Safety and Tolerability of Conversion From Oral, Injectable, or Infusion Disease Modifying Therapies to Dose-titrated Oral Siponimod (Mayzent) in Advancing RMS Patients

Completed · Phase 3

Conditions studied: Multiple Sclerosis, Relapsing Multiple Sclerosis, Advancing Multiple Sclerosis

In brief

To assess safety and tolerability of patients converting from approved Relapsing Multiple Sclerosis (RMS) Disease Modifying Therapies (DMTs) to siponimod.

Key facts

Study ID
NCT03623243
Run by
Novartis Pharmaceuticals
People needed
185
Starts
2019-02-14
Expected to finish
2022-07-06
Last updated by the study team
2024-06-20

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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