VX-445–Tezacaftor–Ivacaftor in Patients with Cystic Fibrosis and One or Two Phe508del Alleles

D. Keating(German Institute for Economic Research), Gautham Marigowda(German Institute for Economic Research), Lucy Burr(German Institute for Economic Research), Cori Daines(German Institute for Economic Research), Marcus Mall(German Institute for Economic Research), Edward F. McKone(University College Dublin), Bonnie W. Ramsey(German Institute for Economic Research), Steven M. Rowe(German Institute for Economic Research), Laura A. Sass(German Institute for Economic Research), Elizabeth Tullis(German Institute for Economic Research), Charlotte McKee(German Institute for Economic Research), Samuel M. Moskowitz(German Institute for Economic Research), Sarah Robertson(German Institute for Economic Research), J. R. K. Savage(German Institute for Economic Research), C Simard(German Institute for Economic Research), Fredrick Van Goor(German Institute for Economic Research), David Waltz(German Institute for Economic Research), Fengjuan Xuan(German Institute for Economic Research), Timothy Young(German Institute for Economic Research), Jennifer L. Taylor‐Cousar(German Institute for Economic Research)
New England Journal of Medicine
October 18, 2018
Cited by 724Open Access
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Abstract

BACKGROUND: VX-445 is a next-generation cystic fibrosis transmembrane conductance regulator (CFTR) corrector designed to restore Phe508del CFTR protein function in patients with cystic fibrosis when administered with tezacaftor and ivacaftor (VX-445-tezacaftor-ivacaftor). METHODS: ) from baseline. RESULTS: (P<0.001). In both groups, there was a decrease in sweat chloride concentrations and improvement in the respiratory domain score on the Cystic Fibrosis Questionnaire-Revised. CONCLUSIONS: 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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