Clin2
NCT07148739Worth exploringRecruiting

Ensuring Best Access to CF Treatment

Cystic Fibrosis (CF)

Part of Digestive system, Genetic & congenital, Lungs & breathing clinical trials.

This study tests whether people with cystic fibrosis who are already on a triple combination CFTR modulator can stay on their treatment without interruptions or problems. It aims to make sure everyone gets the best, most consistent treatment for their CF.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 4
Enrollment
100 people
Ages
3 years and older
Study type
Interventional

Who can take part

  • You have been diagnosed with cystic fibrosis (CF) and have a known type of CF gene change.
  • You are 2 years old or older.
  • You have been taking a stable dose of a triple combination CFTR modulator (like Trikafta) for at least 2 weeks before the study starts.
  • Your lung disease has been stable—no big drop in lung function or need for extra antibiotics in the past 4 weeks.
  • You can understand and agree to the study procedures, either yourself or with a parent/guardian.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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