This study is to assess the pharmacokinetics of deferasirox in hepatically impaired patients compared to healthy volunteers.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
24
one dose of 20 mg/kg/day
Novartis Investigative Site
Kiel, Germany
Pharmacokinetics of deferasirox and its metabolites
Time frame: at FPFV and at LPLV
Safety and tolerability of deferasirox assessed by adverse events
Time frame: at FPFV and at LPLV
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