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Brief Title: Swiss Study of the Impact of Mayzent on SPMS Patients in a Long-term Non-interventional Study
Official Title: Swiss Study of the Impact of Mayzent (Siponimod) on Secondary Progressive Multiple Sclerosis Patients in a Long-term Non-interventional Study
Study ID: NCT04895202
Brief Summary: This study is a national, prospective, multicenter, non-interventional (observational) study with the aim to describe the impact of Siponimod treatment in a real-world SPMS population in Switzerland who are treated with Siponimod as per Swiss label.
Detailed Description: Primary data will be collected during an observational period of three years of Siponimod treatment. Additionally, medical history of participants will be collected including EDSS, MRI outcomes, relapses and previous medication to allow the estimation of Siponimod treatment effects on an individual basis. It is planned to include an optional blood draw for a later biomarker analysis.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Novartis Investigative Site, Zug, ZG, Switzerland
Novartis Investigative Site, Zurich, ZH, Switzerland
Novartis Investigative Site, Basel, , Switzerland
Novartis Investigative Site, Bern, , Switzerland
Novartis Investigative Site, Lugano, , Switzerland
Novartis Investigative Site, Winterthur, , Switzerland
Name: Novartis Pharmaceiticals
Affiliation: Novartis Pharmaceuticals
Role: STUDY_DIRECTOR