lumacaftor and Fibrosis

lumacaftor has been researched along with Fibrosis* in 1 studies

Other Studies

1 other study(ies) available for lumacaftor and Fibrosis

ArticleYear
Profiling the response to lumacaftor-ivacaftor in children with cystic between fibrosis and new insight from a French-Italian real-life cohort.
    Pediatric pulmonology, 2022, Volume: 57, Issue:12

    Clinical trials for CFTR modulators consider mean changes of clinical status at the cohort level, and thus fail to assess the heterogeneity of the response. We aimed to study the different response profiles to lumacaftor-ivacaftor according to age in children with cystic fibrosis (CF).. A mathematical framework, including principal component analysis, data clustering, and data completion, was applied to a multicenter cohort of 112 children aged 6-18 years, treated with lumacaftor-ivacaftor. Studied parameters at baseline and 6 months included body mass index (BMI), number of days of antibiotics (ATB), Sweat test (ST), forced expiratory volume in 1 s expressed in percentage predicted (ppFEV. Change in ppFEV

    Topics: Adolescent; Aminophenols; Aminopyridines; Anti-Bacterial Agents; Benzodioxoles; Child; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Drug Combinations; Fibrosis; Forced Expiratory Volume; Humans; Mutation

2022