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Expert Opinion on Orphan Drugs Volume 2, 2014 - Issue 11: Rare Diseases - Detection, Treatment, Care and Research
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Drug Evaluations

Ivacaftor therapy for cystic fibrosis

Susanna A McColleyProfessor of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL, USA;Director, Stanley Manne Children's Research Institute, Clinical and Translational Research, Chicago, IL, USA;Associate Clinical Director of Child Health, Northwestern University Clinical and Translational Sciences Institute, Chicago, IL, USA;Associate Director, Ann and Robert H. Lurie Children's Hospital of Chicago, Cystic Fibrosis Center, Division of Pulmonary Medicine, 225 E. Chicago Avenue, #43, Chicago, IL 60611, [email protected]
, MD
Pages 1225-1232 | Published online: 21 Jul 2014

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Susanna A. McColley. (2016) A safety evaluation of ivacaftor for the treatment of cystic fibrosis. Expert Opinion on Drug Safety 15:5, pages 709-715.
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Susanna A. McColley. (2016) Combination lumacaftor and ivacaftor therapy for cystic fibrosis. Expert Opinion on Orphan Drugs 4:2, pages 233-242.
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Articles from other publishers (1)

Gerhard Laus, Volker Kahlenberg, Sven Nerdinger, Frank Richter & Herwig Schottenberger. (2016) tert -Butyl 3-(3-methyl-1-oxidopyridin-1-ium-2-yl)benzoate . IUCrData 1:1.
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