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Study identifier: NCT07629986 Synced from ClinicalTrials.gov · July 28, 2026
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Pharmacokinetics of Antibiotics in Patients With Cystic Fibrosis Trated With Elexacaftor/Tezacaftor/Ivacaftor (ETI)

Condition: Cystic Fibrosis (CF) · Pulmonary Exacerbation · Respiratory Infection Bacterial  ·  Sponsor: Fondation Ildys

PhaseN/A
Planned participants30
Who can joinAll sexes, 12 Years to no upper limit
Healthy volunteersNo

About this study

Cystic fibrosis (CF) is associated with major pharmacokinetic and pharmacodynamic alterations affecting antibiotic exposure, including changes in absorption, distribution, metabolism, and elimination. Historically, these alterations justified the use of higher antibiotic doses in CF patients in order to achieve therapeutic concentrations and improve pulmonary outcomes. The advent of highly effective CFTR modulators, particularly the triple combination elexacaftor/tezacaftor/ivacaftor (ETI), has substantially improved pulmonary function, nutritional status, inflammatory burden, and quality of life in patients with CF. ETI therapy also appears to modify respiratory microbiology and reduce the frequency of pulmonary exacerbations. These clinical and physiological improvements may alter antibiotic pharmacokinetics and pharmacodynamics in patients with CF, potentially making current high-dose antibiotic recommendations less appropriate for some patients. Since repeated exposure to high-dose antibiotics is associated with cumulative toxicities, particularly aminoglycoside-related ototoxicity and nephrotoxicity, reassessment of antibiotic dosing strategies is warranted. The PKCF study is a multicenter, prospective, observational, non-interventional study designed to characterize the pharmacokinetic profiles of intravenous antibiotics administered during pulmonary exacerbations in adolescents and adults with cystic fibrosis receiving ETI therapy.

This description comes directly from the study's public registry record.

Talk to the study team

Marion Buyse, PharmD, PhD  ·  +33298293447  ·  marion.buyse@ildys.org

Matthieu Pichelin  ·  matthieu.pichelin@ildys.org

Always discuss trial participation with your own doctor first.

Locations (1)

Fondation ILDYSRoscoff, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT07629986