In the News

The US Food and Drug Administration (FDA) has approved nintedanib (Ofev) oral tablets to treat patients with chronic fibrosing interstitial lung diseases (ILD) with a progressive phenotype. “The FDA continues to encourage the development of therapies for patients with limited or no treatment...
A study of children with cystic fibrosis has identified a test that allows earlier identification of those at risk for cystic fibrosis liver disease. “As we develop new therapies for cystic fibrosis and for other liver diseases, it is critical that we better understand which patients with cystic...
A 3-drug combination of elexacaftor, tezacaftor, and ivacaftor may benefit patients with cystic fibrosis with Phe508del-minimal function genotypes, in whom previous cystic fibrosis transmembrane conductance regulator (CFTR) modulator regimens have been ineffective, according to a study published in...
The US Food and Drug Administration (FDA) has approved the first triple combination therapy to treat patients aged 12 years and older with cystic fibrosis who have at least 1 F508del mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, which is estimated to represent 90...
Patients with cystic fibrosis (CF) who take ivacaftor appear to have fewer respiratory infections over time than those not taking the drug, according to a study published online in the Annals of the American Thoracic Society. The study also showed that ivacaftor may also reduce some of the most...

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