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Ivacaftor

Reduced levels of nitric oxide in cystic fibrosis airways may be caused by interleukin-1 beta

  • Read more about Reduced levels of nitric oxide in cystic fibrosis airways may be caused by interleukin-1 beta

Tezacaftor/Ivacaftor in Children ≥6 Years of Age With F508del and Residual Function Changes in CFTR.

  • Read more about Tezacaftor/Ivacaftor in Children ≥6 Years of Age With F508del and Residual Function Changes in CFTR.

Wrinkling of the palms on exposure to water in cystic fibrosis patients treated with ivacaftor

  • Read more about Wrinkling of the palms on exposure to water in cystic fibrosis patients treated with ivacaftor

Treatment patterns in people with cystic fibrosis: have they changed since the introduction of ivacaftor?

  • Read more about Treatment patterns in people with cystic fibrosis: have they changed since the introduction of ivacaftor?

Is elexacaftor/tezacaftor/ivacaftor always better than ezacaftor/ivacaftor?

  • Read more about Is elexacaftor/tezacaftor/ivacaftor always better than ezacaftor/ivacaftor?

How does the cystic fibrosis drug ivacaftor move in the body during pregnancy and breastfeeding?

  • Read more about How does the cystic fibrosis drug ivacaftor move in the body during pregnancy and breastfeeding?

New drug for cystic fibrosis does not significantly interfere with another drug that prevents organ rejection

  • Read more about New drug for cystic fibrosis does not significantly interfere with another drug that prevents organ rejection

Infant with cystic fibrosis has normal pancreas function and was missed by newborn screening after mom stayed on CFTR modulator therapy during pregnancy.

  • Read more about Infant with cystic fibrosis has normal pancreas function and was missed by newborn screening after mom stayed on CFTR modulator therapy during pregnancy.

Measuring the impact of CFTR modulation on sweat chloride in cystic fibrosis: Rationale and design of the CHEC-SC Study

  • Read more about Measuring the impact of CFTR modulation on sweat chloride in cystic fibrosis: Rationale and design of the CHEC-SC Study

A phase 3, randomized, double-blind, parallel-group study to evaluate tezacaftor/ivacaftor in people with cystic fibrosis heterozygous

  • Read more about A phase 3, randomized, double-blind, parallel-group study to evaluate tezacaftor/ivacaftor in people with cystic fibrosis heterozygous
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