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About
Survey to be completed independently by HCPs (neurologists treating patients with MS and MS specialist nurses) and patients/caregivers.
Full description
The survey- based study was conducting amongst HCPs and patients/caregivers in selected European countries including Germany, Netherlands, Nordics (Denmark, Sweden), Spain and Croatia, plus Canada, to evaluate whether HCPs and patients/caregivers receive the educational materials and to capture their knowledge of specific Mayzent (siponimod) safety measures.
Enrollment
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Volunteers
Inclusion criteria
Physicians were considered eligible for the survey if they meet the following screening criteria:
Nurses were considered eligible for the survey if they:
Patient inclusion criteria include:
- Had initiated onto Mayzent (siponimod) to treat their MS since reimbursement
Exclusion criteria
-
335 participants in 2 patient groups
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Central trial contact
Novartis Pharmaceuticals; Novartis Pharmaceuticals
Data sourced from clinicaltrials.gov
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