Cystic Fibrosis Clinical Trial
Official title:
An Efficacy and Safety Study of Ivacaftor in Patients With Cystic Fibrosis and Two Splicing Mutations
This postmarketing N of 2 study is designed to evaluate the efficacy and safety of open-label ivacaftor treatment in two sisters with cystic fibrosis and pancreatic sufficiency.
The two sisters have a splicing mutation that is predicted to respond favorably to ivacaftor
therapy. In addition to measurement of usual clinical outcomes (i.e. lung function,
nutritional status), there is great interest on the impact on nontuberculous mycobacteria
(NTM) airways infection.
Subjects will undergo sputum cultures at baseline and monthly during treatment, initially in
the absence of anti-NTM therapy but with the intent to treat with antibiotics if there is
persistence of the infection in cultures. Other clinical outcomes will include changes in
sweat chloride, lung function and weight. Safety measures will include periodic assessment of
liver enzymes. All serious and non-serious adverse events will be collected
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