Viewing Study NCT04895202


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Study NCT ID: NCT04895202
Status: TERMINATED
Last Update Posted: 2023-08-29
First Post: 2021-05-17
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Swiss Study of the Impact of Mayzent on SPMS Patients in a Long-term Non-interventional Study
Sponsor: Novartis Pharmaceuticals
Organization:

Study Overview

Official Title: Swiss Study of the Impact of Mayzent (Siponimod) on Secondary Progressive Multiple Sclerosis Patients in a Long-term Non-interventional Study
Status: TERMINATED
Status Verified Date: 2023-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Insufficient patient recruitment
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: SWISSMASIA
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.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: