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September 11, 2024
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CDC data reveal three social drivers that influence suicide risk

Cystic Fibrosis News

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January 02, 2024
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Triple therapy improves chronic rhinosinusitis outcomes in cystic fibrosis

Triple therapy improves chronic rhinosinusitis outcomes in cystic fibrosis

Patients with cystic fibrosis had improved chronic rhinosinusitis outcomes after 1 year of elexacaftor/tezacaftor/ivacaftor therapy, according to results published in JAMA Otolaryngology-Head & Neck Surgery.

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December 27, 2023
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Cystic fibrosis triple therapy safe, tolerable for 144 weeks in older children

Cystic fibrosis triple therapy safe, tolerable for 144 weeks in older children

Elexacaftor/tezacaftor/ivacaftor appeared safe and well tolerated among kids aged 12 years and older with cystic fibrosis and either F508del/minimal function or F508del/F508del genotypes for up to 144 weeks, according to study results.

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September 11, 2024
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CDC data reveal three social drivers that influence suicide risk

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December 04, 2023
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Yearly MRI offers chronic rhinosinusitis monitoring in pediatric cystic fibrosis

Yearly MRI offers chronic rhinosinusitis monitoring in pediatric cystic fibrosis

Yearly paranasal sinus MRI imaging allowed physicians to track chronic rhinosinusitis development in children with cystic fibrosis, according to results published in Annals of the American Thoracic Society.

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November 30, 2023
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FDA grants orphan drug designation to cystic fibrosis treatment

FDA grants orphan drug designation to cystic fibrosis treatment

The FDA granted orphan drug designation to ARCT-032 as a treatment for patients with cystic fibrosis, according to a press release from Arcturus Therapeutics.

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November 27, 2023
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Triple therapy shows safety, tolerability for older children with cystic fibrosis

Triple therapy shows safety, tolerability for older children with cystic fibrosis

In kids aged 6 years and older with cystic fibrosis and either F508del/minimal function or F508del/F508del genotypes, elexacaftor/tezacaftor/ivacaftor was safe and well tolerated for up to 120 weeks, according to study results.

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November 08, 2023
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Aerosol gene therapy safe, heightens CFTR protein levels in cystic fibrosis

Aerosol gene therapy safe, heightens CFTR protein levels in cystic fibrosis

Receipt of 4D-710, an aerosolized gene therapy, resulted in high cystic fibrosis transmembrane conductance regulator protein expression levels in patients with cystic fibrosis, according to a company press release.

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November 03, 2023
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Q&A: Establishing global standard for exercise testing in patients with cystic fibrosis

Q&A: Establishing global standard for exercise testing in patients with cystic fibrosis

For patients with cystic fibrosis, exercise helps with disease management, and exercise tests allow clinicians to assess lung health, muscle strength and treatment response, according to a press release from University of Portsmouth.

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October 02, 2023
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Metals, sulfate in water heighten risk for mycobacterial infections in cystic fibrosis

Metals, sulfate in water heighten risk for mycobacterial infections in cystic fibrosis

Among patients with cystic fibrosis, increases in sulfate and specific metals in water raised the odds for nontuberculosis mycobacterial infections, according to results published in Environmental Epidemiology.

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August 22, 2023
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Late cystic fibrosis care negatively impacts infant weight, height

Late cystic fibrosis care negatively impacts infant weight, height

Infants with cystic fibrosis who received care at 47 days old had decreased weight and height-for-age during infancy compared with infants who received care at 10 days old, according to results published in The Journal of Pediatrics.

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August 16, 2023
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Life expectancy lengthened in recent years for patients with cystic fibrosis

Life expectancy lengthened in recent years for patients with cystic fibrosis

Patients with cystic fibrosis had an average survival of 66 years in 2022, which is a notable increase from 26 years in 2008, according to study results from Epic Research.

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