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| ID | Type | Description | Link |
|---|---|---|---|
| EUPAS104950 | Other Identifier | EU PAS registry |
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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)
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Exjade Prescribers/HCP receiving Educational Materials | HCPs prescribing Exjade in the EU/EEA provided with Exjade Educational Materials |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Physician survey | Other | Survey to assess physicians' knowledge of Exjade posology and biological monitoring recommendations as described in the Educational Materials |
|
| Measure | Description | Time Frame |
|---|---|---|
| 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:
| Through study completion, an average of 6 months. |
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Inclusion Criteria:
Physicians will be required to meet all of the following inclusion criteria:
Exclusion Criteria:
Physicians meeting the following criterion will not be eligible to take the survey:
• Currently employed by a pharmaceutical company, health care company, market research company, advertising agency, or government agency involved in pharmaceutical research or marketing.
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Exjade (deferasirox) prescribers
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| Name | Affiliation | Role |
|---|---|---|
| Novartis Pharmaceuticals | Novartis Pharmaceuticals | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Novartis Investigative Site | Basel | Switzerland |
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