In a recent issue of CHEST (January 2013), Durmowicz et al 1 highlight the fi nding that despite improvement in both cystic fi bro-sis (CF) transmembrane conductance regulator (CFTR) and pul-monary function in clinical trials of ivacaftor (recently approved by the US Food and Drug Administration for individuals with CF and the G551D mutation), there does not appear to be a direct correlation between changes in sweat chloride (a measure of CFTR function) and changes in FEV 1 (an established effi cacy measure). They also were unable to identify a minimum threshold for change in sweat chloride that was associated with FEV 1 improvement. Despite the fi ndings, lack of a linear correlation between the changes in these outcome measures should not...
Personalized medicine approach in cystic fibrosis (CF) is focusing on detection of cystic fibrosis tra...
International audienceWith the advent of CFTR modulators, surrogate outcome parameters that accurate...
Background Several treatment approaches in cystic fibrosis (CF) aim to correct CF transmembrane cond...
AbstractIvacaftor, a CFTR potentiator that enhances chloride transport by acting directly on CFTR to...
AbstractBackgroundIvacaftor, a cystic fibrosis transmembrane regulator (CFTR) potentiator, decreased...
AbstractBackgroundWe examined data from a Phase 2 trial {NCT00457821} of ivacaftor, a CFTR potentiat...
Introduction: Sweat chloride concentration, a biomarker of CFTR function, is an appropriate outcome ...
Cystic Fibrosis (CF) is a hereditary, systemic disease caused by mutations in the Cystic Fibrosis Tr...
Rationale: Expanding the use of cystic fibrosis transmembrane conductance regulator (CFTR) potentiat...
<div><p>To determine if oral dosing with the CFTR-potentiator ivacaftor (VX-770, Kalydeco) improves ...
To determine if oral dosing with the CFTR-potentiator ivacaftor (VX-770, Kalydeco) improves CFTR-dep...
Objective: To compare differences in epithelial chloride conductance according to class of mutation ...
Aim: The Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) potentiator ivacaftor (Kalydeco®...
textabstractIn patients with cystic fibrosis, cystic fibrosis transmembrane conductance regulator (C...
Ivacaftor is gene-specific oral therapy for patients with cystic fibrosis who have a cystic fibrosis...
Personalized medicine approach in cystic fibrosis (CF) is focusing on detection of cystic fibrosis tra...
International audienceWith the advent of CFTR modulators, surrogate outcome parameters that accurate...
Background Several treatment approaches in cystic fibrosis (CF) aim to correct CF transmembrane cond...
AbstractIvacaftor, a CFTR potentiator that enhances chloride transport by acting directly on CFTR to...
AbstractBackgroundIvacaftor, a cystic fibrosis transmembrane regulator (CFTR) potentiator, decreased...
AbstractBackgroundWe examined data from a Phase 2 trial {NCT00457821} of ivacaftor, a CFTR potentiat...
Introduction: Sweat chloride concentration, a biomarker of CFTR function, is an appropriate outcome ...
Cystic Fibrosis (CF) is a hereditary, systemic disease caused by mutations in the Cystic Fibrosis Tr...
Rationale: Expanding the use of cystic fibrosis transmembrane conductance regulator (CFTR) potentiat...
<div><p>To determine if oral dosing with the CFTR-potentiator ivacaftor (VX-770, Kalydeco) improves ...
To determine if oral dosing with the CFTR-potentiator ivacaftor (VX-770, Kalydeco) improves CFTR-dep...
Objective: To compare differences in epithelial chloride conductance according to class of mutation ...
Aim: The Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) potentiator ivacaftor (Kalydeco®...
textabstractIn patients with cystic fibrosis, cystic fibrosis transmembrane conductance regulator (C...
Ivacaftor is gene-specific oral therapy for patients with cystic fibrosis who have a cystic fibrosis...
Personalized medicine approach in cystic fibrosis (CF) is focusing on detection of cystic fibrosis tra...
International audienceWith the advent of CFTR modulators, surrogate outcome parameters that accurate...
Background Several treatment approaches in cystic fibrosis (CF) aim to correct CF transmembrane cond...