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Patients completing this 1-year core study were eligible to enter a 4-year extension.
The same pooled sites created in the core study were used in this study.
No comparisons among the initially randomized groups in the core study were performed in this extension study.
Notably, only patients who remained on their randomized medication at the end of the core study were included.
The primary analyses of renal function during the core study were based on the randomized period (months 1 12 posttransplant) by use of last observation carried forward analyses.
Serum ferritin values at the start of deferasirox for patients who received deferasirox during the core study were taken as the mean of all available pretreatment values.
Similar(51)
AEs that occurred during the core study are reported elsewhere.
Patient disposition for the core study was described in the core study manuscript [ 22].
The study design of the core study is described elsewhere [ 22].
The core study was funded by the National Health and Medical Research Council (NHMRC) of Australia.
Details of exclusion criteria for the core study are provided elsewhere [ 22].
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