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Clinical Trials

Elexacaftor/Tezacaftor/Ivacaftor improves CFTR activity and pulmonary function in Cystic Fibrosis Patients carrying the N1303K Mutation

  • Read more about Elexacaftor/Tezacaftor/Ivacaftor improves CFTR activity and pulmonary function in Cystic Fibrosis Patients carrying the N1303K Mutation

People with CF who take part in clinical trials do not represent the general CF population well

  • Read more about People with CF who take part in clinical trials do not represent the general CF population well

Inhaled mRNA therapy for treatment of Cystic Fibrosis: Results of an Early Phase Clinical Trial

  • Read more about Inhaled mRNA therapy for treatment of Cystic Fibrosis: Results of an Early Phase Clinical Trial

Two-year follow-up results from an ongoing study on the safety and effectiveness of elexacaftor/tezacaftor/ivacaftor when used in real-world settings by people with cystic fibrosis

  • Read more about Two-year follow-up results from an ongoing study on the safety and effectiveness of elexacaftor/tezacaftor/ivacaftor when used in real-world settings by people with cystic fibrosis

Willingness of people taking elexacaftor/tezacaftor/ivacaftor to be in new CFTR modulator studies

  • Read more about Willingness of people taking elexacaftor/tezacaftor/ivacaftor to be in new CFTR modulator studies

Outcomes and endpoints reported in studies of pulmonary exacerbations in people with cystic fibrosis (CF): a systematic review

  • Read more about Outcomes and endpoints reported in studies of pulmonary exacerbations in people with cystic fibrosis (CF): a systematic review

Evaluation of a novel compound, AZD5634, in healthy volunteers and patients with cystic fibrosis

  • Read more about Evaluation of a novel compound, AZD5634, in healthy volunteers and patients with cystic fibrosis

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.

Results from a clinical trial of the natural therapeutic alginate OligoG against Burkholderia lung infection in people with cystic fibrosis.

  • Read more about Results from a clinical trial of the natural therapeutic alginate OligoG against Burkholderia lung infection in people with cystic fibrosis.

A new path for CF clinical trials through the use of historical controls

  • Read more about A new path for CF clinical trials through the use of historical controls
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