New England Journal of Medicine · 2018 · 326 citations · 13 references
MedicineMolecular BiologyMolecular GeneticsGene TherapyMolecular DiagnosticsCystic FibrosisCystic Fibrosis PharmacotherapyIon Channel DisordersAdult Cystic Fibrosis PharmacotherapyCftr Gene MutationsCftr Protein FunctionChloride Transport DefectsCystic Fibrosis GeneticsIvacaftor TherapyTezacaftor TherapyTriple Combination Therapy
BACKGROUND: The next-generation cystic fibrosis transmembrane conductance regulator (CFTR) corrector VX-659, in triple combination with tezacaftor and ivacaftor (VX-659-tezacaftor-ivacaftor), was developed to restore the function of Phe508del CFTR protein in patients with cystic fibrosis. METHODS: ). RESULTS: . The sweat chloride concentrations and scores on the respiratory domain of the Cystic Fibrosis Questionnaire-Revised improved in both patient populations. CONCLUSIONS: Robust in vitro activity of VX-659-tezacaftor-ivacaftor targeting Phe508del CFTR protein translated into improvements for patients with Phe508del-MF or Phe508del-Phe508del genotypes. VX-659 triple-combination regimens have the potential to treat the underlying cause of disease in approximately 90% of patients with cystic fibrosis. (Funded by Vertex Pharmaceuticals; VX16-659-101 and VX16-659-001 ClinicalTrials.gov numbers, NCT03224351 and NCT03029455 .).
13
Lutz Nährlich, Jochen G. Mainz, Constantin Adams et al. · Cellular Physiology and Biochemistry · 2013 · 2.5K citations · Full text