Cystic fibrosis year in review 2018, part 1
Author:
Affiliation:
1. Department of PediatricsNorthwestern University Feinberg School of MedicineChicago Illinois
2. Stanley Manne Children's Research InstituteChicago Illinois
3. Ann & Robert H. Lurie Children's Hospital of ChicagoChicago Illinois
Publisher
Wiley
Subject
Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ppul.24361
Reference100 articles.
1. Ivacaftor treatment of cystic fibrosis in children aged 12 to <24 months and with a cftr gating mutation (arrival): a phase 3 single‐arm study;Rosenfeld M;Lancet Respir Med,2018
2. Safety, pharmacokinetics, and pharmacodynamics of lumacaftor and ivacaftor combination therapy in children aged 2‐5 years with cystic fibrosis homozygous for f508del‐cftr: An open‐label phase 3 study;McNamara JJ;Lancet Respir Med.,2019
3. Rate and predictors of prescription of lumacaftor ‐ ivacaftor in the 18months following approval in the united states;Sawicki GS;J Cyst Fibros,2018
4. Lumacaftor/ivacaftor in patients with cystic fibrosis and advanced lung disease homozygous for f508del‐cftr;Taylor‐Cousar JL;J Cyst Fibros,2018
5. Tezacaftor/ivacaftor in subjects with cystic fibrosis and f508del/f508del‐cftr or f508del/g551d‐cftr;Donaldson SH;Am J Respir Crit Care Med,2018
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