased CFTR function in vitro and translated to improvements in patients with cystic fibrosis with one or two Phe508del alleles. This approach has the potential to treat the underlying cause of cystic fibrosis in approximately 90% of patients. (Funded by Vertex Pharmaceuticals; VX16-445-001 ClinicalTrials.gov number, NCT03227471 ; and EudraCT number, 2017-000797-11 .).
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D. Keating
Gautham Marigowda
Lucy Burr
New England Journal of Medicine
University of Colorado Denver
University of Alabama at Birmingham
University College Dublin
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Keating et al. (Thu,) studied this question.
www.synapsesocial.com/papers/6917e8612bb051071b682b76 — DOI: https://doi.org/10.1056/nejmoa1807120