Stopped: The study terminated due to low enrollment.
The primary efficacy endpoint of this interventional study was to evaluate the number of patients achieving a complete response (CR), defined as patients switching from intensive deferasirox -DFO treatment, at any time point during the 24 months of study, to deferasirox monotherapy based on improvement in the cardiac magnetic resonance imaging (MRI) T2\* value to \>10ms, and continue to maintain their MRI T2\* to values \>10 msec.
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Number of Patients Achieving a Complete Response (CR)
Timeframe: 24 months
Number of Patients Achieving a Partial Response (PR)
Timeframe: 24 months
Number of Patients With Stable Disease (SD)
Timeframe: 24 months