drugset / Trial / NCT03439865

Ivacaftor for Acquired CFTR Dysfunction in Chronic Rhinosinusitis

NCT03439865

RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this pilot study is to explore wither ivacaftor in refractory CRS patients will demonstrate safety and tolerability; restore CFTR-mediated Cl- secretions as measured by EDSPD testing; produce detectable improvements in validated measures of CRS including the SNOT-22 questionnaire, Lund-MacKay CT scan grading, and Lund-Kennedy endoscopic scores; and provide beneficial effects on readily measured markers of sinonasal inflammation and infection (IP-10, IL-8, and Pseudomonas CFUs).

Timeline

Start
2019-05-02
Primary completion
2027-04
Completion
2027-05-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Ivacaftor Other / unclassified 150 mg Oral