This study was a retrospective, non-interventional, longitudinal, descriptive study. This study did not have a key underlying hypothesis, rather it was designed to explore the onboarding and adherence of SPMS patients in Australia to Mayzent (siponimod) treatment. Initiating siponimod involves pre-screen tests, including a CYP2C9 genotype test to determine siponimod maintenance dosing, and patients underwent a 6-day titration prior to maintenance. The MSGo platform was developed to support onboarding. It is an integrated digital platform that functions as a patient support service.
Study Type
OBSERVATIONAL
Enrollment
368
Novartis Investigational Site
Camperdown, New South Wales, Australia
Novartis Investigational Site
St Leonards, New South Wales, Australia
Average time for siponimod onboarding
Time frame: Up to 168 days
Time to siponimod onboarding in pre-specified sub-groups
Time frame: Up to 168 days
Percentage of patients who adhered to the titration protocol
Time frame: Up to 168 days
Time on maintenance therapy
Time frame: Up to 168 days
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.