The objective of this survey is to assess the knowledge of HCPs in relation to the recommended posology and biological monitoring for Exjade, based on the current locally valid Exjade educational materials (including the physician's reference checklist)
Study Type
OBSERVATIONAL
Enrollment
400
Survey to assess physicians' knowledge of Exjade posology and biological monitoring recommendations as described in the Educational Materials
Novartis Investigative Site
Basel, Switzerland
Mean percentage of correct responses related to knowledge of posology and biological monitoring recommendations as described in the Exjade EU Summary of Product Characteristics (SmPC)
The primary endpoint is a composite endpoint based on the percentages of HCPs with correct responses to all questions included in the composite regarding the below information: * Administration and dosing of Exjade (deferasirox) FCT * Biological monitoring
Time frame: Through study completion, an average of 6 months.
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